Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

A V0 core neuronal circuit for inspiration


Breathing in mammals relies on permanent rhythmic and bilaterally synchronized contractions of inspiratory pump muscles. These motor drives emerge from interactions between critical sets of brainstem neurons whose origins and synaptic ordered organization remain obscure. Here, we show, using a virus-based transsynaptic tracing strategy from the diaphragm muscle in the mouse, that the principal inspiratory premotor neurons share V0 identity with, and are connected by, neurons of the preBötzinger complex that paces inspiration. Deleting the commissural projections of V0s results in left-right desynchronized inspiratory motor commands in reduced brain preparations and breathing at birth. This work reveals the existence of a core inspiratory circuit in which V0 to V0 synapses enabling function of the rhythm generator also direct its output to secure bilaterally coordinated contractions of inspiratory effector muscles required for efficient breathing.


In mammals, breathing is a motor behavior generated by a central pattern generator (CPG) located in the brainstem and spinal cord that produces rhythmic contraction of muscles that regulates lung volume and control upper airway patency to maintain bodily homeostasis1. The respiratory CPG in rodents is precociously active in the fetus at around two thirds through gestation2, 3, allowing a period of breathing practice prior to the challenge of encountering air at birth. Starting at birth, the respiratory CPG continuously adapts the frequency and amplitude of the respiratory motor command to metabolic demands linked to exercise and environmental changes. Thus, the respiratory CPG regulates the choice, the timing and the intensity of activation of appropriate groups of premotor neurons, motor neurons, and their muscle targets. The CPG must probably do so respecting two constraints, namely the synchronicity and the balanced amplitude of the motor drives onto left and right respiratory effector muscles (e.g., left and right costal diaphragm muscles that are the prime movers of tidal air). The identity of neurons in charge of securing bilaterally synchronized and amplitude balanced inspiratory motor drive is investigated here.

Over the past decade, strategies exploiting the history of gene expression by neural progenitors or precursors have allowed the manipulation of neurons with unprecedented specificity to reveal their role in circuit function and behavior4, 5. In that way, we established that the preBötzinger complex (preBötC) that paces inspiration6 is composed of interconnected rhythmogenic V0 type neurons (i.e., deriving from p0 progenitors expressing the transcription factor Dbx1), which are synchronized with their contralateral cognate neurons by commissural projections established through the roundabout homolog 3 (Robo3) signaling pathway7. Therefore, bilateral synchronicity of the respiratory motor command is at least in part built-in at the level of the rhythm generator.

Although inspiratory descending circuits have been described for adult rodents and cats8,9,10, nothing is known of the origin of premotor neurons downstream of the rhythm generator that secure temporal and amplitude patterning of the inspiratory motor drive. Here, we addressed this question in early postnatal mice using monosynaptic viral-based circuit-mapping approaches that allow unambiguous identification of phrenic premotor neurons (Ph-preMNs)11. We find that Ph-preMNs are distributed at several sites of the brainstem and include individual neurons with bifurcating axons that connect to phrenic motor neurons (Ph-MNs) on both sides of the midline. The main premotor relay is the rostral ventral respiratory group (rVRG), abutting the preBötC caudally. These rVRG neurons gain prominence over the prenatal period and end up forming at birth, together with the preBötC, the core inspiratory circuit that generates the rhythm and secures bilaterally synchronous and balanced drives to Ph-MNs required for efficient breathing. Strikingly, rVRG and preBötC neurons, found both glutamatergic and harboring commissural axons, share a common origin in p0 progenitors, highlighting the centrality of Dbx1-expressing neural progenitors in the advent of aspiration breathing in vertebrates.


Mapping phrenic premotor neurons in early postnatal mice

To selectively label neurons that synapse onto Ph-MNs, we used transsynaptic rabies technology with monosynaptic restriction. This method makes use of a glycoprotein-G-deleted mutant rabies virus (ΔG-Rb) whose retrograde transsynaptic spread from infected source cells (here Ph-MNs), requires complementation in these cells by the rabies glycoprotein-G (G)11, 12. Once inside presynaptic neurons, the deficient virus ceases to spread for lack of G, and thus only phrenic premotor neurons are traced safe of the confounds normally associated to multi-synaptic jumps of non-deficient rabies virus. ΔG-Rb-mCherry and an adeno-associated virus (AAV) expressing G (AAV-G), were co-injected in the diaphragm of P1 mice (n = 21) to retrogradely infect Ph-MNs and initiate transsynaptic spread to their premotor partners (Fig. 1a). As expected, at P9, Ph-MNs labeled with Rb-mCherry (thereafter trace+) were found in the ventral spinal cord over cervical segments C3-C6 exclusively on the injected side (Fig. 1c). Premotor neurons transsynaptically labeled with mCherry were observed bilaterally in the pons and medulla of the brainstem (Fig. 1b) and in cervical spinal segments, but in no other location. The large majority of Ph-preMNs were found in the rostral ventral respiratory group (rVRG, 399 ± 163 neurons or 70.6 ± 2.7% of all Ph-preMNs, Fig. 1d, m). Others were found in the following locations (Fig. 1m, in decreasing order of abundance; n = 6 mice): the parabrachial nuclei and the Kölliker-Fuse nucleus (PB/KF) in the dorsolateral pons (collectively 51 ± 21 neurons; 9.2 ± 0.6% Fig. 1e); the area of the preBötzinger complex (preBötC, 28 ± 11 neurons; 5.0 ± 0.5% Fig. 1f); the Bötzinger complex (BötC, 21 ± 8 neurons; 3.5 ± 0.4% Fig. 1g); the nucleus of the solitary tract (NTS, 18 ± 7 neurons; 2.7 ± 0.9% Fig. 1h). Other smaller premotor groups were also identified in the brainstem (see Fig. 1g–k) and we aligned serial sections to generate a three-dimensional (3D) reconstruction of all premotor neuronal populations (Fig. 1l; n = 4 mice). Ph-preMNs were not found outside of the brainstem except in the cervical spinal cord in small numbers in laminae VII and X throughout cervical segments C2-C6 (see Supplementary Fig. 3j). Interestingly, the unilateral tracing scheme revealed that the very large majority of Ph-preMNs were found equally distributed on both sides of the midline; only the PB/KF, the NTS and the Gi showed ipsilaterally biased projections (Supplementary Table 1). These observations were confirmed using an alternative method with centrally targeted motor neuron infection to initiate transsynaptic spread (Supplementary Fig. 1).

Fig. 1

Distribution of Ph-preMNs in P9 mice following unilateral viral injections of the diaphragm. a Monosynaptic tracing scheme for Ph-preMNs using a G-deficient Rb virus (ΔG-Rb) and a G-coding adeno-associated (AAV-G) viral cocktail. b, c Brainstem and cervical spinal transverse sections showing, respectively, bilaterally distributed trace+ Ph-preMNs of the rVRG (b) and ipsilaterally located seeding trace+ Ph-MNs. dk Representative images of transverse sections of the brainstem showing (in decreasing abundance order) trace+ Ph-preMNs in the rVRG (d), in the PB/KF (e), in the preBötC (f), in the BötC, Gi and LPGi (g), in the NTS (h), in Ve nuclei (i), in the lRt (j), and in the raphe (k). l 3D reconstructions of the brainstem showing the spatial distribution of Ph-preMNs (n = 4 cumulated counts) in sagittal (top) and horizontal (bottom) views (color code of locations is given in m). m Summary histogram of the distribution Ph-preMNs (percent of total trace+ cells). dmnX, dorsal motor nucleus of the vagus, LRN, lateral reticular nucleus; LVe, lateral vestibular nucleus; MoV, trigeminal motor nucleus; MoXII, hypoglossal motor nucleus; MVe, medial vestibular nucleus; nAc, compact nucleus ambiguus; nAex, external formation of nucleus ambiguus; nAls loose formation of nucleus ambiguus; nAsc, semi-compact nucleus ambiguus; PrV, principal sensory trigeminal nucleus; Spc, spinal cord; SpVe, spinal vestibular nucleus. Scale bars b, c 200 µm; dk 100 µm

To directly visualize the bilateral descending projections of Ph-preMNs, we injected the left diaphragm with a ΔG-Rb-GFP (green) and the right diaphragm with a ΔG-Rb-mCherry (red) (Fig. 2a), both complemented with AAV-G. While, as expected, Ph-MNs exclusively expressed GFP or mCherry, on the left and right side, respectively (Fig. 2c), rVRG neurons and axons were found that co-expressed GFP and mCherry (yellow, Fig. 2b, d, e, f), demonstrating that they individually synapsed onto both, left and right side Ph-MNs (Fig. 2). Such doubly infected neurons were also present in other Ph-premotor areas, the PB/KF (Supplementary Fig. 2a, b), the NTS (Supplementary Fig. 2c), the BötC (Supplementary Fig. 2d) and the preBötC (Supplementary Fig. 2e). Altogether, these data demonstrate that the rVRG hosts neurons with a descending branched axon terminating on Ph-MNs on both sides of the midline (Supplementary Fig. 2f), the simplest cellular design securing synchronous and amplitude balanced motor drives to the left and right diaphragm muscles. As the rVRG outnumbered all other premotor stations by an order of magnitude and contributed to about 70% of all Ph-preMNs, we focused on it for further analysis.

Fig. 2

Individual Ph-preMNs in the rVRG project bilaterally on Ph-MNs. a Tracing scheme based on injections of a green virus (Rb-GFP) in the left diaphragm (L green lettering) and of a red virus (Rb-mCherry) in the right diaphragm (R red lettering). b, c Transverse sections at the level of the rVRG (b) and at the C4 level (c). Note the presence of double labeled (GFP+/mCherry+, yellow) rVRG neurons on the left and right side (b) while seeding Ph-MNs (c) on each side express exclusively either GFP (green) or mCherry (red). df Close-up view of the left (d) and right (e) rVRG showing exclusive green or red cells as well as double labeled cells (yellow). f Close-up view of labeled commissural axons over the midline (dotted line). Scale bars: b, c 200 µm; df 50 µm

Origin and neurotransmitter phenotype of rVRG neurons

With the intention of manipulating rVRG neurons genetically, we next sought to identify their origins as well as their excitatory or inhibitory nature. We performed viral injections for tracing of premotor neurons in diaphragm muscles in mouse lines in which a cre allele is driven by the promoter of the transcription factors Dbx1 (Dbx1 creERT2 ), Engrailed1 (En1 cre), Lbx1 (Lbx1 cre), Sim1 (Sim1 cre ) or of the vesicular glutamate transporter 2 (vGlut2 cre), and vesicular GABA transporter (vGAT cre) using a Tau-nls-lacZ allele as a Cre-dependent reporter. As illustrated in Fig. 3, in the rVRG at P9, about two thirds (range 59.3–77.8%, 65.5 ± 4.2%, n = 4) of trace+ neurons expressed LacZ in a Dbx1 creERT2 background (Fig. 3a), whereas 21.9 ± 1.8% (range 18.3–23.6%, n = 3) did so in a Lbx1 cre background (Fig. 3b) and none did in either the En1 cre or the Sim1 cre background (Supplementary Fig. 3a, b). In addition, we found that trace+ rVRG neurons expressed neither Phox2b (a dB2 marker, Supplementary Fig. 3c) nor Tlx3 (a dB3 marker, Supplementary Fig. 3d). These data indicate that the majority of rVRG neurons originated from Dbx1-expressing ventral progenitors and have thus a V0 identity, while the complement likely originates from dorsal dB1/dB4 progenitor domains marked by expression of Lbx1 but lack of Tlx3 and Phox2b expression13.

Fig. 3

Identity of the Ph-preMNs of the rostral ventral respiratory group. a, b Transverse brainstem section showing trace+ rVRG neurons labeled by Rb-mCherry (red, R) and counterstained for nuclear expression of LacZ (green, Z) and summary histograms featuring the percentage of trace+ rVRG neurons expressing LacZ (yellow bars, RZ). The rVRG is comprised of neurons with a history of expression of Dbx1 (a) or Lbx1 (b). cf Same as above with additional immunostaining for Pax2 (blue, P) and summary histograms showing the percentage of trace+ rVRG neurons expressing LacZ alone (yellow bars, RZ, yellow arrowhead) or co-expressed with Pax2 (white bars, RZP, white arrowhead) when LacZ is expressed from the vGlut2 locus (c); from the vGAT locus (d); from the Dbx1 locus (e) and from the Lbx1 locus (f). Note the comparable proportion of triple positive cells in c, e panels, of double positive cells in d, f panels and the virtual absence of triple positive cells in d, f panels. Scale bars: 50 µm

We found that most (74.7 ± 2.9%, n = 4 mice) trace+ rVRG neurons were excitatory (vGlut2+), among which 90% expressed the transcription factor Pax2 (Fig. 3c), while 17.2 ± 2.5% (n = 4) were inhibitory (vGAT+), all of them lacking Pax2 expression (Fig. 3d). This indicates that Pax2 expression can be used as a proxy for an excitatory phenotype. Pax2 was expressed in 95.8 ± 0.1% (n = 3) of trace- rVRG neurons with V0 identity (Fig. 3e), whereas Pax2 expression was missing in 83.5 ± 2.9% (n = 3) of trace + rVRG neurons with dB identity (Fig. 3f). The inhibitory status of rVRG trace+ neurons recapitulated through Lbx1 cre was confirmed by in situ hybridization to GAD1 and GlyT2 (Supplementary Fig. 3e, f), in agreement with the notion that dB1 and/or dB4 domains are the exclusive providers of inhibitory dB neurons13. Taken together, these findings imply that in the rVRG, neurons with a dB identity contribute the full complement of inhibitory neurons, while the vast majority of neurons are excitatory and have V0 identity.

We next questioned whether other Ph-preMN groups shared V0 identity with the rVRG. The Ph-preMNs located in the PB/KF nucleus (all vGlut2+, data not shown) were fully recapitulated in En1 cre background (Supplementary Fig. 3g) as expected from their known rostral and dorsal rhombencephalic origin14. In the BötC area, Ph-preMNs (all vGAT+, data not shown) were derived from Lbx1-expressing precursors (Supplementary Fig. 3h)15. The Ph-preMNs in the NTS (all vGlut2+, data not shown) expressed Phox2b as expected from their origin in the dA3 domain of progenitors (Supplementary Fig. 3i)16, 17. The only exception in the brainstem was the fraction of trace+ Ph-preMNs located in the preBötC area that also derived from Dbx1-expressing progenitors and were vGlut2+ and Pax2+ but NK1R (Supplementary Fig. 4d–f). These premotor neurons cannot presently be distinguished from rVRG neurons (they could just represent their most rostral contingent) and will be referred to as preBötC Ph-preMNs, only to indicate their location. Occasionally, we noted the presence at spinal level of V0 partition-like cholinergic cells (Supplementary Fig. 3j). Therefore, these data establish that the trace+ glutamatergic Ph-preMNs with V0 identity reside almost exclusively in the rVRG.

Projections of rVRG neurons

To determine whether excitatory rVRG neurons have other synaptic targets in addition to Ph-MNs, we exploited the intense mCherry labeling resulting from monosynaptic retrograde labeling in a Dbx1 creERT2 ; Tau synGFP mouse, where synaptic terminals formed by Dbx1-derived neurons are strongly labeled with synGFP. In this context, the synaptic terminals of trace+ rVRG neurons will be doubly labeled by mCherry and GFP and will be discriminated from those arising from other trace+ premotor groups (mCherry+ only) or V0 trace neurons (GFP+ only). We verified first the massive presence of trace+ rVRG neuron synaptic terminals (7.7 ± 0.52 boutons/soma, n = 62 cells) on motor neurons of the Ph-MN pool (Fig. 4a–c). This contrasted with cranial motor neuron pools that featured fibers and occasional boutons from Ph-preMNs (red), many boutons from trace V0 neurons (green), but virtually no bouton from trace+ rVRG neurons (mCherry+/GFP+, yellow) (Supplementary Fig. 5). Apart from Ph-MNs, the only conspicuous presence of trace+ rVRG synaptic terminals was in the ipsi- and contra-lateral lateral reticular nucleus (LRN), a pre-cerebellar hub structure that also receives ascending signals from multiple spinal premotor sources (Fig. 4g–i)18. In particular, we noted the absence of doubly labeled terminals on trace+ rVRG neurons themselves (0.07 ± 0.04 boutons/soma, n = 54 cells, Fig. 4d–f). Altogether these data indicate that trace+ rVRG neurons are not intrinsically connected and that they send collateral projections to the LRN but not to major respiratory-related cranial motor neurons. In addition, we detected abundant GFP+ only terminals on trace+ rVRG neurons, indicating that they receive inputs from other V0-type neurons that we next set out to identify.

Fig. 4

Synaptic targets of V0 rVRG neurons. a V0 rVRG synaptic terminals double labeled (yellow) by rabies-mCherry (Rb, red) and SynGFP (green) are massively present on Ph-MNs (trace, ChAT+, blue) contralateral to the diaphragm viral injection side. b Zoom on the square inset in a. c Single optical section of the inset in b showing individual synapses (arrowheads). df rVRG (trace+, red) neurons are devoid of double labeled terminals. e Zoom of the inset in d. f Single optical section of the inset in e. g V0 trace+ rVRG neurons project to the lateral reticular nucleus (LRN). h Zoom of the inset in g. i Single optical section of the inset in h showing individual V0 rVRG synaptic terminals (arrowheads) presumably abutting the soma of a LRN neuron. Scale bars: a, d, g 50 µm; b, e, h 20 µm; c, f, i 5 µm

PreBötC V0 neurons connect rVRG V0 neurons

A candidate source of V0 inputs to the rVRG is the preBötC whose neurons form the inspiratory rhythm generator7, 19. To verify this, we modified the original viral tracing scheme to enable an additional retrograde synaptic jump of the ΔG-Rb from V0 neurons. Viral injections were made in Dbx1 creERT2 ; R26 ssHTB pups in which G-complementation and nuclear GFP labeling occurs in V0 neurons thanks to cre-dependent expression of, respectively, G- and histone 2B-GFP-encoding transgenes (Fig. 5a). In this background, the distribution and the number of trace+ neurons in Ph-preMN stations was as in monosynaptic traced pups, but an additional large neuronal population was visualized just anterior to and comparable in size with the rVRG, in the preBötC area (Fig. 5b, c). This neuronal cluster was largely composed of V0 neurons (Fig. 5d–g). These data demonstrate the presence of abundant homotypic V0-V0 synapses between presynaptic preBötC V0 neurons and postsynaptic rVRG V0 neurons.

Fig. 5

V0 homotypic connectivity from the preBötC to the rVRG. a Tracing scheme allowing supplementary retrograde transsynaptic spread from rVRG V0 neurons in Dbx1 creERT2 ; R26 ssHTB pups. b Sagittal sections of the ventral respiratory column showing trace+ neurons (Rb, red) in control (top) and Dbx1 creERT2 ; R26 ssHTB (bottom) pups. Note the presence of an additional trans-synaptically labeled cell population in the PreBötC region (delineated by square corners inset) in Dbx1 creERT2 ; R26 ssHTB. c Summary histograms of the distributions of trace+ neurons in control (black trace, n = 4) and Dbx1 creERT2 ; R26 ssHTB (red trace, n = 4). dg Zoom on the preBötC region (inset in b) of a Dbx1 creERT2 ; R26 ssHTB pup showing trace+ neurons (d) counterstained for GFP (e) and Sst (f) and overlay (g). Arrowheads report trace+ neurons that coexpress GFP and Sst. Scale bars: dg, 50 µm. *p < 0.05

V0 neurons ensure efficient bilateral breathing drives

We then assessed the contribution of synapses made by V0 neurons of the rVRG and preBötC to the mounting of the inspiratory motor drive. First, we tested the ability of rVRG V0 neurons to control the Ph-MNs outputs bilaterally during fetal breathing. At embryonic day (E) 15.5, in brainstem spinal cord preparations (n = 4), a unilateral injection of a rhodamine dextran dye in the phrenic motor column led to bilateral back-labeling of rVRG neurons (Fig. 6a, b) revealing that bilateral descending projections of the rVRG neurons are already established at this stage. We then photo-stimulated the rVRG V0 neurons, in E15.5 Dbx1 creERT2 ; ChR2-tdTomato preparations transversally cut so as to expose the rVRG and eliminate the preBötC (Fig. 6c). In such preparations (n = 5), the phrenic nerves, which exit through the fourth cervical roots (C4) are spontaneously silent. When light was targeted to the rVRG on one side, it activated the ipsi- but not the contra-lateral rVRG and evoked synchronous bilateral bursts of activity on C4 roots (Fig. 6d). Thus, rVRG V0 glutamatergic neurons already transmit their excitation bilaterally to Ph-MNs at the time of inception of fetal breathing.

Fig. 6

Neurons of the rVRG transmit bilaterally their excitation to Ph-MNs at E15.5. a Retrograde tracing scheme in a Dbx1 LacZ/+ brainstem spinal cord at E15.5 using Rhodamine dextran dye unilaterally injected in at C4 level. b Left, transverse slice showing the tracer pattern (red) and LacZ counterstain (green) in the ipsi- and contralateral rVRG (insets) to the tracer injection side. Right, zoom on the insets showing double labeled (yellow) rVRG cells. c Schematic showing the Dbx1 creERT2 ; ChR2-Tdt preparation and unilateral illumination targets (blue empty circles) achieved by computer generated holography outside (1) and on (2) the rVRG while recording activities of left and right C4 motor roots. d Top photostimulation away from the rVRG (blue circle 1 in c) fails both to trigger detectable ∆F/F fluorescence changes and evoke C4 activity responses (right set of traces). Bottom, the light spot positioned on the rVRG (blue circle 2 in c) evokes ∆F/F fluorescence changes restricted to the targeted rVRG (arrowhead) and synchronous left and right C4 bursts (right set of traces). Note that the photostimulation of the rVRG on one side fails to activate the contralateral rVRG. Scale bars: b left, 100 µm; b right, 20 µm

Second, we prevented the commissural navigation of the axons of V0 neurons by deleting the Robo3 gene with a Dbx1 cre line7. In the absence of Robo3 receptor-mediated signaling, axons fail to navigate across the midline20. This conditional interference collectively targets V0 neurons of the preBötC, causing left-right de-synchronization of its activity7, and those of the rVRG, whose role in this context had not been previously investigated. The impairment of the rVRG was attested in Dbx1 cre ; Robo3 lox/lox E15.5 mutants by loss of contralaterally labeled rVRG neurons following a unilateral rhodamine dextran dye injection in the phrenic motor pool (n = 3, Supplementary Fig. 6). To investigate the functional status of this conditional mutant, we monitored the activities of facial motor nucleus (moVII) and phrenic motor output (C4). In wild-type E15.5 brainstem spinal cord preparations, the activities of the moVII and C4 were bilaterally rhythmic and synchronized (Fig. 7a) and the normalized amplitudes of the left and right synchronous bouts of C4 activity were similar (1.02 ± 0.01, n = 77 bursts from five preparations, Fig. 7b). In Dbx1 cre ; Robo3 lox/lox mutants the activities of the moVII were left-right de-synchronized (Fig. 7c) as if receiving only ipsilateral drives from the left-right desynchronized preBötC (Supplementary Fig. 7). Unexpectedly, at the level of the C4 outputs, bilateral synchronization was maintained so that each bout of moVII activity present on either side of the midline was associated with bilaterally synchronized bouts of C4 activity (Fig. 7c). However, the amplitudes of the left or right bouts of C4 activity fluctuated according to the side where the moVII, and thus probably the preBötC, were active (Fig. 7c). The normalized amplitudes of C4 discharges recorded on the active moVII side (ipsi-active) were systematically larger than those recorded from the contralateral (contra) C4, yielding an ipsi-active/contra amplitude ratio of 1.31 ± 0.09 (n = 127 bursts from four preparations, Fig. 7d). These unbalanced left-right C4 amplitudes are, therefore, likely to reflect an excess of descending ipsilateral projections, caused by the conditional Robo3 mutation that translates into a systematic motor overdrive on the side hosting the active preBötC. These experiments confirm the early role of V0 rVRG neurons in the mounting of the inspiratory motor command although, at this stage, commissural premotor neurons other than V0s probably also support the descending inspiratory motor drive. Interestingly, when we repeated these recordings in the same mutant at birth (P0) when physiological breathing needs to operate reliably, we observed a severe worsening of the unbalance of the amplitudes of the left and right C4 outputs. Indeed, the ipsi-active/contra amplitude ratio of C4 activity was dramatically increased to 4.68 ± 0.46 (n = 76 bursts from four preparations, Fig. 7e, f) and for some events contralateral bursts could not be detected.

Fig. 7

V0 neurons ensure bilaterally synchronized and balanced C4 outputs in vitro. a Spontaneous fluorescence (ΔF/F) changes of the left (L) and right (R) facial motor nucleus (VII, top traces) and electrophysiological activities of the left and right C4 motor root (bottom traces) showing phased (*) rhythmic bouts of activity in wild-type preparations. b Histogram of the normalized amplitudes of synchronous left (L C4) and right (R C4) phrenic motor bursts showing their balanced amplitudes. c In Dbx1 cre ; Robo3 lox/lox preparations, the left (black arrowheads) and right (white arrowheads) bouts of VII activity were found de-synchronized but still phased (vertical lines) with bilaterally synchronized bouts of activity of the C4 motor roots. Note the higher amplitude of the burst on the C4 root ipsilateral (ip.C4) to the active VII when compared to that recorded from the contralateral side (Co.C4). d Histogram of the normalized amplitudes of synchronous ip.C4 and Co. C4 showing the reduced amplitude of the latter. e Dbx1 cre ; Robo3 lox/lox mutant preparations, at P0, show an aggravated unbalance of the amplitudes of the synchronous bouts of activity of the left and right C4. f Histogram of the normalized amplitudes of yet synchronous ip.C4 and Co. C4 bursts of activity showing the much greater amplitude of ip.C4 relative to Co. C4 bursts suggesting an almost complete loss of commissural connectivity. Phased activity events (*) were still detected occasionally in Dbx1 cre ; Robo3 lox/lox preparations at both E15.5 (17/144 bursts from four preps) and P0 (6/79 bursts from four preps) either caused by fortuitous phasing of the independent left and right motor drives or by a yet unidentified source of synchronous bilateral drives to the rhythm generator. ***p < 0.001

To check the consequence of commissural V0 axon re-routing on the breathing behavior, we compared plethysmographic recordings of the ventilation in unrestrained wild-type and Dbx1 cre ; Robo3 lox/lox P0 pups (Fig. 8). The mutant pups had atypical ventilation profiles (Fig. 8a, b). First, the distribution of breath durations (T TOT) showed a high incidence of breath separated by abnormally short intervals (Fig. 8c). Furthermore, the distribution of tidal volumes (V T) of the conditional Robo3 null mutants showed a left shift toward small amplitudes breath (Fig. 8d) so that the peak of the V T distribution in the mutant corresponded to about half that of wild-type littermates (5.1 ± 0.4 µl/g, n = 2192 breaths events from eight pups in Dbx1 cre ; Robo3 lox/lox vs. 11.8 ± 0.7 µl/g, n = 3034 breaths events from 13 pups in wild types). This resulted in a left-shifted distribution of the ventilation measurements (V E = V T/T TOT) in the mutant (Fig. 8e) owing to the large fraction of breaths characterized by both low V T and low T TOT values as revealed by density maps of (V T,T TOT) plots (Fig. 8f, g). Altogether, the shallow breathing of the mutants, that mobilized roughly half the lung capacity at about twice a higher frequency, likely results from two freely-running unilateral rhythmic motor commands targeting each a hemi-diaphragm (Supplementary Movie 1). To which extent the decoupled inspiratory drive of the MoVII might contribute to the mutant respiratory distress will need to be investigated further. Asymmetric motor drives to the left and right diaphragm are not compatible with survival, as all Dbx1 cre ; Robo3 lox/lox (13/13) newborn pups died within 24 h like Robo3 null mutants do7, 20.

Fig. 8

Left-right decoupled breathing in Dbx1 cre ; Robo3 lox/lox neonates. a Left, example plethysmographic recordings from three wild-type P0 neonatal pups (#1, #2, #3) during quiet breathing. Right, ten superimposed representative breath (thin lines) and their average (thick line). b Left, comparable recordings for three Dbx1 cre ; Robo3 lox/lox mutant pups. Note the reduced amplitude of breaths and their more frequent occurrence. Right, superimposed representative mutant breaths often appearing as double breath events. ce Summary histograms of the distributions of breath duration (T TOT, c), tidal volumes (V T, d) and ventilation (V E, e) in wild types (black trace), Dbx1 cre ; Robo3 lox/lox (red trace). Note the left shifted distributions for T TOT, V T, and V E in mutants. Stars indicate significant differences with wild types. f, g Density maps of V TT TOT relationships for the breathing of wild types (f) and Dbx1 cre ; Robo3 lox/lox (g). Note in the mutants the high density of aberrant breath featuring both small V T and small T TOT values (in the bottom left quadrant) absent in wild-type pups


An early hypothesis concerning the neural bases of movements by Broadbent in 1866 stated: “That where the muscles of the corresponding parts on opposite sides of the body constantly act in concert, and act independently, either not at all, or with difficulty, the nerve-nuclei of these muscles are so connected by commissural fibres as to be pro tanto a single nucleus.”21. This hypothesis applies well to respiratory movements controlled by “nerve nuclei” with now known origins that include the rhythm generator in the preBötC7, 19, some of its attendant neuro-modulatory control14, 22,23,24 and output Ph-MNs25. Using trans-synaptic tracing strategies we have now revealed the yet uncharted origins of a fourth essential component: phrenic premotor neurons. Among these, the principal premotor neurons that form the rVRG, share V0 identity with, and are synaptic targets of, preBötC neurons. Our data strikingly vindicate and refine the notion that hemi-diaphragms “act in concert” owing to “pro tanto a single nucleus” comprised of V0 type commissural neurons.

Our tracing scheme from the diaphragm restricts the viral spread to premotor neurons11 and thus allowed for the first time a definitive establishment of premotor neurons locations and identities in mouse neonates. Ph-preMNs were exclusively found to reside in the pons and medulla of the brainstem and in the rostral cervical spinal cord. The bulk (about 75%) of brainstem Ph-preMNs locate to the ventral respiratory column in the BötC and, most prominently, in the rVRG. The rest of Ph-preMNs were distributed in the dorsolateral pons in the parabrachial nuclei and Kölliker-Füse nucleus (PB/KF), within the lateral tegmental area in the lateral paragigantocellular (LPGi) and gigantocellular nuclei (Gi), the intermediate reticular nucleus, in vestibular nuclei, in the midline raphe, in the dorsal medulla and in the nucleus of the solitary tract (NTS). Altogether, these locations are in agreement with previous anatomical and electrophysiological delineations of Ph-preMNs made in the adult mouse9, rat8 and cat10, suggesting that inspiratory descending circuits are conserved in mammals and definitively set 1 week after birth. The relatively few Ph-preMNs outside the ventral respiratory column may reflect modulatory roles: integration of viscero- and chemo-sensory afferents in the NTS26, inputs from higher brain centers coordinating various rhythmic motor activities in the PB/KF27, 28 or necessary persistence of breathing during REM sleep atonia through the LPGi29. All these premotor locations featured ipsi-laterally biased projections to Ph-MNs that could introduce an asymmetry of the phrenic premotor drive should they be activated unilaterally. To our knowledge asymmetric volitional breathing has been attested in human patients with vascular hemiplegia30, suggesting that corticospinal descending inputs thought to indirectly project on Ph-MNs31 may target first such premotor neuronal populations.

The part of the ventral respiratory column that extends caudally from the BötC to the rVRG plays the major role in the motorization of the inspiratory pump. It hosts the vast majority of traced Ph-preMNs that are evenly distributed across the midline following unilateral viral injections (Supplementary Table 1). Excitatory and inhibitory Ph-preMNs originate from two distinct sources of progenitors and differentially populate the BötC and the rVRG. Inhibitory vGAT+ Ph-preMNs have a dB1/dB4 origin, form all of the BötC and contribute a third of rVRG neurons, while excitatory vGlut2+ Ph-preMNs by large of p0 origin reside in the rVRG. The few Ph-preMNs located in the area of the preBötC are indistinguishable from rVRG neurons by molecular criteria, suggesting a minor, if any, contribution of the preBötC in the direct transmission of descending drive to Ph-MNs8. Our work identified a fraction of rVRG neurons as inhibitory neurons that together with rVRG excitatory ones may provide concurrent glutamatergic and GABAergic drives to, (i) enable a specific gain control of the Ph-MNs output during inspiration in a BötC-independent manner32, (ii) organize the recruitment of Ph-MNs or smooth out diaphragm force production32, 33. Finally, the inhibitory Ph-preMNs of the BötC are known to provide the synaptic inhibition of Ph-MNs during expiration34.

One major finding is that the predominant premotor group, the glutamatergic rVRG neurons have for the most part V0 identity, like the preBötC. The chief importance, collectively, of these two classes of V0 neurons in breathing coordination is revealed by disrupting their commissures, which caused left-right desynchronized breathing at birth incompatible with survival. The same genetic interference resulted at E15.5 in milder unbalance of left and right C4 drives, showing that the phrenic premotor organization is initially less dependent on V0 cells. Unlike motor behaviors that mature through postnatal incorporation of novel premotor modules35, the inspiratory circuits thus seem to undergo a weeding out of the connectivity outside the preBötC-rVRG module, present at the inception of fetal breathing (this study and ref. 3).

A novel trait, not revealed by traditional tracing methods, is that Ph-preMNs display a special axonal morphology: a bilaterally branched axon synapsing onto phrenic motor pools on both sides of the midline. For technical reasons (see material and methods) these neurons are probably underestimated in our study. Yet, this axonal profile was detected in all of the main phrenic premotor areas: the PB/KF, the NTS, the BötC and in the rVRG. Such a feature has been previously described for components of the premotor circuits that control bilateral whisking35 and jaw closing movements36. Our data indicate that this morphological trait is not related to neuronal origin or subtype identity. Indeed, such neurons were present in premotor stations that originated in dorsal dA, dB domains, in the ventral p0 domain of the neural tube as well as in, necessarily, a fraction only of dA3 subtype neurons of the NTS found with predominant ipsilateral projections. The yet unknown signal that produces axon collateral branching, appears a crucial morphogenetic instruction in several brainstem premotor circuits to ensure the simplest design for bilateral coordination: a single premotor neuron that synapses on equivalent ipsilateral and contralateral motor neurons.

Our tracing experiments also revealed that, collectively, Ph-preMNs send collateral projections to several brainstem visceral and somatic motor nuclei that innervate oro-facial and upper airway patency regulating muscles. However, these projections did not arise from rVRG Ph-preMNs. In fact, axonal terminals of rVRG neurons were only manifest in the LRN, a pre-cerebellar nucleus that, through mossy fibers, relays information from several spinal systems controlling posture, reaching, grasping, and locomotion37. This is consistent with the finding that spinal premotor neurons underpinning voluntary forelimb movements and rVRG premotor neurons directly connect to LRN neurons18. Altogether these findings suggest that the rVRG is the main source of inspiratory corollary discharge38 needed to coordinate breathing with other motor, e.g., postural, locomotor, feeding, expulsive behaviors that rely on partially shared muscles39. Importantly, V0 rVRG axonal terminals were missing in the rVRG itself, a situation strikingly contrasting with preBötC V0 neurons whose intrinsic ipsi- and contra-lateral connectivities ensure rhythm generation and left-right synchronicity.

In sum, our results reveal a core executive control circuit for inspiration comprised of a V0 bilaterally synchronized rhythm generator feeding a V0 bilaterally projecting V0 rVRG premotor station. This redundant architecture alleviates the possibility that asymmetric inputs to this core may translate in unbalanced motor drives to the left and right hemi-diaphragms.

A number of studies hint at the possibility that transcription factors may induce expressing neurons to establish synaptic connections with one another during development, to form neural networks. This may concern Tlx3 40, Brn3a 41, Drg11 42 in the somatic sensory pathways, Atoh1 in proprioceptive pathways43, Lhx6 in an amygdalo-hypothalamic pathway44 and Phox2b in visceral circuits45. V0 neurons in the preBötC and the rVRG recapitulate all of the necessary properties for generation and transmission of the rhythmic inspiratory command in a secured bilaterally synchronized manner to Ph-MNs, for effective muscle contraction powering breathing inflow. Thus, synapses made by neurons sharing a common V0 identity, are sufficient for building an inspiratory motor circuit during development and, in a more speculative way, for the advent of aspiration breathing in tetrapods46.

All extant amniotes draw air in by expanding the thorax (aspiration breathing) as opposed to amphibians, who pump air into the lung by building up pressure in the bucco-pharyngeal cavity47. The amniotes that first evolved a diaphragm required, for its motorization, that respiratory activity be shifted from cranial branchiomotor nerves to spinal somatic ones (e.g., the phrenic nerve), and importantly, that a neural circuit controlling its contractions arose. The present data support an evolutionary scenario whereby these demands may have been met simultaneously. In the spinal cord, V0 neurons were first described as commissural inhibitory premotor neurons synapsing onto somatic motor neurons that innervate hindlimb muscles48. Assuming that this is the default state of V0s produced throughout the neuroaxis, those that are produced in the rVRG (this study) and in the preBötC7 differ from their serial spinal homologues by a glutamatergic phenotype (but see ref. 49). And among those, the latter are rhythmogenic and not premotor, while, as shown here, the former are premotor and not rhythmogenic. We hypothesize that during evolution two neighboring groups of hindbrain commissural premotor V0 neurons simultaneously acquired a glutamatergic phenotype while the rostral group only, the preBötC (possibly through a rhombomere specific-mechanism), acquired the capacity to connect, rather than to motor neurons, to other V0 neurons, i.e., to form homotypic V0-V0 synapses. This would suffice to jointly establish, on the one hand, the preBötC as a rhythm generator whose function relies on the synaptic interconnections of its constitutive V0 neurons according to the group pacemaker hypothesis (ref. 50 and see ref. 1 for a review), and on the other hand, the V0 premotor rVRG as its target. Thus, two subtle V0 fate changes would enable inspiratory rhythm generation and direct its output to Ph-preMNs, thus establishing a redundantly commissural V0 core circuit to secure the bilaterally coordinated contractions of inspiratory pump muscles required for aspiration breathing.


Mouse genetics

The following previously described mouse lines were used in this study: Dbx1 cre (ref. 51), Dbx1 LacZ (ref. 52), Dbx1 creERT2 (ref. 53), En1 cre (ref. 54), Lbx1 cre (ref. 13), Sim1 cre (ref. 55), VGlut2 cre (ref. 56), vGAT cre (ref. 57), ChAT cre (ref. 58), Robo3 lox/lox (ref. 59), RCL-ChR2(H134R)/EYFP abbreviated Ai32 and RCL-hChR2(H134R)/tdT-D abbreviated Ai2760, Tau-lox-stop-lox-Syn-GFP-IRES-nlsLacZpA 61, R26 ssHTB (ref. 62). For recombination induction, Dbx1creERT2 mice were orally gavaged with Tamoxifen (20 mg/ml in corn oil, Sigma) at E10.5 at a dose of 0.1 mg/g of body weight. Live embryos were recovered at E18–E19 through cesarean section, fostered, and raised for further analysis. All animal studies were done in accordance with the guidelines issued by the European Community and have been approved by the research ethics committees in charge (Comité d’éthique pour l’expérimentation animale) and the French Ministry of Research. Sample sizes were chosen on the basis of previous literature. No method of randomization was used to determine how animals were allocated to experimental groups and the investigators were not blinded when analyzing data.

Retrograde tracing experiments

Production of Rb-mCherry, Rb-GFP, and AAV-G for virus experiments with monosynaptic restriction to label premotor neurons were carried out as previously described11, 63. P1 mouse pups of a given Cre-line, were anesthetized by hypothermia, prior to receiving viral injections targeted uni- or bi-laterally to the costal part of diaphragm muscle. Two microliters of a viral solution containing equal volumes of G-deficient rabies virus (titers of ~ 1e + 8) and AAV-G of serotype 6 (titers ~ 3e + 12) were injected in individual muscles. Eight days post injection, P9 pups were deeply anesthetized, transcardially perfused with 4% paraformaldehyde (PFA) in phosphate-buffered saline (PBS), post-fixed overnight in 4% PFA, and cryoprotected in 30% sucrose in PBS and were stored at −80 °C for later immunohistochemistry (IHC). To ascertain that the tracing scheme targeted centrally motor neurons to initiate the viral spread, we compared the distribution of premotor neurons obtained with the above tracing scheme with that resulting from comparable injections using EnvA-pseudotyped ∆G-Rb (titers of ~ 1e + 9) in ChAT cre ; R26 ssHTB animals. The latter tracing scheme was found less effective than the original one. The total number of traced Ph-preMNs (counted in n = 2 experiments) was found reduced by about 35% probably owing to suboptimal viral infection of seeding Ph-MNs in relation to limited cre-dependent expression of TVA from the R26ssHTB allele.

To allow a supplementary retrograde transsynaptic jump of ∆G-Rb from rVRG neurons, we performed unilateral diaphragm injections of viral solution (G-deficient rabies virus and AAV-G) in the Dbx1 creERT2 ; R26 ssHTB genetic background.

Retrograde tracing in E15.5 preparations was performed using pressure injection of Rhodamine dextran MW 3000 (Molecular probes) in the C4 ventral spinal cord of isolated brainstem spinal cord preparations in vitro. After injection, preparations were maintained in the perfusing chamber with the oxygenated (95% O2, 5% CO2) artificial cerebrospinal fluid at RT for 12 h prior to fixation in 4% PFA. Transverse and sagittal 20–60 µm thick sections of the entire brain were performed using a cryostat (Leica CM3050, Germany).

Histology, imaging, and cell counting

The methods for IHC, combined bright field in situ hybridization (ISH) have been described previously7, 23. Gad1 and GlyT2 riboprobes were synthesized using a DIG RNA labeling kit (Roche, Germany) as specified by the manufacturer. And all ISH signals were revealed by NBT and BCIP solution (Roche). Antibodies used for IHC were as follows: Chicken anti-GFP (1/2000, Aves Labs GFP-1020), rabbit anti-GFP (1/2000, Invitrogen A11122), chicken anti-beta-galactosidase (1/2000, Chemicon AB3403), goat anti-ChAT (1/100, Millipore AB144P), rabbit anti-RFP (1/1000 Rockland 600-401-379), rat anti-RFP (1/1000, ChromoTek 5F8), rabbit anti-Pax2 (1/300, Covance PRB-276P), rabbit anti-NK1R (1/5000, Sigma S8305), rabbit anti-Sst (1/500, Peninsula T4103), rabbit anti-Tlx3 (1/5000, kind gift from C. Birchmeier), rabbit anti-Phox2b (kind gift of JF Brunet), mouse anti-Islet1,2 (1/50, DSHB 39.4D5c and 40.2D6c). The primary antibodies were revealed by alexa 488- (Invitrogen, Carlsbad, CA), DyLight 405-, Cy3-, alexa 594-, DyLight 649-, or Cy5-labeled (Jackson Immunoresearch, Suffolk, UK) secondary antibodies of the appropriate specificity. Slides were visualized using a Leica SP8 confocal microscope.

The virally infected premotor neurons were carefully surveyed in the entire brain rostral to the spinal cord. Neurons were counted on both sides in all 1:1 serial sections. Results are expressed as mean ± SEM. The number of traced Ph-preMNs was variable (range: 401–792 neurons; 577 ± 62 neurons, n = 6) from one injection to the other but the relative abundance of neurons in the diverse premotor areas was consistent between experiments. Experiments that resulted in trans-synaptic labeling of less than 150 rVRG neurons (n = 3) failed to label neurons in any other premotor location and were discarded. Neuronal counts in premotor groups are expressed as percentage of the total number of trace+ premotor neurons within the sample. In bilateral diaphragm injection experiments using red and green viruses, the number of doubly labeled premotor neurons is influenced by the probability that primo-infection occurred in pairs of left and right Ph-MNs commonly targeted by a presynaptic partner and by possible competition of the two viral vectors for expression in co-infected cells. This probably introduces an underestimation bias that precluded quantification of Ph-preMNs bearing bilaterally descending branched axons. To quantify secondary viral spread from rVRG neurons in Dbx1 creERT2 ; R26 ssHTB conditional mice while taking into account the inherent variable efficiencies of infections, neuronal counts were expressed as percentage of total number of trace+ rVRG neurons within the sample.

We use the following nomenclature for brainstem structures: rVRG (rostral ventral respiratory group), PB/KF (Parabrachial nuclei and Kölliker-Füse nucleus; given the lack of defined boundaries we pooled lateral and medial subdivision of the parabrachial nucleus), preBötC (preBötzinger complex), BötC (Bötzinger Complex), NTS (nucleus of the solitary tract), LPGi, Gi (Gigantocellular reticular nucleus) Ve (includes vestibular nuclei, medial, lateral and spinal parts), IRt (Intermediate reticular formation), Raphe (includes raphe magnus and obscurus).

Location of the BötC, preBötC and rVRG in neonatal mice

In neonatal mice, at P9, the three subdivisions of the ventral respiratory column: the BötC, preBötC and rVRG, were defined using previously determined anatomical criteria64, 65. From rostral to caudal, the BötC was located caudal to the end of facial motor nucleus (moVII) and ventral to the compact formation of nucleus ambiguus (nAc) (Supplementary Fig. 4a). The preBötC caudal to the BötC and ventral to the semicompact formation of nucleus ambiguus (nAsc), started 300–350 µm caudal to posterior end of moVII (Supplementary Fig. 4b). The rVRG, caudal to preBötC, extended from 550–600 µm caudal to the posterior end of moVII to the rostral pyramidal decussation, ventrally to the loose formation of nucleus ambiguus (nAls), intermingled with the external formation of nucleus ambiguus (nAex) and dorsal to the LRN (Supplementary Fig. 4c).

Digital three-dimensional brainstem reconstructions

The 3D brainstem reconstruction of the virus-labeled premotor neurons was processed as previously described66. Briefly, all sections were acquired with a confocal microscope (Olympus) using a 20× objective. In order to cover the full area of the brainstem with labeled premotor neurons, a mosaic 7 × 5 tile was acquired for each brain section, and stitched by Fiji software. All stitched images were aligned manually using Amira software to construct the 3D model, in which rabies labeled (trace+) premotor neurons were manually assigned (Imaris Spot Detection), and color-coded according to their location based on Paxinos’ mouse brain atlas67.

Calcium imaging, electrophysiology, and photostimulation

The methods used for preparing mouse brainstem–spinal cord preparations from embryonic day 15.5 embryos and P0 mouse and maintaining them in oxygenated artificial cerebrospinal fluid (a-CSF) have been described7, 23, 24. Briefly, brainstem-spinal cord preparations were dissected in 4 °C a-CSF of the following composition (in mM): 128 NaCl, 8 KCl, 1.5 CaCl2, 1 MgSO4, 24 NaHCO3, 0.5 Na2HPO4, 30 glucose, pH 7.4. For calcium imaging of MoVII neurons, brainstem-spinal cord preparations were incubated at room temperature for 40–45 min in oxygenated a-CSF containing the cell-permeable calcium indicator dye Calcium Green-1 AM (10 μM; Life Technologies, Paisley, UK) and were transferred to a recording chamber (30 °C). Optical recordings started after rinsing out for 30 min the excess of dye using a conventional epifluorescence configuration with a FITC filter cube. Fluorescence images were captured from the ventral surface of brainstem-spinal cord preparations exposing the MoVII region, with a cooled Neo sCMOS camera (Andor Technology Ltd., Belfast, UK) using 4× objectives, 4 × 4 binning, an exposure time of 100 ms and for periods of 180 s using Micro-Manager software (

Phrenic nerve activity was recorded on E15.5 and P0 brainstem-spinal cord preparations using suction electrodes positioned on the fourth cervical root (C4) as described7, 23, 24. The raw signals were amplified (High-gain AC, 7P511, Grass Technologies, Warwick, RI), filtered (bandwidth 0.1–3 kHz) and integrated (time constant 50 ms, Integator 7DAEF, Grass Technologies, Warwick, RI) before digital sampling at 6 kHz and analysis using pClamp9 (Molecular Devices). Values are given as mean ± SEM. Statistical significance was tested using a paired difference Student’s t-test to compare the measurements obtained in two different conditions.

In optogenetic experiments, photostimulation was performed using computer generated holography68. Briefly, a 473 nm DPSS laser (CNI, Changchun, China) was used to excite ChR2-expressing neurons. The output beam was expanded to match the input window of a spatial light modulator LCOS-SLM (X10468-01, Hamamatsu), operating in reflection mode. A custom-designed software calculated, given an intensity distribution at the focal plane of the microscope objective, the phase hologram and addressed it to the LCOS-SLM68. The SLM plane was imaged at the back aperture of the microscope objective through a telescope. Individual light pulses of 50 ms duration (laser power density 1–5 mW/mm2) were delivered manually at 7–10 s intervals onto a 100 µm circular region covering the rVRG exposed transversally in E15.5 preparations (Fig. 6c) while recording the electrophysiological activities from the left and right C4 motor roots.

Commissural interference

For Robo3 conditional deletion experiments using Dbx1 creERT2 mice, a single dose of tamoxifen at E10.5 failed to alter bilateral synchrony of activities in the preBötC in transverse slices (data not shown). Extending the treatment to optimize recombination by daily injections over 3 days starting on E9.5 precipitated abortions and yielded altogether only one E15.5 embryo with attested C4 bilateral amplitude unbalance. As tamoxifen treatment, tested in wild-type pregnant females, often resulted in pups showing signs of respiratory distress, we resorted to the use of the non-inducible Dbx1 cre line for both prenatal and P0 functional investigations.

To compare the amplitude of activities recorded from the left and right C4 motor roots in wild-type preparations, we first normalized the amplitude of individual bursts on each side to the mean amplitude of all burst recorded on the corresponding side during the recording period. We then calculated the ratios of the normalized amplitudes of synchronous left and right bursts. To compare the amplitude of C4 activities on either side of the midline in conditional Robo3 null mutants at E15.5, we first normalized the amplitudes of C4 burst on each side to the mean amplitude of all the C4 bursts ipsilaterally co-active with the MoVII (ipsi-active) on the corresponding side. Then the normalized amplitudes of ipsi-active bursts were divided by that of C4 bursts simultaneously recorded on the opposite side (contra) to calculate ipsi-active/contra amplitude ratios. At P0, due to the large unbalance of the amplitudes of left and right C4 bursts, largest peaks were assumed to arise in the ipsi-active side and their amplitude considered as the numerators for calculating ratios.


Breathing variables of un-anesthetized, unrestrained P0 pups were measure by whole-body barometric plethysmography as previously described23. After a 7 min adaptation period in the plethysmograph chamber, the breathing parameters (breath duration (T TOT), tidal volume (V T), and ventilation (V E) calculated as V T/TTOT) were continuously monitored in apnea free periods and scored using a custom software package (Elphy by G Saddoc, Values are given as mean ± SEM. After using F-test to compare the equality of variances, statistical significance was tested using an unpaired difference Student’s t-test to compare data sets obtained from control and mutant pups. Density maps of breath amplitude and duration (V T,T TOT) relationships were obtained using a Python custom made plugin.

Data availability

All relevant data that support the findings of this study are available from the corresponding author upon reasonable request.


  1. 1.

    Feldman, J. L., Del Negro, C. A. & Gray, P. A. Understanding the rhythm of breathing: so near, yet so far. Annu. Rev. Physiol. 75, 423–452 (2013).

    CAS  Article  PubMed  Google Scholar 

  2. 2.

    Greer, J. J., Funk, G. D. & Ballanyi, K. Preparing for the first breath: prenatal maturation of respiratory neural control. J. Physiol. 570, 437–444 (2006).

    CAS  Article  PubMed  Google Scholar 

  3. 3.

    Thoby-Brisson, M., Trinh, J. B., Champagnat, J. & Fortin, G. Emergence of the pre-Botzinger respiratory rhythm generator in the mouse embryo. J. Neurosci. 25, 4307–4318 (2005).

    CAS  Article  PubMed  Google Scholar 

  4. 4.

    Goulding, M. Circuits controlling vertebrate locomotion: moving in a new direction. Nat. Rev. Neurosci. 10, 507–518 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Grillner, S. & Jessell, T. M. Measured motion: searching for simplicity in spinal locomotor networks. Curr. Opin. Neurobiol. 19, 572–586 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  6. 6.

    Smith, J. C., Ellenberger, H. H., Ballanyi, K., Richter, D. W. & Feldman, J. L. Pre-Botzinger complex: a brainstem region that may generate respiratory rhythm in mammals. Science 254, 726–729 (1991).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Bouvier, J. et al. Hindbrain interneurons and axon guidance signaling critical for breathing. Nat. Neurosci. 13, 1066–1074 (2010).

    CAS  Article  PubMed  Google Scholar 

  8. 8.

    Dobbins, E. G. & Feldman, J. L. Brainstem network controlling descending drive to phrenic motoneurons in rat. J. Comp. Neurol. 347, 64–86 (1994).

    CAS  Article  PubMed  Google Scholar 

  9. 9.

    Gaytan, S. P., Pasaro, R., Coulon, P., Bevengut, M. & Hilaire, G. Identification of central nervous system neurons innervating the respiratory muscles of the mouse: a transneuronal tracing study. Brain Res. Bull. 57, 335–339 (2002).

    Article  PubMed  Google Scholar 

  10. 10.

    Onai, T. & Miura, M. Projections of supraspinal structures to the phrenic motor nucleus in cats studied by a horseradish peroxidase microinjection method. J. Auton. Nerv. Syst. 16, 61–77 (1986).

    CAS  Article  PubMed  Google Scholar 

  11. 11.

    Stepien, A. E., Tripodi, M. & Arber, S. Monosynaptic rabies virus reveals premotor network organization and synaptic specificity of cholinergic partition cells. Neuron 68, 456–472 (2010).

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Wickersham, I. R. et al. Monosynaptic restriction of transsynaptic tracing from single, genetically targeted neurons. Neuron 53, 639–647 (2007).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  13. 13.

    Sieber, M. A. et al. Lbx1 acts as a selector gene in the fate determination of somatosensory and viscerosensory relay neurons in the hindbrain. J. Neurosci. 27, 4902–4909 (2007).

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Rose, M. F. et al. Math1 is essential for the development of hindbrain neurons critical for perinatal breathing. Neuron 64, 341–354 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Pagliardini, S. et al. Central respiratory rhythmogenesis is abnormal in lbx1-deficient mice. J. Neurosci. 28, 11030–11041 (2008).

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Dauger, S. et al. Phox2b controls the development of peripheral chemoreceptors and afferent visceral pathways. Development 130, 6635–6642 (2003).

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Storm, R. et al. The bHLH transcription factor Olig3 marks the dorsal neuroepithelium of the hindbrain and is essential for the development of brainstem nuclei. Development 136, 295–305 (2009).

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    Pivetta, C., Esposito, M. S., Sigrist, M. & Arber, S. Motor-circuit communication matrix from spinal cord to brainstem neurons revealed by developmental origin. Cell 156, 537–548 (2014).

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Gray, P. A. et al. Developmental origin of preBotzinger complex respiratory neurons. J. Neurosci. 30, 14883–14895 (2010).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Sabatier, C. et al. The divergent Robo family protein rig-1/Robo3 is a negative regulator of slit responsiveness required for midline crossing by commissural axons. Cell 117, 157–169 (2004).

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Broadbent, W. H. An attempt to remove the difficulties attending the application of Dr Carpenter’s theory of the function of the sensori-motor ganglia to the common form of hemiplegia. BFMCR 37, 468–481 (1866).

    Google Scholar 

  22. 22.

    Li, P. et al. The peptidergic control circuit for sighing. Nature 530, 293–297 (2016).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  23. 23.

    Ruffault, P. L., et al. The retrotrapezoid nucleus neurons expressing Atoh1 and Phox2b are essential for the respiratory response to CO2. eLife 4 e07051 (2015).

    Article  Google Scholar 

  24. 24.

    Thoby-Brisson, M. et al. Genetic identification of an embryonic parafacial oscillator coupling to the preBotzinger complex. Nat. Neurosci. 12, 1028–1035 (2009).

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Philippidou, P., Walsh, C. M., Aubin, J., Jeannotte, L. & Dasen, J. S. Sustained Hox5 gene activity is required for respiratory motor neuron development. Nat. Neurosci. 15, 1636–1644 (2012).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  26. 26.

    Andresen, M. C. & Paton, J. F. in Central Regulation of Autonomic Functions(eds Llewellyn-Smith, I. J. & Verberne, A. J.) 23–46 (Oxford Univ. Press, New York, 2011).

  27. 27.

    Forster, H. et al. Contributions of the pre-Botzinger complex and the Kolliker-fuse nuclei to respiratory rhythm and pattern generation in awake and sleeping goats. Prog. Brain. Res. 209, 73–89 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  28. 28.

    Dutschmann, M. & Dick, T. E. Pontine mechanisms of respiratory control. Compr. Physiol. 2, 2443–2469 (2012).

    PubMed  PubMed Central  Google Scholar 

  29. 29.

    Sirieix, C., Gervasoni, D., Luppi, P. H. & Leger, L. Role of the lateral paragigantocellular nucleus in the network of paradoxical (REM) sleep: an electrophysiological and anatomical study in the rat. PLoS ONE 7, e28724 (2012).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  30. 30.

    Similowski, T., Catala, M., Rancurel, G. & Derenne, J. P. Impairment of central motor conduction to the diaphragm in stroke. Am. J. Respir. Crit. Care Med. 154, 436–441 (1996).

    CAS  Article  PubMed  Google Scholar 

  31. 31.

    Gandevia, S. C. & Rothwell, J. C. Activation of the human diaphragm from the motor cortex. J. Physiol. 384, 109–118 (1987).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  32. 32.

    Parkis, M. A., Dong, X., Feldman, J. L. & Funk, G. D. Concurrent inhibition and excitation of phrenic motoneurons during inspiration: phase-specific control of excitability. J. Neurosci. 19, 2368–2380 (1999).

    CAS  PubMed  Google Scholar 

  33. 33.

    Ellenberger, H. H. & Feldman, J. L. Subnuclear organization of the lateral tegmental field of the rat. I: nucleus ambiguus and ventral respiratory group. J. Comp. Neurol. 294, 202–211 (1990).

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Merrill, E. G. & Fedorko, L. Monosynaptic inhibition of phrenic motoneurons: a long descending projection from Botzinger neurons. J. Neurosci. 4, 2350–2353 (1984).

    CAS  PubMed  Google Scholar 

  35. 35.

    Takatoh, J. et al. New modules are added to vibrissal premotor circuitry with the emergence of exploratory whisking. Neuron 77, 346–360 (2013).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Stanek, E., Cheng, S., Takatoh, J., Han, B. X. & Wang, F. Monosynaptic premotor circuit tracing reveals neural substrates for oro-motor coordination. eLife 3, e02511 (2014).

    Article  PubMed  PubMed Central  Google Scholar 

  37. 37.

    Alstermark, B. & Ekerot, C. F. The lateral reticular nucleus: a precerebellar centre providing the cerebellum with overview and integration of motor functions at systems level. A new hypothesis. J. Physiol. 591, 5453–5458 (2013).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Crapse, T. B. & Sommer, M. A. Corollary discharge across the animal kingdom. Nat. Rev. Neurosci. 9, 587–600 (2008).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  39. 39.

    Bramble, D. M. & Carrier, D. R. Running and breathing in mammals. Science 219, 251–256 (1983).

    ADS  CAS  Article  PubMed  Google Scholar 

  40. 40.

    Logan, C., Wingate, R. J., McKay, I. J. & Lumsden, A. Tlx-1 and Tlx-3 homeobox gene expression in cranial sensory ganglia and hindbrain of the chick embryo: markers of patterned connectivity. J. Neurosci. 18, 5389–5402 (1998).

    CAS  PubMed  Google Scholar 

  41. 41.

    D’Autreaux, F., Coppola, E., Hirsch, M. R., Birchmeier, C. & Brunet, J. F. Homeoprotein Phox2b commands a somatic-to-visceral switch in cranial sensory pathways. Proc. Natl Acad. Sci. USA 108, 20018–20023 (2011).

    Article  PubMed  PubMed Central  Google Scholar 

  42. 42.

    Saito, T., Greenwood, A., Sun, Q. & Anderson, D. J. Identification by differential RT-PCR of a novel paired homeodomain protein specifically expressed in sensory neurons and a subset of their CNS targets. Mol. Cell. Neurosci. 6, 280–292 (1995).

    CAS  Article  PubMed  Google Scholar 

  43. 43.

    Bermingham, N. A. et al. Proprioceptor pathway development is dependent on Math1. Neuron 30, 411–422 (2001).

    CAS  Article  PubMed  Google Scholar 

  44. 44.

    Choi, G. B. et al. Lhx6 delineates a pathway mediating innate reproductive behaviors from the amygdala to the hypothalamus. Neuron 46, 647–660 (2005).

    CAS  Article  PubMed  Google Scholar 

  45. 45.

    Tiveron, M. C., Hirsch, M. R. & Brunet, J. F. The expression pattern of the transcription factor Phox2 delineates synaptic pathways of the autonomic nervous system. J. Neurosci. 16, 7649–7660 (1996).

    CAS  PubMed  Google Scholar 

  46. 46.

    Perry, S. F., Similowski, T., Klein, W. & Codd, J. R. The evolutionary origin of the mammalian diaphragm. Respir. Physiol. Neurobiol. 171, 1–16 (2010).

    Article  PubMed  Google Scholar 

  47. 47.

    Milsom, W. K. Evolutionary trends in respiratory mechanisms. Adv. Exp. Med. Biol. 605, 293–298 (2008).

    Article  PubMed  Google Scholar 

  48. 48.

    Lanuza, G. M., Gosgnach, S., Pierani, A., Jessell, T. M. & Goulding, M. Genetic identification of spinal interneurons that coordinate left-right locomotor activity necessary for walking movements. Neuron. 42, 375–386 (2004).

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Ruder, L., Takeoka, A. & Arber, S. Long-distance descending spinal neurons ensure quadrupedal locomotor stability. Neuron 92, 1063–1078 (2016).

    CAS  Article  PubMed  Google Scholar 

  50. 50.

    Del Negro, C. A. & Hayes, J. A. A ‘group pacemaker’ mechanism for respiratory rhythm generation. J. Physiol. 586, 2245–2246 (2008).

    Article  PubMed  PubMed Central  Google Scholar 

  51. 51.

    Bielle, F. et al. Multiple origins of Cajal-Retzius cells at the borders of the developing pallium. Nat. Neurosci. 8, 1002–1012 (2005).

    CAS  Article  PubMed  Google Scholar 

  52. 52.

    Pierani, A. et al. Control of interneuron fate in the developing spinal cord by the progenitor homeodomain protein Dbx1. Neuron 29, 367–384 (2001).

    CAS  Article  PubMed  Google Scholar 

  53. 53.

    Hirata, T. et al. Identification of distinct telencephalic progenitor pools for neuronal diversity in the amygdala. Nat. Neurosci. 12, 141–149 (2009).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  54. 54.

    Kimmel, R. A. et al. Two lineage boundaries coordinate vertebrate apical ectodermal ridge formation. Genes Dev. 14, 1377–1389 (2000).

    CAS  PubMed  PubMed Central  Google Scholar 

  55. 55.

    Zhang, Y. et al. V3 spinal neurons establish a robust and balanced locomotor rhythm during walking. Neuron 60, 84–96 (2008).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  56. 56.

    Borgius, L., Restrepo, C. E., Leao, R. N., Saleh, N. & Kiehn, O. A transgenic mouse line for molecular genetic analysis of excitatory glutamatergic neurons. Mol. Cell. Neurosci. 45, 245–257 (2010).

    CAS  Article  PubMed  Google Scholar 

  57. 57.

    Vong, L. et al. Leptin action on GABAergic neurons prevents obesity and reduces inhibitory tone to POMC neurons. Neuron 71, 142–154 (2011).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  58. 58.

    Rossi, J. et al. Melanocortin-4 receptors expressed by cholinergic neurons regulate energy balance and glucose homeostasis. Cell Metab. 13, 195–204 (2011).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  59. 59.

    Renier, N. et al. Genetic dissection of the function of hindbrain axonal commissures. PLoS Biol. 8, e1000325 (2010).

    Article  PubMed  PubMed Central  Google Scholar 

  60. 60.

    Madisen, L. et al. A toolbox of Cre-dependent optogenetic transgenic mice for light-induced activation and silencing. Nat. Neurosci. 15, 793–802 (2012).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  61. 61.

    Pecho-Vrieseling, E., Sigrist, M., Yoshida, Y., Jessell, T. M. & Arber, S. Specificity of sensory-motor connections encoded by Sema3e-Plxnd1 recognition. Nature 459, 842–846 (2009).

    ADS  CAS  Article  PubMed  PubMed Central  Google Scholar 

  62. 62.

    Bourane, S. et al. Identification of a spinal circuit for light touch and fine motor control. Cell 160, 503–515 (2015).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  63. 63.

    Tripodi, M., Stepien, A. E. & Arber, S. Motor antagonism exposed by spatial segregation and timing of neurogenesis. Nature 479, 61–66 (2011).

    ADS  CAS  Article  PubMed  Google Scholar 

  64. 64.

    Ellenberger, H. H. Nucleus ambiguus and bulbospinal ventral respiratory group neurons in the neonatal rat. Brain Res. Bull. 50, 1–13 (1999).

    CAS  Article  PubMed  Google Scholar 

  65. 65.

    Ellenberger, H. H. & Feldman, J. L. Brainstem connections of the rostral ventral respiratory group of the rat. Brain. Res. 513, 35–42 (1990).

    CAS  Article  PubMed  Google Scholar 

  66. 66.

    Esposito, M. S., Capelli, P. & Arber, S. Brainstem nucleus MdV mediates skilled forelimb motor tasks. Nature 508, 351–356 (2014).

    ADS  CAS  Article  PubMed  Google Scholar 

  67. 67.

    Paxinos, G. & Franklin, K. B. in The Mouse Brain in Stereotaxic Coordinates 4th edn (Elsevier, 2012).

  68. 68.

    Lutz, C. et al. Holographic photolysis of caged neurotransmitters. Nat. Methods 5, 821–827 (2008).

    CAS  Article  PubMed  PubMed Central  Google Scholar 

Download references


This work was supported by grants from the Agence Nationale de la Recherche (ANR-10-BLAN1410-02 and ANR-32-BSV5-0011-02 to G.F.), Fondation pour la Recherche Médicale (DEQ20120323709 to G.F.), P.C. and S.A. were supported by the Kanton Basel-Stadt, the Novartis Research Foundation, an ERC Advanced Grant and a Swiss National Science Foundation grant, J.W. was supported by fellowships from Fondation pour la Recherche Médicale and from Ecole des Neurosciences de Paris. M.G. was supported by NIH grants NS090919 and NS080586.

Author information




J.W. was involved in design of experiments, carried out experiments, acquired and analyzed data. P.C. performed 3D-reconstructions and produced viral vectors. J.B. and M.G. contributed some of the early data. S.A., G.F. conceived experiments. G.F. supervised the project and wrote the manuscript. All of the authors discussed the results and implications and commented on the manuscript at all stages.

Corresponding author

Correspondence to Gilles Fortin.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Additional information

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Wu, J., Capelli, P., Bouvier, J. et al. A V0 core neuronal circuit for inspiration. Nat Commun 8, 544 (2017).

Download citation

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing