Dysfunctional breathing is the main cause of morbidity and mortality after traumatic injury of the cervical spinal cord1,2 and often necessitates assisted ventilation, thus stressing the need to develop strategies to restore breathing. Cervical interneurons that form synapses on phrenic motor neurons, which control the main inspiratory muscle, can modulate phrenic motor output and diaphragmatic function3,4,5. Here, using a combination of pharmacogenetics and respiratory physiology assays in different models of spinal cord injury, we show that mid-cervical excitatory interneurons are essential for the maintenance of breathing in mice with non-traumatic cervical spinal cord injury, and are also crucial for promoting respiratory recovery after traumatic spinal cord injury. Although these interneurons are not necessary for breathing under normal conditions, their stimulation in non-injured animals enhances inspiratory amplitude. Immediately after spinal cord injury, pharmacogenetic stimulation of cervical excitatory interneurons restores respiratory motor function. Overall, our results demonstrate a strategy to restore breathing after central nervous system trauma by targeting a neuronal subpopulation.
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All quantification data from figures are provided in the Supplementary Information and all raw data are available upon reasonable request.
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This research was supported by grant 2987 from the PVA Research Foundation (M.G.F. and K.S.), CIHR Grant MOP13683 (M.G.F.), AOSPINE Young Investigator Research Grant (K.S.); the Halbert Chair (M.G.F.) and the DeZwirek Foundation (M.G.F.). S.K.K. was supported by the Onassis Foundation. We thank A. Andreopoulou and J. Kallitsis for the ntSCI compression material; J. Austin for logistical support; C. Castro and L. Li for technical assistance; L. Teves (M. Tymianski’s laboratory) for assistance with blood gas measurement. We thank our colleagues for constructive feedback.
Nature thanks J. Feldman and the other anonymous reviewer(s) for their contribution to the peer review of this work.
The authors declare no competing interests.
Publisher’s note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Extended data figures and tables
Extended Data Fig. 1 MRI of the cervical spine of a patient with ntSCI due to degenerative cervical myelopathy.
Arrows point to an area of severe compression of the cervical spinal cord at the C3–C5 levels, the area that houses the PMNs. Of note, this patient did not have clinical respiratory deficits.
a, Sagittal 3D view of a reconstructed cervical spinal cord of a ntSCI mouse extending from C1 (rostral, r) to C8 (caudal, c) demonstrates the compressive injury at C4–C6 spinal level (arrow). b, Cervical spinal cord sections of ntSCI and sham mice stained with haematoxylin and eosin and luxol fast blue (representative of 4 biological replicates). Scale bar, 600 μm.
Representative footprint images from both a mouse (hindpaws only are displayed) and a human ntSCI subject demonstrating decreased stride length and increased base of support during walking relative to control subjects.
a, Representative position–time graph of forepaw movements during skilled walking on a horizontal ladder. b, Bar graph demonstrating an increased number of incorrect forepaw placements as a percentage of total placements in ntSCI mice during ladder walk (P = 0.0012, 95% CI = 16.02 to 39.69). c, Representative image showing reaching and grasping by a ntSCI mouse. d, The number of unsuccessful reaches was greater in ntSCI versus sham mice (P = 0.0025, 95% CI = 5.126 to 15.01). e, The time taken (seconds) to consume a whole length of pasta during the Capellini handling test was increased in ntSCI mice (P = 5.71 × 10−5, 95% CI = 59.06 to 97.21). f, The number of grip adjustments made by the mice during the consumption of the pasta (P = 0.0063, 95% CI = 13.34 to 52.66). Statistical significance was determined using an independent samples two-tailed t-test in b, d–f; n = 3 mice for sham and n = 5 mice for ntSCI. Data are mean ± s.e.m. *P < 0.05.
a, Stacked column graph demonstrating the number of animals with recovered ipsilateral (left) hemidiaphragmatic electromyography (EMG) activity immediately after left C2 hemisection (n = 4 mice per group). Length of compression in the ntSCI animals was related to the proportion of animals with ipsilateral inspiratory activity after C2 hemisection (P = 0.0034, chi-square test for trend). b, Representative EMG recordings from the left hemidiaphragm immediately after left C2 hemisection in sham as well as in 2-, 4- and 8-week ntSCI mice.
Haematoxylin and eosin-stained cervical spinal cord section from a mouse subjected to a left C2 hemisection injury. Scale bar, 600 μm. Staining was performed on 22 separate C2 hemisection samples with similar results.
a, Schematic demonstrating the injection paradigm to assess the anatomical plasticity of the cervical respiratory network after ntSCI. b, c, Bar graphs demonstrating a greater number of cervical interneurons connected to the preserved PMNs (P = 2.0 × 10−4, 95% CI = 96.44 to 183.8, unpaired t-test, two-tailed), and more specifically, a greater number of contralateral cervical interneurons in 8-week ntSCI mice (P = 0.0024, 95% CI = −166.2230 to −40.71032, repeated-measures ANOVA with Sidak’s post hoc test for ipsilateral and contralateral comparisons; n = 3 mice for sham group and n = 5 mice for ntSCI). d, Confocal image of 30-μm-thick transverse cervical spinal cord section demonstrating PRV-traced PMNs on the left (ipsilateral) and prephrenic interneurons in the contralateral ventromedial region; the area where most prephrenic interneurons were located. e, Projections of the PRV152-traced pre-phrenic interneurons to the contralateral area housing the PMNs. Visualization of PRV152 was performed for all samples (n = 3 mice for sham and n = 5 mice for ntSCI) with similar results. Data are mean ± s.e.m. *P < 0.05, **P < 0.001.
High magnification confocal images demonstrate the expression of PSAM (GFP+) in only the excitatory cells (tdTomato+) of the intermediate grey matter. The images were taken from the same sections depicted in Fig. 2c, and are representative of results from 6 biological replicates. Scale bar, 50 μm.
a, Scheme demonstrating the approach used to express hM3Dq–mCherry in the eINs of the intermediate grey matter of C4–C5 spinal level. The Cre-dependent AAV-DIO-hM3Dq-mCherry viral construct was injected in the intermediate grey matter area of the cervical spinal cord of uninjured Vglut2::cre mice (VGLUT2-hM3Dq). b, Representative confocal image demonstrating the expression of hM3Dq–mCherry in the glutamatergic cells of the area of interest (based on 8 biological replicates). Note the lack of expression in the area of motor neurons. CC denotes the central canal. Scale bar, 100 μm. c, Respiratory measurements showed increased inspiratory amplitude but no change in respiratory frequency following stimulation of the cervical eINs (P = 0.9042, repeated-measures ANOVA; n = 8 mice for saline control and CNO groups). The interaction between the change in respiratory amplitude after injection, and treatment (saline versus CNO) was highly significant (P = 0.0002, repeated-measures ANOVA), indicating that the relative change after saline injection is not equal to the relative change after CNO (n = 8 mice for saline control and CNO groups). d, CNO did not change either the inspiratory amplitude (P = 0.3513, paired two-tailed t-test, 95% CI = −0.1077 to 0.04301, n = 9 mice) or the respiratory frequency (P = 0.6906, paired two-tailed t-test, 95% CI = −10.70 to 15.37, n = 9 mice) in Vglut2::cre mice lacking the AAV-DIO-hM3Dq-mCherry injections. e, Representative respiratory activity from VGLUT2-hM3Dq mice before and after saline or CNO administration. f, Representative respiratory activity from Vglut2::cre mice lacking AAV-DIO-hM3Dq-mCherry injection, before and after CNO administration.
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Satkunendrarajah, K., Karadimas, S.K., Laliberte, A.M. et al. Cervical excitatory neurons sustain breathing after spinal cord injury. Nature 562, 419–422 (2018). https://doi.org/10.1038/s41586-018-0595-z
- Inspiratory Amplitude
- Cervical Interneurons
- Phrenic Motoneurons
- Vesicular Glutamate Transporter (VGLUT2)
- Designer Receptors Exclusively Activated By Designer Drugs (DREADD)
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