Astrocytes produce and release L-lactate as a potential source of energy for neurons. Here we present evidence that L-lactate, independently of its caloric value, serves as an astrocytic signalling molecule in the locus coeruleus (LC). The LC is the principal source of norepinephrine to the frontal brain and thus one of the most influential modulatory centers of the brain. Optogenetically activated astrocytes release L-lactate, which excites LC neurons and triggers release of norepinephrine. Exogenous L-lactate within the physiologically relevant concentration range mimics these effects. L-lactate effects are concentration-dependent, stereo-selective, independent of L-lactate uptake into neurons and involve a cAMP-mediated step. In vivo injections of L-lactate in the LC evokes arousal similar to the excitatory transmitter, L-glutamate. Our results imply the existence of an unknown receptor for this ‘glio-transmitter’.
Astrocytes have been implicated in modulation of diverse neuronal circuits1,2,3,4. They influence activity of adjacent neurons in a number of ways, including fine tuning the extracellular K+ concentration1, but by far the best-studied modulatory mechanism involves release of ‘glio-transmitters’—signalling molecules such as ATP5,6, glutamate7 or D-serine8. Yet another mechanism through which astrocytes may affect neuronal activity is commonly referred to as the ‘astrocyte-to-neuron lactate shuttle’9,10,11. In contrast to neurons, astrocytes are ideally poised to serve as a source of L-lactate, as they are capable of storing glucose as glycogen, which they can rapidly mobilize and direct to the glycolytic pathway12,13. This allows for highly dynamic local concentrations of L-lactate. According to the ‘lactate shuttle’ hypothesis, L-lactate released by astrocytes is taken up by neurons via monocarboxylate transporters (MCT) and used as a metabolic substrate, possibly in preference to glucose. Interfering with the ‘shuttle’ using various pharmacological approaches, for example 1,4-dideoxy-1,4-imino-D-arabinitol (DAB), affects long-term potentiation and memory14. The L-lactate stereoisomer, D-lactate (D-lactate) impairs memory in chick, and in the rat, presumably via antagonism with L-lactate14,15. At the same time, there is a considerable body of evidence against the idea that neurons prefer L-lactate to glucose as their energy source12,16. In summary, there is a consensus that astrocytes can release L-lactate upon various stimuli and that L-lactate may affect neuronal function, but the mechanism of L-lactate action remains unclear.
The intimate links between astrocytes and neurons that release norepinephrine (NE) were recognized long ago17,18 but the possibility that astrocytes may control the activity of these neurons and, by doing so, affect brain functions has not been explored. The largest group of NE neurons is the A6 group or locus coeruleus (LC), which supplies NE to the majority of forebrain structures. Interestingly, the input from LC does not only affect neurons but also cortical astrocytes19. The LC has been implicated in control of sleep-wakefulness state, vigilance, appetite, respiration, emotions and autonomic outflows. It may, therefore, be postulated that if astrocytes are able to modulate the activity of LC noradrenergic (NEergic) neurons and affect the release of NE, such a mechanism should have major physiological implications.
Previously, we reported that the astrocytes located on the ventral surface of the medulla oblongata play a role in central chemosensitivity and could be a component of the central homeostate, which maintains constant levels of PCO2/pH4. In that study, we established an optogenetic approach to investigate astrocyte-to-neuron communication using gene expression targeted to either astrocytes or specific neuronal phenotypes. Here, we apply similar strategies to study signalling between astrocytes and LC neurons. We stimulate astrocytes expressing optogenetic actuators with light and measure electrophysiological responses in LC neurons using patch clamp and also directly determine release of NE with fast-scan cyclic voltammetry (FCV). FCV assesses the concentration of NE by measuring its oxidation at a carbon fiber electrode charged to a specific potential. These experiments reveal that L-lactate, released by activated astrocytes or applied by bath, has a powerful excitatory effect on LC neurons, triggering release of NE. Moreover, application of L-lactate to the LC in vivo elicits responses that are qualitatively similar to those evoked by the prototypical excitatory neurotransmitter L-glutamate (GLU). The characteristics of the L-lactate effect on LC neurons may not be explained by its use as a metabolic substrate, but instead support the novel idea that L-lactate acts as a true ‘glio-transmitter’.
L-lactate is involved in astrocyte to neuron signalling in LC
Initially, we used the same in vitro experimental paradigm in cultured slices as in our previous work4 to study interactions between local astrocytes and LC neurons. A few additional tests were performed in primary dissociated cultured astrocytes as specified below. For electrophysiological recordings, astrocytes were transduced with an adenoviral vector (AVV) to express a Channelrhodopsin-2 mutant, ChR2(H134R), fused to red monomeric mKate for visualization (Fig. 1a) or with optoβ2 adrenergic receptors (optoβ2AR), which, upon activation, initiate intracellular signalling cascades similar to those evoked by endogenous astrocytic β2-adrenergic receptors18,20. Qualitatively both optogenetic constructs yielded similar results (Supplementary Fig. 1a–c). ChR2(H134R) was much easier to use in patch clamp experiments probably because of its lower sensitivity to light and hence was used in experiments presented in Fig. 1. NEergic neurons were targeted to express DsRed2 with AVV.sPRSx8.DsRed2 (Fig. 1a). They were visualized using yellow light through confocal optics and recorded in whole-cell mode. Some LC neurons under these conditions were silent, while others showed slow ongoing activity of 1–2 Hz (Figs 1 and 2). Their resting membrane potential was in the same range as previously found in acute slices21,22. Astrocytes then were activated with episodes of flashing 470 nm light. In all cells recorded, optogenetic stimulation of astrocytes evoked depolarization and increased action potential firing of NEergic neurons (Fig. 1b–f). We noted a significant latency of this response (typically over 60 s) and hypothesized that it may reflect recruitment of an enzymatic process and generation of an intermediate such as L-lactate. Indeed, inhibition of L-lactate dehydrogenase by oxamate16 to prevent conversion of pyruvate into L-lactate reversibly prevented light-induced depolarizations (Fig. 1c,f). Blockade of glycogen metabolism with DAB (500 μM)23 had a similar effect (Fig 1d,f). We reasoned that L-lactate produced in response to optogenetic stimulation of glial cells should lead to their intracellular acidification. This was confirmed in pure dissociated astrocytic cultures loaded with the pH indicator SNARF-5AM (Supplementary Fig. 2a). Moreover, such acidification could be prevented by pre-incubation with DAB (500 μM), consistent with involvement of an acidic product of glycogen mobilization. Note that similar results were obtained by activating astrocytes using optoβ2AR (Supplementary Fig. 2b,c)
D-lactate has been used previously to antagonize L-lactate actions in a number of behavioural studies14,15. Bath-applied D-lactate (2 mM) hyperpolarized LC neurons by 5.52±1.65 mV (±s.e.m.; n=6; P=0.0013; Student’s paired t-test; Fig. 1e) and almost completely abrogated depolarizations evoked by activation of astrocytes (Fig. 1e,f). Surprisingly, the MCT inhibitor 4-CIN (100 μM, concentration previously reported to block L-lactate import into central neurons14,24) was unable to prevent neuronal responses to astrocytic activation (Fig. 1f). This prompted us to evaluate effects of exogenously applied L-lactate on the activity of LC neurons.
Exogenous L-lactate is excitatory to LC neurons
Pharmacological analysis of the depolarizing effect of L-lactate is shown in Fig. 2 and summarized in Fig. 3. Bath application of L-lactate (0.2–20 mM; all solutions at pH 7.4) to organotypic slices resulted in reversible depolarization and increased rate of action potential firing in LC neurons, accompanied by marked increases in [Ca2+]i (Fig. 2a,b). The depolarizing effect of L-lactate became significant at 0.2 mM and saturated at concentrations over 6 mM (Fig. 2b) with an apparent EC50 of 680 μM. Of note, [Ca2+]i elevations and depolarizations in LC neurons were preserved in the presence of tetrodotoxin (TTX; 1 μM; Fig. 3; Supplementary Fig. 3). Depolarizations were also unaffected in the presence of a mixture of ionotropic GLU receptor antagonists and a P2 receptor antagonist (CNQX 10 μM, APV 50 μM, MRS2179 10 μM; Figs 2c and 3), indicating that L-lactate excites LC neurons directly. The action of L-lactate was stereo-selective. As in the previous experiments, 2 mM D-lactate hyperpolarized LC neurons and completely occluded the depolarization evoked by 2 mM L-lactate (Figs 2d and 3). D-lactate (200 μM) only slightly hyperpolarized LC neurons (−0.74±0.14 mV, n=3,±s.e.m.; P=0.0328, Student’s paired t-test) but significantly reduced the effect of 2 mM L-lactate (2.63±0.13 mV, n=3, ±s.e.m.; P=0.023, Student’s unpaired t-test; Supplementary Fig. 4a).
Effect of L-lactate on LC neurons is not metabolic
All recorded neurons were patched with pipettes containing 2 mM ATP, 1 mM GTP and 5 mM glucose. The standard perfusion media contained 5.5 mM glucose and varying it between 2 mM and 10 mM had no effect on membrane potential or firing rate of LC cells (Fig. 3; Supplementary Fig. 4b). Under such conditions, it was extremely unlikely that the excitatory effect of L-lactate could be explained by its caloric value.
Several specifically designed experiments consistently demonstrated that the excitatory effect of L-lactate was not due to its uptake by LC neurons and use as an energy substrate. First, pyruvate (2 mM), which can also be transported into the cells by MCT25 and enter the Krebs cycle, had no effect (Figs 2e and 3). Second, when 2 mM L-lactate was added to the patch pipette solution, membrane potential or spiking activity of LC neurons did not change over the period of up to 30 min after establishing whole-cell configuration (Figs 2f and 3). This time was enough to dialyze these neurons as evident from the diffusion of a red fluorescent dye (Fig. 2f inset). However, when the same neurons were later challenged by bath-applied L-lactate, it had a powerful excitatory effect (Fig. 2f). Third, because our recordings are usually performed in HEPES-buffered solution (HBS), we checked whether a switch to a 95% O2/5% CO2 saturated bicarbonate-based artificial cerebrospinal fluid (composition as per26) affects responses to L-lactate. However, the L-lactate effect was similar to the one registered in HBS (bicarbonate-based media: depolarization +6.46±0.75 mV, n=4; in HBS: 6.39±0.75 mV, n=7; ±s.e.m.; P=0.96, Student’s unpaired t-test). Fourth, the MCT blocker 4-CIN (100 μM) had no effect on the ability of L-lactate to activate LC neurons (Fig. 3), consistent with the idea that L-lactate does not need to enter LC neurons to excite them. Acetate (pH 7.4) which is thought to have high membrane permeability and be metabolizable did not mimic the excitatory effect of L-lactate (Fig. 3; Supplementary Fig. 4c).
Together these data suggest that L-lactate is not used by LC neurons as a source of energy but acts on a substrate located on the extracellular side of their plasma membrane to excite them.
Depolarizations are mediated by protein kinase A signalling
L-lactate excites LC neurons without entering them, its effects should require an intracellular second messenger. We therefore tested the involvement of cAMP using an adenylate cyclase (AC) inhibitor, SQ22536 (100 μM) and found that it abolished the depolarizing effect of 2 mM L-lactate (Figs 2g and 3; Supplementary Fig. 4d). Many of the effects of cAMP are mediated by protein kinase A (PKA). The PKA inhibitor H89 (10 μM) suppressed depolarizations, but the phospholipase C (PLC) inhibitor U73122 (10 μM; Fig. 3) had no effect. It has been reported that L-lactate may interfere with uptake of prostaglandins27, leading to their accumulation, which could result in the effects described above. However, pre-incubation of slices with the cyclo-oxygenase inhibitor indomethacin (500 μM) for 30 min (ref. 28) did not significantly alter the effect of L-lactate (Fig. 3).
L-lactate triggers NE release from cultured and acute slices
On the basis of the data described above L-lactate may be expected to stimulate release of NE. This was tested using FCV in organotypic cultured slices cut at the level of the LC (Fig. 4a). To initially confirm that LC neurons release NE upon activation, we expressed in LC neurons an optogenetic actuator ChIEF using AVV.sPRSx8.ChIEF-tdTomato, which also allowed visualization of transgene expressing neurons29,30. Carbon fibre electrodes placed in transduced slices detected clear time-locked increases in NE oxidation currents following trains of blue light pulses (1 ms pulses, 32 Hz for 10 s, power 2–6 mW mm−2). These currents were potentiated by a NE uptake inhibitor desipramine (DES; 500 nM), confirming the catecholamine nature of the signal (Supplementary Figs 5a and 6). The latency of these responses was ~30 s, indicating that the electrodes registered bulk accumulation of extracellular NE, which had to diffuse and possibly cross cellular membranes to reach the electrode.
Bath application of L-lactate (0.2–20 mM) markedly increased NE oxidation currents (Fig. 4b,c). The effect developed within 10–60 s from L-lactate arriving to the slice and was reversible and reproducible. The threshold L-lactate concentration was ~0.2 mM L-lactate, similar to what was found in patch clamp experiments (Fig. 2b). The concentration-response curve predicted an EC50 value of 456 μM (Fig. 4c). The effect of L-lactate was stereo-selective. D-lactate (400 μM) did not trigger NE release but completely blocked the stimulatory action of L-lactate (Fig. 4d). D-lactate (1 μM and 10 μM) shifted the L-lactate concentration-response curve to the right (Fig. 4c) resulting in EC50 of 728 μM (1 μM D-lactate) and 1.133 mM (10 μM D-lactate). TTX (1 μM) only mildly attenuated L-lactate-evoked release of NE (Fig. 4d). Therefore, in addition to somatic depolarization, L-lactate probably has a direct effect on the release machinery, which is partially action potential-independent. Note that, even in the presence of TTX, L-lactate still induced [Ca2+]i elevations and depolarizations in LC neurons (Supplementary Fig. 3).
Consistent with the effect of L-lactate on electrical activity of LC neurons, L-lactate-induced NE release appeared independent of L-lactate caloric value, as pyruvate did not trigger NE release (Fig. 4d) and 4-CIN (100 μM) did not affect L-lactate-induced NE release (Fig. 4d).
AC and PKA mediate L-lactate-evoked NE release
AC inhibition with SQ22536 (100 μM) completely blocked L-lactate-induced NE release (Fig. 4d). A PKA antagonist (H89; 10 μM) also prevented it, in contrast to a PLC blocker, U73122 (10 μM), which did not inhibit L-lactate-induced release of NE (Fig. 4d). Therefore, both the depolarizing effect of L-lactate and L-lactate-induced NE release critically depend on the activity of AC.
L-lactate induces NE release in acute brain slices
To confirm that the ability of L-lactate to induce NE release is not a specific feature of the organotypic slices, which are prepared from young postnatal animals, we confirmed the key observations in acute slices prepared from either 30–33 day old or >2 months old (200–220 g) rats. At both ages L-lactate (400 μM) was a strong stimulant of NE release and the effects appeared greater than in cultured slices (Fig. 4e). Consistent with experiments in slice cultures, D-lactate and SQ22536 blocked the effect of L-lactate, and pyruvate evoked no NE release (Fig. 4e).
Optogenetic activation of astrocytes triggers release of NE
We next tested whether selective activation of astrocytes results in L-lactate-mediated release of NE by LC neurons. In experiments presented below, we stimulated astrocytes using optoβ2AR18,20 (Fig. 4a) but stimulation with ChR2(H134R) yielded similar results (Supplementary Fig. 6).
As mentioned previously, optogenetic activation of astrocytes triggers their acidification via L-lactate production (Supplementary Fig. 2b,c). We then proceeded with the experiments in organotypic-cultured slices where stimulation of optoβ2AR-expressing LC astrocytes with light (20 ms pulses, 16 Hz, 20 s train duration) resulted in a clear increase in NE oxidation currents, which were potentiated by DES (500 nM; Fig. 5; Supplementary Fig. 5b). Release of NE, optogenetically evoked via stimulation of astrocytic optoβ2AR, was abolished by DAB (500 μM, pre-incubated for >5 min), or by oxamate (20 mM; Fig. 5a,d). D-lactate (400 μM), as well as SQ22536 (100 μM), also completely blocked NE release (Fig. 5b–d).
Together these results suggest that activated astrocytes release L-lactate, which, in turn, triggers NE release from LC neurons via a cAMP-dependent signalling mechanism.
Cardiovascular and EEG effects of L-lactate in LC in vivo
On the basis of the previous observations, application of L-lactate to LC may be expected to evoke in vivo effects, which should be comparable to those of an established stimulant, for example GLU. This was tested in anesthetized and artificially ventilated rats. Microinjection of L-lactate (but not vehicle) into the LC evoked significant increases in arterial blood pressure (+13±2 mm Hg, n=11; P=2.9E–05, Student’s paired t-test; Fig. 6a–c). Moreover, L-lactate also evoked a strong increase in the power of high frequency bands of the power spectrum of electro-encephalogram (EEG; Fig. 6d,e). Qualitatively, the effects of L-lactate resembled those of GLU, injected at the same locations (increase in mean arterial blood pressure by 18±3 mm Hg, n=11; P=0.0007, Student’s paired t-test; Fig. 6a,c; EEG changes Fig. 6d,e). Both, L-lactate and GLU evoked variable heart rate changes, which were, however, always unidirectional at the same injection site (Fig. 6a). Injections of GLU outside LC were consistently ineffective as were injections of the buffer in LC or adjacent areas (Supplementary Fig. 7). These data confirm that L-lactate is excitatory to LC neurons in vivo.
Here we demonstrate that exogenous L-lactate excites NEergic neurons in the LC electrically and triggers NE release. We also show that activated astrocytes release L-lactate, which excites adjacent NEergic neurons and stimulates release of NE. The effects of L-lactate are consistent with a role as a ‘glio-transmitter’ and cannot be explained by its use as an energy substrate for LC neurons. Since numerous factors can increase lactate production by astrocytes, this novel signalling pathway could potentially control NE transmission and affect a range of brain functions, which are regulated by inputs from LC (Fig. 7).
Depolarization of LC neurons, which follows optogenetic activation of local astrocytes, was blocked by oxamate or DAB, which prevents formation of L-lactate. D-lactate also blocked astrocyte-induced depolarization of LC neurons. Similarly, DAB, oxamate and D-lactate blocked NE release evoked by the activation of optoβ2AR-expressing astrocytes. Given that activation of astrocytes using either ChR2 or optoβ2AR led to the production of L-lactate (Supplementary Fig. 2) it is logic to conclude that this L-lactate was then released to excite NEergic neurons. Importantly, all the characteristics of the proposed L-lactate-mediated glia-neuronal signalling were consistent with the pharmacology of exogenous L-lactate.
L-lactate, pyruvate and beta-hydroxybutyrate can serve as complimentary fuels for central neurons31,32, but can L-lactate alter neuronal function when energy supply is ample? An earlier study reported excitatory effects of L-lactate on cultured neurons from the embryonic rat brain33, but in these experiments a supra-physiological concentration of L-lactate was used (20 mM) and solutions were not pH balanced, resulting in extra- and intracellular acidification (pH ~4.5). Two further studies reported acute effects of L-lactate on hypothalamic neurons, both supporting L-lactate’s role as a metabolic substrate. First, using patch electrodes containing no glucose and ATP, an excitatory effect of L-lactate on both glucose-inhibited and glucose-excited neurons mediated by via KATP channels was found34. Second, orexin-containing neurons decreased their firing rate after application of 4-CIN, indicating a requirement for L-lactate uptake35. In contrast, all tests conducted in this study consistently demonstrate that the excitatory effects of L-lactate on electrical activity of LC neurons and NE release are not related to use of L-lactate as a complimentary fuel. Conditions of all our experiments are such that neurons can be expected to have abundant sources of energy (high extracellular glucose, glucose and ATP in the pipette solution), and variations of extracellular glucose or level of oxygenation had no effect on the outcome of our tests (Fig. 3). Moreover, when 2 mM L-lactate was dialyzed into LC cells via a patch pipette, the membrane potential was unaffected but extracellular L-lactate was still excitatory (Fig. 2f). This condition should have collapsed or even reversed any inward gradient for L-lactate. Moreover, MCTs co-transport protons together with monocarboxylates and their ability to transport neutralized L-lactate at pH 7.4 must be limited. The high antagonistic efficacy of D-lactate in both patch clamp and NE release experiments is another testimony against the notion that L-lactate acts by entering LC neurons. D-lactate is a poor substrate to all known transporters as compared with L-lactate or pyruvate36,37,38. It follows that D-lactate may not have significantly affected entry of L-lactate into neurons when applied at concentrations 10 or even 100 times less than L-lactate, but nevertheless it powerfully suppressed L-lactate-induced effects. All other facts point in the same direction. Neither pyruvate nor acetate were effective in any of the tests, although both could be used as energy sources. A blocker of MCTs, 4-CIN, was completely ineffective, although in previous studies 4-CIN antagonized energy-mediated effects of L-lactate on orexin neurons35. Taken together, these data provide the first demonstration of a pH- and energy-independent excitatory effect of L-lactate on central neurons.
In both our patch clamp and FCV experiments, the threshold for L-lactate action was close to 0.2 mM. The EC50 of L-lactate was calculated to be 680 μM for patch clamp recordings (Hill slope ~0.7) and 456 μM for NE release. These values match the average physiological range of extracellular L-lactate found in the brain of a healthy rat (0.2–1 mM)39,40, but bursts of activity are likely to trigger steep local L-lactate gradients.
The effects of D-lactate documented here were unexpected and surprising. Indeed, in both patch clamp and FCV experiments, it acted as a potent inhibitor of L-lactate actions (Figs 1e,f, 2d, 3, 4c–e and 5b,d), this being consistent with the idea of D-lactate acting as a receptor antagonist rather than as a competitive substrate for a transporter. Since the excitatory effect of L-lactate does not require its uptake into LC neurons, it is logical to conclude that D-lactate interferes with L-lactate at a receptor site located on the extracellular side of the plasma membrane. Interestingly, in patch clamp experiments, D-lactate caused hyperpolarization suggestive of some basal tone within this signalling pathway under our conditions. In both patch clamp and FCV experiments, blocking AC with SQ22536 prevented the actions of L-lactate, implicating cAMP as a second messenger. Consistent with this idea, the PKA blocker H89 also prevented effects of L-lactate. In contrast, a PLC blocker U73122 was without effect. Because L-lactate-induced release of NE is little affected by TTX, it is possible that NE release evoked by L-lactate is, in part, independent of action potential firing of LC neurons. Previously, we demonstrated using carbon fibre micro-amperometry that TTX attenuates but not abolishes release of NE from identified varicosities of CA neurons in the rat brain41. Our earlier work in adrenal chromaffin cells showed that Ca2+ released from intracellular stores upon second messenger signalling can drive catecholamine release also in absence of depolarizations42. At the same time, NEergic neurons in slices typically have membrane potentials in the range of −50 to −65 mV (refs 21, 22). It is therefore equally possible that even mild depolarizations, which persist in the presence of TTX (as shown in Supplementary Fig. 3), are able to open voltage-gated Ca2+ channels, leading to release of NE, which can additionally be potentiated by cAMP-mediated signalling43.
Finally, in vitro results strongly suggested that application of L-lactate to the LC in vivo should trigger effects consistent with the activation of LC neurons and qualitatively (if not quantitatively) similar to those evoked by a standard excitatory neurotransmitter. Indeed, unilateral GLU and L-lactate into the same locations evoked unidirectional physiological responses, but only when the drugs were placed into LC. The choice of L-lactate dose for microinjection studies was based on the assumption that L-lactate should be used in concentrations/quantities equal or higher than those used for GLU, this being a conservative approach. Indeed, GLU receptors have nanomolar affinity, while our in vitro experiments required micromolar concentrations of L-lactate. At the same time, both molecules are subject to rapid uptake and removal from the site of injection. Both L-lactate and GLU evoked mild increases in blood pressure and triggered the expected changes in the EEG power spectrum with reductions in the low and marked increases in the high frequency bands. These results demonstrate that L-lactate has a profound excitatory effect on the LC.
Taken together, the characteristics of the L-lactate-mediated responses described above suggest the existence of a membrane receptor for L-lactate on LC neurons. However, it is highly unlikely that the hydrocarboxylic acid-1 receptor (HCA-1; previously known as GPR81, GPR104 or LACR1) described in adipose tissue could be responsible. HCA-1 is implicated in regulation of lipid breakdown44,45 and has an EC50 of ~5 mM (ref. 46), which is ~10 times higher than the estimates in the present experiments. Further, D-lactate is a weak agonist at HCA-1, while in our experiments it acted as antagonist or inverse agonist. The intracellular coupling mechanism of HCA-1 (GPR81) is incompatible with the effects described here as all published studies consistently demonstrated HCA-1 coupling to Gi proteins44,45,46,47. In neurons, Gi-coupled receptors (for example GABAB or α2-adrenergic receptors) inhibit adenylate cyclase, suppress neuronal activity and transmitter release, opposite to what was observed in this study. It is however possible that LC neurons might express either a variant of this receptor with a different coupling mechanism or yet another receptor that recognizes L-lactate and signals via activation of AC. Further studies are necessary to test this hypothesis.
What could be the role of L-lactate-mediated signalling to NEergic neurons? While numerous studies documented rapid L-lactate elevations evoked by various stimuli in the whole brain, very little is known about local L-lactate transients, which are highly likely to be prevalent because extracellular L-lactate is quickly taken up by both neurons and astrocytes and also drained from the CNS into the systemic circulation. It is therefore possible that local L-lactate concentrations are much more dynamic than is currently appreciated. It has also not been firmly established which mechanisms play the key role in control of glycogen breakdown by astrocytes in vivo, but NE receptors on astrocytes are ideally suited for this role48,49,50. It is therefore possible that L-lactate may act as a mediator of a positive feedback loop between NEergic varicosities and local astrocytes, whereby NE activates local astrocytes that further facilitate NE release via production of L-lactate. This mechanism could help to locally fine-tune NEergic input to numerous brain areas all innervated by the same source—the LC (Fig. 7). The physiological mechanisms that could recruit the L-lactate-mediated excitatory pathway between astrocytes and LC neurons are yet to be discovered.
All adenoviral vectors (AVV) were produced by standard homologous recombination51. To enable the visualization of NEergic neurons without concomitant opto-excitation, we expressed a monomeric red fluorescent protein52 under the control of the PRSx8 promoter, which is selectively active in NEergic neurons in the LC53.
To optically excite NEergic neurons, we expressed a fusion (kindly provided by Dr John Y. Lin, UCSD) between ChIEF, a light-sensitive cation channel with improved responses to high frequency stimulation, and a bright red fluorescent protein tdTomato, under the control of the PRSx8 promoter.
In patch clamp experiments, we used a fusion of a mutant of channelrhodopsin2, ChR2(H134R)54, with the red fluorescent protein Katushka1.3 (ref. 55). This allows excitation of astrocytes with blue light delivered by an additional laser or LED and visualization of transduced cells using green or yellow laser line of the confocal microscope. A compact transcriptionally amplified version of glial fibrillary acidic protein (GFAP) promoter was employed to enhance and target expression to astrocytes56,57. This AVV has previously been shown to elevate [Ca2+]i levels and activate astrocytic signalling and transmitter release4. Although we did not further investigate the mechanism of L-lactate production triggered by this construct, it is important to state that it is highly unlikely to be a result of membrane depolarizations characteristic of ChR2-like constructs. Rather, it is most likely a consequence of an increase in [Ca2+]i because the key regulator of glycogen breakdown, phosphorylase kinase can be directly activated by Ca2+-calmodulin, this pathway is well known and is described in various textbooks. In addition, several adenylyl cyclase isoforms that are expressed in the brain can be directly activated by a Ca2+-calmodulin58,59, for review see ref. 60. It is therefore feasible that Ca2+-calmodulin activates adenylyl-cyclase and cAMP thus formed acts by activating PKA, which phosphorylates phosphorylase kinase that in turn phosphorylates and activates glycogen phosphorylase.
To activate astrocytic G-protein-coupled receptor-mediated intracellular signalling, we employed an opsin-β2-adrenergic receptor chimera (optoβ2AR), which is derived from extracellular and transmembrane parts of rhodopsin and the intracellular domains of the β2-adrenergic receptor20. Excitation of optoβ2AR by blue light recruits the GsPCR pathway, leading to the activation of adenylate cyclase (AC) and increase in cAMP (ref. 20). The astrocyte-selective promoter sGFAP (see above) was used to express optoβ2AR in astrocytes specifically.
The use of optoβ2AR only for FCV was determined by difficulties in handling cells expressing these constructs in patch clamp experiments. While establishing whole-cell configuration, it was essential to visualize the neurons for prolonged periods of time and with fairly intensive light. Compared with ChR2, we found it difficult to avoid unsolicited activation of astrocytes when optoβ2AR were used, possibly due to the wider excitation spectrum of these receptors. This construct also has a very narrow window for functional expression, while its overexpression is detrimental to astrocytes. Although these vectors are based on the same expression system as we used previously, for this study we have performed additional studies to verify lack of ‘leak’ expression in LC neurons with sGFAP-based vectors. Fourteen slices from four separate preparations were studied using confocal microscopy. Of 438 identified DBH-positive cells (LC neurons), only one was possibly double stained. Therefore, the vector system we use does not express optogenetic actuators in LC neurons (supplementary Fig. 8). Light did not evoke any consistent effects on neuronal membrane potential or NE release in slices not transduced with astrocyte-targeted AVV or expressing an inert construct (EGFP version CASE12), Supplementary Fig. 9.
Organotypic-cultured brain slices
Experiments were performed in accordance with the UK Animals (Scientific Procedures) Act, 1986 and were approved by the local ethics committees.
Brainstem slice cultures were prepared as described previously61. In brief, Wistar rat pups of either sex (p7–9) were terminally anaesthetized with halothane and immediately decapitated. The brainstem was then removed and bathed in ice-cold dissection medium. Slices were cut at the level of the LC (200 μm thick) in cold (4 °C) sterile dissection solution using a vibrating microtome 7,000 (Campden Instruments, UK). Slices were then plated onto organotypic culture inserts (Millicell-CM, illipore) and supplied with 1 ml per /well plating medium containing the appropriate AVV, diluted to a titre of 108 TU ml–1. Slices were kept at the interface between the feeding medium (pH 7.4) and humidified atmosphere (5% CO2, 37 °C). After 3 days, the plating medium was exchanged for supplemented Neurobasal medium (Gibco, UK), which was subsequently changed twice a week. Slice cultures were allowed to settle for 7–10 days before being used for experimentation to allow AVV-mediated expression to be fully established.
Imaging of astrocytes
Primary cultures of Wistar rat pups (p2) cerebral astrocytes (adapted from62) transduced with AVV.sGFAP.optoβ2AR, seeded onto coverslips, were loaded with either Rhod-2AM (30 μM; Invitrogen, UK) or SNARF-5AM (30 μM; Invitrogen, UK) 1 h before visualization. Rhod-2AM was used as a Ca2+ indicator to avoid spectral interference with EGFP. The pH indicator SNARF-5 responds to acidification with a shift in its emission towards shorter wavelengths. Light was collected from two channels set to 550–580 nm (channel 1) and 620–700 nm (channel 2). Ratio of channel 1: channel 2 is indicative of a pH change.
Imaging experiments were carried out at 34 °C under continuous superfusion (150 ml h–1) with pH 7.4 HBS buffer in a tissue chamber mounted on a Leica-SP confocal microscope. Astrocytes were imaged in time-lapse mode (0.5 Hz) using the 543 nm laser line to excite Rhod-2 and SNARF-5. To activate optoβ2AR- or ChR2-transduced astrocytes, a 470 nm light-emitting diode-illumination system (Rapp Optoelectronic) coupled to the microscope via the epifluorescence port was employed. Changes of [Ca2+]i in individual cells were assessed by changes in relative fluorescence intensity (F/F0).
Ca2+ imaging and patch clamp of LC neurons
A cultured slice containing LC was transferred to a recording chamber mounted on an upright SP-2 confocal microscope (Leica, Germany) and continuously superfused with HEPES-buffered solution (HBS; in mM: NaCl 137, KCl 5.4, Na2HPO4 0.25, KH2PO4 0.44, CaCl2 1.3, MgSO4 1.0, NaHCO3 4.2, HEPES 10, Glucose 5.5; pH 7.4; 34±1 °C). Current-clamp whole-cell recordings were performed at a 10 kHz sampling rate using an AxoClamp 2B amplifier (Molecular Devices), a 1401 interface and Spike 2 software (both from CED, Cambridge, UK). Recording pipettes were pulled with a vertical puller (Narishige PC-10) to 3–5 mΩ resistance. The pipette solution consisted of (in mM): potassium gluconate 130, HEPES 10, EGTA 11, NaCl 4, MgCl2 2, CaCl2 1, ATP 2, GTP 1 and glucose 5. For intracellular L-lactate application, 2 mM L-lactate (pH 7.4) was introduced to the cell by a recording pipette with slightly higher impedance (8–9 mΩ) to slow down L-lactate diffusion and aid visualization of possible time dependent effects of intracellular L-lactate. In these experiments a red-coloured dye was added to the pipette (usually SNARF-5) to confirm successful dialysis of the patched neuron. For Ca2+ imaging, cells were loaded with the Ca2+ indicator Rhod-2 by recording pipette. The intracellular solution used in these experiments contained the following (in mM): potassium gluconate 130, HEPES 10, EGTA 5.5, NaCl 4, MgCl2 2, CaCl2 1, ATP 2, GTP 0.5, glucose 5 and Rhod-2 0.5. Changes in [Ca2+]i were assessed by relative fluorescence intensity (F/F0). Rhod-2 was excited using 568 nm laser line, and Rhod-2-emitted fluorescence was sampled at 580–640 nm. For further details see ref. 26. [Ca2+]i responses in LC astrocytes were visualized using a genetically encoded Ca2+ indicator Case12 expressed via an AVV with enhanced GFAP promoter. To boost the expression of the transgenes, the construct employs coordinated co-expression of a chimeric transcriptional activator NFκB-GAL4 (ref. 4).
FCV of extracellular NE
Changes in NE tissue concentrations were measured by FCV using a Millar voltammeter (PD Systems International, UK) and carbon fiber electrodes (CFE; CF10-100 obtained from World Precision Instruments, USA, or produced in house with comparable sensitivity). A symmetric, triangular wave with a range of −0.7 V to 1.3 V (5 ms; 8 Hz) was applied through the CFE to oxidize (at around +0.65 V to +1.0V) and reduce (−0.4 V to −0.6 V) NE (Fig. 5a). Slice cultures containing the LC and transduced with selected AVVs (AVV.sGFAP.optoβ2AR, AVV.PRSx8.RFP, AVV.sPRSx8.ChIEF-tdTomato) were immobilized in the recording chamber by a mesh and continuously superfused with HBS (pH 7.4, 34 °C).
The CFE was initially placed in a non-transduced area of the slice and allowed to cycle for 1 h to stabilize the baseline before recording, after which it was transferred to the LC region. Optogenetic stimulation was applied to the LC through an optical fiber (0.7 mm Ø) positioned 10–12 mm above the slice and connected to a PhoxX 445 nm laser (Omicron, Germany).
Before recording each epoch, the background electrochemical signal was subtracted using the ‘refresh’ function of the voltammeter. The resulting Faradaic signal data were acquired and analysed through a Micro1401II interface using Spike2 software (both from CED, Cambridge, UK) with scripts written in house. The NE oxidation peak (between +0.65 V and +1.0 V on the ascending scan) was plotted against time and the integrated NE oxidation in response to L-lactate or light stimulation was determined as V × s. CFEs were retracted from the tissue at the end of experiments and calibrated against NE (0.5 μM) to allow calculation of total release as μM × s. Independently of the electrode sensitivity, we can expect variability in the number of local release sites around any recording position, thus resulting in variation of measured NE volume transmission between recording sites or slices. Therefore data sets including the relevant and comparable control responses were pooled for evaluation of effects.
In vivo experiments
Eleven male Sprague–Dawley rats (300–340 g, 2.5–3 months of age) were anesthetized with urethane (1.6 g kg−1, I.P.). Adequate anaesthesia was ensured by maintaining stable levels of arterial blood pressure and heart rate. The femoral artery and vein were cannulated for measurement of arterial blood pressure and administration of anesthetic, respectively. The trachea was cannulated, and the animal was ventilated with a mixture of 50% oxygen and 50% nitrogen using a positive pressure ventilator (Harvard rodent ventilator, model 683) with a tidal volume of ~2 ml and a ventilator frequency similar to spontaneous frequency (~60 strokes min−1). The body temperature was maintained with a servo-controlled heating pad at 37.0±0.2 °C.
The animal was placed in a stereotaxic frame, and a small hole was drilled in the occipital bone overlying the left LC (AP −9.8 mm; ML −1.2 mm from bregma). For EEG recordings, two small holes were drilled on the left side of the skull above the somatosensory cortex. Stainless steel electrodes were placed in the contact with the cortical surface and secured in place with dental cement.
A three-barrelled glass micropipette (tip size 20–25 μm) was placed in the LC (9.7 mm caudal, 1.15 mm lateral from bregma and 8–8.5 mm ventral from the surface of the skull). The barrels of the micropipette contained L-glutamate (500 mM, pH 7.4), L-lactate (500 mM, pH 7.4) and saline containing 5% of fluorescent beads (Invitrogen). Drugs microinjected from pipettes in small volumes are subject to very rapid dilution and therefore activate a much larger area than the actual volume of injection. In addition, metabolites such as glutamate of L-lactate are taken up by the cells and also eliminated from the tissue into the bloodstream. On the basis of the effective concentrations of L-lactate in vitro established in this work, L-lactate could be applied at concentrations much higher than those of L-glutamate because L-glutamate receptors have high affinity, while the putative L-lactate receptor must have low affinity. Nevertheless we decided not to increase it further to avoid possible complications due to an osmotic effect. Microinjections were made using pressure over a period of 5–10 s and were monitored by observing the fluid level using a dissecting microscope with a calibrated micrometer disk. First, a unilateral microinjection of L-glutamate (40 nl) was made to document the effect of LC activation on cardiovascular variables and EEG. After a recovery period of 30–40 min, L-lactate was microinjected (40 nl) into the same LC site. The sites of microinjections were marked by injection of fluorescent beads, identified Post hoc histologically and mapped using a stereotaxic atlas63. The EEG signal was amplified via a differential amplifier (Digitimer, USA) without additional filtering.
Recordings were processed using a Power1401 interface and analyzed with Spike2 software (CED). Measurements of mean arterial blood pressure and heart rate were taken before and at the peak of the evoked responses and were compared using Student’s paired two-tailed t-test.
The power spectrum of the EEG signal was analyzed using Spike2 software using a custom-written script. 50 (±2) Hz band was excluded to avoid skewing by potential AC interference. L-lactate- and L-glutamate-induced changes in <4 Hz (delta), 4–8 Hz (theta), 8–13 Hz (alpha), 8–30 Hz (beta) and >30 (gamma) power bands were determined and compared within individual experiments.
Post hoc histology
Fixed brains were sectioned and immunostained for dopamine-β-hydroxylase, an established marker for NE neurons. Monoclonal primary antibody was used (MAB308, Millipore, 1:1,000) followed by a goat anti mouse-Alexa 488 (Invitrogen, 1:500).
The following drugs were obtained from Tocris: MRS 2179, CNQX, APV, indomethacin, tetrodotoxin, SQ22536, U73122. All other chemicals were from Sigma.
Pooled data were expressed as average ±s.e.m. Groups were compared using Student’s t-test, paired or unpaired as indicated. Microsoft Excel was used for data processing. GraphPad Prizm was used to calculate EC50 values for concentration-response curves.
How to cite this article: Tang, F. et al. Lactate-mediated glia-neuronal signalling in the mammalian brain. Nat. Commun. 5:3284 doi: 10.1038/ncomms4284 (2014).
Wang, F. et al. Astrocytes modulate neural network activity by Ca(2)+-dependent uptake of extracellular K+. Sci. Signal. 5, ra26 (2012).
Henneberger, C., Papouin, T., Oliet, S. H. & Rusakov, D. A. Long-term potentiation depends on release of D-serine from astrocytes. Nature 463, 232–236 (2010).
Gordon, G. R. et al. Astrocyte-mediated distributed plasticity at hypothalamic glutamate synapses. Neuron 64, 391–403 (2009).
Gourine, A. V. et al. Astrocytes control breathing through pH-dependent release of ATP. Science 329, 571–575 (2010).
Koizumi, S., Fujishita, K., Tsuda, M., Shigemoto-Mogami, Y. & Inoue, K. Dynamic inhibition of excitatory synaptic transmission by astrocyte-derived ATP in hippocampal cultures. Proc. Natl Acad. Sci. USA 100, 11023–11028 (2003).
Bowser, D. N. & Khakh, B. S. ATP excites interneurons and astrocytes to increase synaptic inhibition in neuronal networks. J. Neurosci. 24, 8606–8620 (2004).
Parpura, V. & Haydon, P. G. Physiological astrocytic calcium levels stimulate glutamate release to modulate adjacent neurons. Proc. Natl Acad. Sci. USA 97, 8629–8634 (2000).
Panatier, A. et al. Glia-derived D-serine controls NMDA receptor activity and synaptic memory. Cell 125, 775–784 (2006).
Bouzier-Sore, A. K., Voisin, P., Canioni, P., Magistretti, P. J. & Pellerin, L. Lactate is a preferential oxidative energy substrate over glucose for neurons in culture. J. Cereb. Blood Flow Metab. 23, 1298–1306 (2003).
Pellerin, L. et al. Evidence supporting the existence of an activity-dependent astrocyte-neuron lactate shuttle. Dev. Neurosci. 20, 291–299 (1998).
Pellerin, L. & Magistretti, P. J. Glutamate uptake into astrocytes stimulates aerobic glycolysis: a mechanism coupling neuronal activity to glucose utilization. Proc. Natl. Acad. Sci. USA 91, 10625–10629 (1994).
Dienel, G. A. Brain lactate metabolism: the discoveries and the controversies. J. Cereb. Blood Flow Metab. 32, 1107–1138 (2012).
Barros, L. F. Metabolic signaling by lactate in the brain. Trends Neurosci. 36, 396–404 (2013).
Suzuki, A. et al. Astrocyte-neuron lactate transport is required for long-term memory formation. Cell 144, 810–823 (2011).
Gibbs, M. E. & Hertz, L. Inhibition of astrocytic energy metabolism by D-lactate exposure impairs memory. Neurochem. Int. 52, 1012–1018 (2008).
Hall, C. N., Klein-Flugge, M. C., Howarth, C. & Attwell, D. Oxidative phosphorylation, not glycolysis, powers presynaptic and postsynaptic mechanisms underlying brain information processing. J. Neurosci. 32, 8940–8951 (2012).
Stone, E. A. & Ariano, M. A. Are glial cells targets of the central noradrenergic system? A review of the evidence. Brain Res. Rev. 14, 297–309 (1989).
Hertz, L., Chen, Y., Gibbs, M. E., Zang, P. & Peng, L. Astrocytic adrenoceptors: a major drug target in neurological and psychiatric disorders? Curr. Drug Targets. CNS. Neurol. Disord. 3, 239–267 (2004).
Bekar, L. K., He, W. & Nedergaard, M. Locus coeruleus alpha-adrenergic-mediated activation of cortical astrocytes in vivo. Cereb. Cortex 18, 2789–2795 (2008).
Airan, R. D., Thompson, K. R., Fenno, L. E., Bernstein, H. & Deisseroth, K. Temporally precise in vivo control of intracellular signalling. Nature 458, 1025–1029 (2009).
Chiu, T. H., Chen, M. J., Yang, Y. R., Yang, J. J. & Tang, F. I. Action of dexmedetomidine on rat locus coeruleus neurones: intracellular recording in vitro. Eur. J. Pharmacol. 285, 261–268 (1995).
Hagan, J. J. et al. Orexin A activates locus coeruleus cell firing and increases arousal in the rat. Proc. Natl Acad. Sci. USA 96, 10911–10916 (1999).
Walls, A. B. et al. Characterization of 1,4-dideoxy-1,4-imino-d-arabinitol (DAB) as an inhibitor of brain glycogen shunt activity. J. Neurochem. 105, 1462–1470 (2008).
Choi, H. B. et al. Metabolic communication between astrocytes and neurons via bicarbonate-responsive soluble adenylyl cyclase. Neuron 75, 1094–1104 (2012).
Halestrap, A. P. & Price, N. T. The proton-linked monocarboxylate transporter (MCT) family: structure, function and regulation. Biochem. J. 343, (Pt 2): 281–299 (1999).
Wang, S., Teschemacher, A. G., Paton, J. F. & Kasparov, S. Mechanism of nitric oxide action on inhibitory GABAergic signaling within the nucleus tractus solitarii. FASEB J. 20, 1537–1539 (2006).
Chan, B. S., Endo, S., Kanai, N. & Schuster, V. L. Identification of lactate as a driving force for prostanoid transport by prostaglandin transporter PGT. Am. J. Physiol. Renal Physiol. 282, F1097–F1102 (2002).
Gordon, G. R., Choi, H. B., Rungta, R. L., Ellis-Davies, G. C. & MacVicar, B. A. Brain metabolism dictates the polarity of astrocyte control over arterioles. Nature 456, 745–749 (2008).
Lin, J. Y., Lin, M. Z., Steinbach, P. & Tsien, R. Y. Characterization of engineered channelrhodopsin variants with improved properties and kinetics. Biophys. J. 96, 1803–1814 (2009).
Mastitskaya, S. et al. Cardioprotection evoked by remote ischaemic preconditioning is critically dependent on the activity of vagal pre-ganglionic neurones. Cardiovasc. Res. 95, 487–494 (2012).
Wyss, M. T., Jolivet, R., Buck, A., Magistretti, P. J. & Weber, B. In vivo evidence for lactate as a neuronal energy source. J. Neurosci. 31, 7477–7485 (2011).
Mukhtarov, M., Ivanov, A., Zilberter, Y. & Bregestovski, P. Inhibition of spontaneous network activity in neonatal hippocampal slices by energy substrates is not correlated with intracellular acidification. J. Neurochem. 116, 316–321 (2011).
Nedergaard, M. Intracellular Ca2+ transients evoked by lactic acid in cultured mammalian neurons. Am. J. Physiol. 268, R506–R513 (1995).
Song, Z. & Routh, V. H. Differential effects of glucose and lactate on glucosensing neurons in the ventromedial hypothalamic nucleus. Diabetes 54, 15–22 (2005).
Parsons, M. P. & Hirasawa, M. ATP-sensitive potassium channel-mediated lactate effect on orexin neurons: implications for brain energetics during arousal. J. Neurosci. 30, 8061–8070 (2010).
Lin, R. Y., Vera, J. C., Chaganti, R. S. & Golde, D. W. Human monocarboxylate transporter 2 (MCT2) is a high affinity pyruvate transporter. J. Biol. Chem. 273, 28959–28965 (1998).
Manning Fox, J. E., Meredith, D. & Halestrap, A. P. Characterisation of human monocarboxylate transporter 4 substantiates its role in lactic acid efflux from skeletal muscle. J. Physiol. 529, (Pt 2): 285–293 (2000).
Nedergaard, M. & Goldman, S. A. Carrier-mediated transport of lactic acid in cultured neurons and astrocytes. Am. J. Physiol. 265, R282–R289 (1993).
Demestre, M., Boutelle, M. & Fillenz, M. Stimulated release of lactate in freely moving rats is dependent on the uptake of glutamate. J. Physiol. 499, (Pt 3): 825–832 (1997).
Dienel, G. A., Ball, K. K. & Cruz, N. F. A glycogen phosphorylase inhibitor selectively enhances local rates of glucose utilization in brain during sensory stimulation of conscious rats: implications for glycogen turnover. J. Neurochem. 102, 466–478 (2007).
Chiti, Z. & Teschemacher, A. G. Exocytosis of norepinephrine at axon varicosities and neuronal cell bodies in the rat brain. FASEB J. 21, 2540–2550 (2007).
Teschemacher, A. G. & Seward, E. P. Bidirectional modulation of exocytosis by angiotensin II involves multiple G-protein-regulated transduction pathways in chromaffin cells. J. Neurosci. 20, 4776–4785 (2000).
Kaneko, M. & Takahashi, T. Presynaptic mechanism underlying cAMP-dependent synaptic potentiation. J. Neurosci. 24, 5202–5208 (2004).
Cai, T. Q. et al. Role of GPR81 in lactate-mediated reduction of adipose lipolysis. Biochem. Biophys. Res. Commun. 377, 987–991 (2008).
Ge, H. et al. Elucidation of signaling and functional activities of an orphan GPCR, GPR81. J. Lipid Res. 49, 797–803 (2008).
Liu, C. et al. Lactate inhibits lipolysis in fat cells through activation of an orphan G-protein-coupled receptor, GPR81. J. Biol. Chem. 284, 2811–2822 (2009).
Kuei, C. et al. Study of GPR81, the lactate receptor, from distant species identifies residues and motifs critical for GPR81 functions. Mol. Pharmacol. 80, 848–858 (2011).
Dienel, G. A. & Hertz, L. Glucose and lactate metabolism during brain activation. J. Neurosci. Res. 66, 824–838 (2001).
Magistretti, P. J., Sorg, O., Yu, N., Martin, J. L. & Pellerin, L. Neurotransmitters regulate energy metabolism in astrocytes: implications for the metabolic trafficking between neural cells. Dev. Neurosci. 15, 306–312 (1993).
Fillenz, M., Lowry, J. P., Boutelle, M. G. & Fray, A. E. The role of astrocytes and noradrenaline in neuronal glucose metabolism. Acta Physiologica Scandinavica 167, 275–284 (1999).
Duale, H., Kasparov, S., Paton, J. F. R. & Teschemacher, A. G. Differences in transductional tropism of adenoviral and lentiviral vectors in the rat brainstem. Exp. Physiol. 90, 71–78 (2005).
Campbell, R. E. et al. A monomeric red fluorescent protein. Proc. Natl Acad. Sci. USA 99, 7877–7882 (2002).
Hwang, D. Y., Carlezon, W. A. Jr, Isacson, O. & Kim, K. S. A high-efficiency synthetic promoter that drives transgene expression selectively in noradrenergic neurons. Hum. Gene Ther. 12, 1731–1740 (2001).
Nagel, G. et al. Light activation of channelrhodopsin-2 in excitable cells of Caenorhabditis elegans triggers rapid behavioral responses. Curr. Biol. 15, 2279–2284 (2005).
Shcherbo, D. et al. Far-red fluorescent tags for protein imaging in living tissues. Biochem. J. 418, 567–574 (2009).
Liu, B. H., Paton, J. F. R. & Kasparov, S. Viral vectors based on bidirectional cell-specific mammalian promoters and transcriptional amplification strategy for use in vitro and in vivo. BMC Biotechnol. 8, 49 (2008).
Figueiredo, M. et al. Optogenetic experimentation on astrocytes. Exp. Physiol. 96, 40–50 (2011).
Feinstein, P. G. et al. Molecular cloning and characterization of a Ca2+/calmodulin-insensitive adenylyl cyclase from rat brain. Proc. Natl Acad. Sci. USA 88, 10173–10177 (1991).
Masada, N., Schaks, S., Jackson, S. E., Sinz, A. & Cooper, D. M. Distinct mechanisms of calmodulin binding and regulation of adenylyl cyclases 1 and 8. Biochemistry 51, 7917–7929 (2012).
Iwatsubo, K., Tsunematsu, T. & Ishikawa, Y. Isoform-specific regulation of adenylyl cyclase: a potential target in future pharmacotherapy. Expert. Opin. Ther. Targets 7, 441–451 (2003).
Teschemacher, A. G., Paton, J. F. R. & Kasparov, S. Imaging living central neurones using viral gene transfer. Adv. Drug Delivery Rev. 57, 79–93 (2005).
Marriott, D. R., Hirst, W. D. & Ljungberg, M. C. Astrocytes. inNeural Cell Culture—A Oractical Approach (eds Cohen J., Wilkin G. P. 85–96Oxford University Press (1995).
Paxinos, G. & Watson, C. The Rat Brain in Stereotaxic Coordinates Academic Press Ltd. (1986).
We are grateful to Dr B.H. Liu, Ms L. Arberry and M. Figueiredo who provided help with generation of various viral vector constructs used in this study, and to Drs K.A. Jennings and S.J. Cragg, Oxford, for expert advice on FCV. The ChIEF-tdTomato construct was kindly provided by Dr J.Y. Lin (UCSD). Other optogenetic constructs were kindly provided by Professor K. Deisseroth (Stanford University). This study was supported by the British Heart Foundation (PG09/064), MRC (MR/J013110/1) and The Wellcome Trust (A.V.G. is a Wellcome Trust Senior Research Fellow).
The authors declare no competing financial interests.
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Tang, F., Lane, S., Korsak, A. et al. Lactate-mediated glia-neuronal signalling in the mammalian brain. Nat Commun 5, 3284 (2014). https://doi.org/10.1038/ncomms4284
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