Search tips
Search criteria 


Logo of wtpaEurope PMCEurope PMC Funders GroupSubmit a Manuscript
J Neurosci. Author manuscript; available in PMC 2009 September 3.
Published in final edited form as:
PMCID: PMC2737175



Acid-sensitive K+-channels of the tandem P-domain K+-channel family (TASK-1 & -3) have been implicated in peripheral and central respiratory chemosensitivity, however, because of the lack of decisive pharmacological agents, the final proof of the TASK channel's role in the chemosensory control of breathing has been missing. In the mouse TASK-1 and TASK-3 channels are dispensable for central respiratory chemosensitivity (Mulkey et al., 2007). Here we have used knockout animals to determine whether TASK-1 and TASK-3 channels play a role in the carotid body function and chemosensory control of breathing exerted by the carotid body chemoreceptors. Ventilatory responses to hypoxia (10% O2 in inspired air) and moderate normoxic hypercapnia (3-6% CO2 in inspired air) were significantly reduced in TASK-1 knockout mice. In contrast TASK-3 deficient mice showed responses to both stimuli that were similar to those developed by their wild-type counterparts. TASK-1 channel deficiency resulted in a marked reduction of the hypoxia- (by 49%) and CO2 (by 68%) -evoked increases in the carotid sinus nerve chemoafferent discharge recorded in the in vitro superfused carotid body/carotid sinus nerve preparations. Deficiency in both TASK-1 and TASK-3 channels increased baseline chemoafferent activity but did not cause a further reduction of the carotid body chemosensory responses. These observations provide direct evidence that TASK-1 channels contribute significantly to the increases in the carotid body chemoafferent discharge in response to a decrease in arterial PO2 or an increase in PCO2/[H+]. TASK-1 channels therefore play a key role in the control of ventilation by peripheral chemoreceptors.

Keywords: Carotid body, chemosensitivity, hypercapnia, hypoxia, respiration, TASK


The basic rhythm of breathing is generated within the pre-Bötzinger complex of the medulla oblongata and then subsequently shaped, modified and transmitted to the bulbospinal pre-motor neurons which relay the resulting respiratory pattern to the spinal motor neurons controlling respiratory muscles (Feldman et al., 2003;Feldman and Del Negro, 2006). The brainstem respiratory network continuously receives chemoafferent information about the arterial levels of PO2, PCO2 and pH and adjusts respiratory motor output, ensuring appropriate ventilation of the lungs in various environmental and physiological conditions.

In mammals, respiratory chemoafferent inputs originate primarily from the receptors in the carotid bodies and from the central chemoreceptors in the brainstem (Nattie, 1999;Feldman et al., 2003;Lahiri et al., 2006;Kumar, 2007). Type I (glomus) cells of the carotid body are the principal peripheral chemosensitive elements which rapidly detect alterations in arterial levels of PO2, PCO2 and pH, transmit this information to the chemoafferent fibers of the carotid sinus nerve, which in turn relays to the brainstem respiratory centers to evoke adaptive changes in ventilation. PCO2 and pH are also monitored by the chemoreceptors localized within the brainstem – primarily at, or in close proximity to, the ventral surface of the medulla oblongata (Loeschcke, 1982;Mulkey et al., 2004), and possibly in several other distinct brainstem regions (Nattie, 1999;Putnam et al., 2004).

Acid-sensitive K+-channels of the tandem P-domain K+-channel family (TASKs) have been proposed to contribute significantly to various aspects of the chemosensory control of breathing. TASK currents are inhibited by external acidic pH, activated by alkali (Duprat et al., 1997;Rajan et al., 2000;Kim et al., 2000), and reduced by low O2 (Lewis et al., 2001). TASK-1 (KCNK3) homodimers go from open to shut within 0.5 pH units around pH 7.4 (Duprat et al., 1997) whereas TASK-3 (KCNK9) channels shut under more acid conditions (Rajan et al., 2000). TASK-1 and TASK-3 can form homo- or heterodimeric channels (Czirjak and Enyedi, 2002;Berg et al., 2004).

Type I cells of the carotid body express a prominent background K+ conductance that displays some TASK-like properties (including weak outward rectification, inhibition by low pH and activation by halothane (Buckler et al., 2000)) and is inhibited by hypoxia (Buckler, 2007). In addition, the TASK genes are expressed in all central CO2 chemosensitive regions (Talley et al., 2001), including areas of the ventrolateral medulla (Washburn et al., 2003), raphe nuclei (Washburn et al., 2002), and locus coeruleus (Bayliss et al., 2001). However, in mice TASK-1 and TASK-3 channels appear to be dispensable for central respiratory chemosensitivity (Mulkey et al., 2007).

Primarily due to the lack of specific inhibitors for these channels it is still unknown if and how TASK-1 and TASK-3 channels contribute to the carotid body function and the control of ventilation exerted by these peripheral chemoreceptors. Here using knockout mice we directly confirm that TASK-1 channel does not indeed contribute to the central respiratory chemosensitivity but appears to be essential for the carotid body CO2/pH sensitivity and also contributes significantly to the mechanism of oxygen sensing in the carotid body.



The TASK-1−/− and TASK-3−/− mice used in this study have been described in detail previously (Aller et al., 2005;Brickley et al., 2007). In both lines, the first coding exon of the respective gene is destroyed and the mutant allele not transcribed. TASK-1−/− and TASK-3−/− mice were largely on the C57Bl/6 background. We used adult (3-4 months) TASK-1−/−, TASK-3−/− mice and their respective wild-type counterparts. Double knockout mice (TASK-1−/−:TASK-3−/−) were produced by inter-breeding the individual knockout strains. Genotypes were confirmed by PCR using genomic DNA from ear biopsies as template. Double knockout mice appeared overtly healthy, and could be bred with each other. All experiments were carried out in accordance with the UK Animals (Scientific Procedures) Act, 1986.

Whole body plethysmography

Respiratory rate (fR, breaths min−1) and tidal volume (VT, ml kg−1) in conscious freely moving mice were measured by whole body plethysmography as described in detail previously (Onodera et al., 1997;Rong et al., 2003). All experiments were carried out at room temperature (22-24°C). In brief, the mouse was placed in a Plexiglas recording chamber (~400 ml) which was flushed continuously with a mixture of 79% nitrogen and 21% oxygen (unless otherwise required by the protocol) at a rate of ~1 L min−1. Concentrations of O2 and CO2 in the chamber were monitored on-line using a fast-response O2/CO2 monitor (Morgan Medical, UK). The animals were allowed at least 30 min to acclimatize to the chamber environment at normoxia/normocapnia (21% O2, 79% N2 and <0.3% CO2) before measurements of baseline ventilation were taken. Hypoxia was induced by lowering the O2 concentration in the inspired air down to a level of 10% for 5 min. In separate experiments, normoxic hypercapnia was induced by titrating CO2 into the respiratory mixture up to a level of 3, 6 or 10% (lowering N2 accordingly) for 5 min at each CO2 level. The pressure signal was amplified, filtered, recorded and analyzed offline using Spike 2 software (Cambridge Electronic Design, UK). The measurements of the fR and VT were taken during the last 2 min before exposure to the stimulus and during the 2 minute period at the end of each stimulus, when breathing stabilized. Hypoxia- or hypercapnia-induced changes in the fR, VT and minute ventilation (VE; fR × VT; ml min−1 kg−1) were averaged and expressed as means ± standard error (S.E.).

In situ brainstem–spinal cord preparation

A separate experiment was conducted using in situ brainstem-spinal cord preparations described in detail previously (Paton, 1996). In brief, TASK+/+ and TASK-1−/− mice were given heparin (500 units, i.p.), anesthetized deeply with halothane until loss of paw withdrawal reflex, bisected under the diaphragm, immersed in cold carbogenated Ringer solution, and decerebrated precollicularly. Preparations were then transferred to a recording chamber and a double lumen cannula was placed into the descending aorta for retrograde perfusion with carbogenated (saturated with 95% O2/5% CO2) solution containing (in mM) 124 NaCl, 26 NaHCO3, 3 KCl, 2 CaCl2, 1.25 MgSO4, 1.25 KH2PO4, and 10 dextrose (PCO2 40 mmHg, pH 7.4, 32°C). Ficoll 70 (1.25%) was added as an oncotic agent and vecuronium bromide (4 μg/ml) was added to block neuromuscular transmission. Aortic perfusion pressure was monitored via the second lumen of the cannula. Both vagi and carotid sinus nerves were cut to eliminate inputs from the peripheral chemoreceptors. Activity of the phrenic nerve was recorded using a suction electrode. Nerve activity was amplified, filtered (0.1-3 kHz), rectified and integrated (50-ms time constant) relayed to a computer and recorded using a 1401 interface and Spike 2 software.

In a preliminary study using rats we found relatively weak respiratory responses of the preparations with denervated peripheral chemoreceptors when extra CO2 was applied (saturating the perfusate with 90%O2/10%CO2). Therefore, in this study to assess the central respiratory chemosensitivity the amount of CO2 bubbled through the solution was lowered to 3% (resulting in a solution's PCO2 of 26 mmHg and pH of 7.52) and then increased to 8% (PCO2 60 mmHg, pH 7.24) leading to a significant and reproducible increases in the amplitude of the phrenic nerve discharge (Fig. 1C). This protocol was used in the current study.

Figure 1
TASK-1 channel is essential for the development of normal ventilatory responses to hypoxia and CO2 in mice

In vitro sinus nerve recording

To assess carotid body function, superfused preparations of the carotid body/carotid sinus nerve were used (Rong et al., 2003). Mice were terminally anaesthetized with halothane (6% in air mixture) and were decapitated at the lower cervical level. The head was placed in a chamber with circulating ice cold Krebs solution saturated with 95% O2/5% CO2. The region of the carotid bifurcation containing the carotid body and the attached sinus nerve was dissected under a microscope and was placed into a recording chamber (1 ml). The preparation was superfused with carbogenated (saturated with 95% O2/5% CO2) solution containing (in mM) 124 NaCl, 3 KCl, 2 CaCl2, 26 NaHCO3, 1.25 NaH2PO4, 1 Mg(SO4)2, 10 D-glucose (PCO2 40 mmHg, pH 7.4). Perfusion rate was 6 ml min−1 and the temperature in the chamber was kept constant at 37°C. The sinus nerve was desheathed and recordings were made using a suction electrode. The chemoafferent activity was amplified, filtered (0.2-3 kHz), relayed to a computer and recorded using 1401 interface and Spike 2 software.

Hypoxia was induced for 3 min by perfusing the chamber with the above solution in which O2 had been replaced by bubbling it with 95% N2/5% CO2. Changes in the PO2 of the perfusate were monitored on-line using an oxygen meter (model ISO2; World Precision Instruments, USA). The analogue of hypercapnia (respiratory acidosis) was induced for 5 min by perfusing the chamber with solution in which extra CO2 had been added to increase PCO2 from its normal value of 40 mmHg to 65 mmHg which is accompanied by a reduction in pH from 7.4 to 7.2 (PCO2 and pH values were measured using a Siemens Blood Gas Analyzer).

Data analysis

Recordings were processed using a 1401 interface and analyzed using Spike 2 software. Discharge frequency of the whole carotid sinus nerve was determined after discrimination of activity with a window discriminator (Digitimer D130 Spike Processor, Digitimer, UK). The level of background noise was determined before each experiment by placing recording electrode outside the preparation. Analysis of single chemoafferent fiber discharge was performed using the spike-sorting function of the Spike 2 program as described in detail previously (Rong et al., 2003). Changes in the whole nerve and single chemoafferent fiber activities are presented as peaks (the highest level of activity during the period of stimulation, in spikes s−1) and integral (frequency versus time, ∫ΔFF) increases in discharge. Integral increases in activity during the same time periods were determined by measuring area under the curve relative to a straight line joining the level of discharge before and after the stimulus.

All the data are reported as means ± S.E. Comparisons between experimental groups were made using Student's t test or ANOVA followed by the Tukey-Kramer's post-hoc test, as appropriate. A value of P<0.05 was considered to be significant.


Impaired ventilatory response to hypoxia in TASK-1−/− mice

The resting ventilation in normoxia/normocapnia was similar in TASK-1−/− (1.58±0.09 ml min−1 g−1, n=8) and their wild-type counterparts (1.79±0.09 ml min−1 g−1, n=7; P=0.12). When challenged with hypoxia (10% O2 in the inspired air) wild-type mice showed an increased rate (fR) and depth of breathing (VT) and therefore an increased minute ventilation (VE, Fig. 1A). This hypoxia-induced increase in ventilation was markedly reduced in TASK-1−/− animals (Fig. 1A). Thus, in the air containing 10% O2, increases in tidal volume were smaller in TASK-1−/− mice resulting in VE of 2.04±0.14 ml min−1 g−1 (n=8) whereas in the wild-type animals VE was 2.94±0.19 ml min−1 g−1 (n=7) (P<0.05). The hypoxia-induced decrease in core body temperature in TASK-1−/− mice was not significantly different from that in TASK+/+ animals (−0.7±0.1°C, n=3 vs −0.8±0.3°C, n=4; P=0.7). The resting ventilation and the ventilatory response of TASK-3−/− and TASK+/+ mice to hypoxic stimulation were similar (Fig. 2A).

Figure 2
TASK-3 channel is not required for the development of the ventilatory responses to hypoxia and CO2 in mice

Impaired ventilatory response to CO2 in TASK-1−/− mice

Mice lacking TASK-1 or TASK-3 channels were exposed to graded levels of normoxic hypercapnia, which induced profound increases in ventilation in all groups of animals (Figs. (Figs.1B1B and and2B).2B). TASK-1−/− mice displayed significantly smaller ventilatory responses to moderate levels of inspired CO2 (Fig. 1B). In an atmosphere of 3% and 6% CO2, VE in TASK-1−/− mice increased to 2.56±0.20 ml min−1 g−1 and 4.66±0.27 ml min−1 g−1 (n=7), while in the wild-type animals in the same conditions VE was elevated to 3.94±0.32 ml min−1 g−1 (P<0.05) and 5.97±0.34 ml min−1 g−1 (P<0.05) (n=7), respectively (Fig. 1B). Separate groups of TASK-1−/− (n=3) and wild-type (n=4) mice were also challenged with high level of hypercapnia (10% CO2 in the inspired air). In these conditions the difference in minute ventilation between TASK-1−/− and TASK+/+ mice was no longer observed (6.9±0.91 ml min−1 g−1 vs 6.17±0.83 ml min−1 g−1, respectively; P=0.57), although, the increase in the rate of breathing was significantly smaller in TASK-1−/− animals (345±8 vs 394±5 breaths min−1, P<0.05). Respiratory responses to increases in PCO2/[H+] of the in situ brainstem–spinal cord preparations of TASK-1−/− and TASK+/+ mice with denervated peripheral chemoreceptors were similar (Fig. 1C). No significant differences in any measures of ventilation were detected between TASK-3−/− and the wild-type control mice when concentration of CO2 in the inspired air increased to 3% or 6% (Fig. 2B).

Impaired carotid body function in TASK-1−/− mice

The results of the whole body plethysmography experiments presented above strongly suggested that carotid body function is compromised in TASK-1 deficient mice. To test this hypothesis we recorded activity of the carotid sinus nerve in in vitro superfused carotid body/carotid sinus nerve preparations taken from wild-type and TASK-1−/− mice. Hypoxia- and CO2-evoked increases in the carotid sinus nerve chemoafferent discharge were recorded and the effect of TASK-1 deficiency on these responses was determined. In preparations taken from TASK+/+ animals hypoxic stimulation evoked a dramatic increase in the carotid sinus nerve discharge – the whole nerve chemoafferent activity increased from 50±9 spikes s−1 to a peak of 414±37 spikes s−1 (n=8; Fig. 3A and 3C). In preparations taken from TASK-1−/− mice hypoxia-induced increases in the carotid sinus nerve peaked at 221±31 spikes s−1 (n=10; Fig. 3A and 3C), representing some 49% reduction in the whole-nerve response to a decrease in PO2 (P<0.05). Accordingly, the average hypoxia induced peak firing rate of single chemoafferent fibers was significantly reduced in the carotid body/sinus nerve preparations from TASK-1−/− mice (5.4±0.8, n=27 vs 14.6±1.5, n=31 in TASK+/+ mice; P<0.05; Fig. 4B).

Figure 3
Impaired carotid body function in TASK deficient mice
Figure 4
Single unit analysis of the carotid sinus nerve responses to chemosensory stimulation in TASK deficient mice

Genetic ablation of TASK-1 not only reduced the peak of the response to hypoxia, but also made it more transient. Consequently, the area under the curve of the frequency versus time plot was calculated to compare the responses (Figs. (Figs.3E3E and and4B4B).

In preparations taken from wild-type mice carotid sinus nerve chemoafferent discharge also significantly increased (peak 102±15 spikes s−1, n=8) in response to respiratory acidosis (increase in PCO2/[H+]), albeit to a lesser degree compared to that during hypoxia (Fig. 3B and 3D). Hypercapnia-evoked increase in the carotid sinus nerve discharge was considerably reduced in preparations taken from TASK-1−/− mice (peak 49±10 spikes s−1, n=10, P<0.05). This represents a 68% reduction of the response in the knockout animals (Fig. 3B and 3D). Moreover, in TASK-1−/− mice the increase of discharge in response to CO2 failed to reach significance. Similarly, the average CO2-induced peak increase in the activity of single sinus nerve chemoafferent fibers was significantly lower in preparations taken from the TASK-1−/− mice (1.2±0.2 spikes s−1, n=27 vs 3.7±0.7 spikes s−1, n=31 in TASK+/+, P<0.05, Fig. 4C).

Impaired carotid body function in TASK-1−/−:TASK-3−/− double KO mice

The results presented above demonstrated a blunted but not abolished carotid body response to hypoxia in mice deficient in TASK-1 channels. To test whether the remaining response to hypoxic stimulation might be attributable to TASK-3 channels, experiments were conducted using the carotid body/carotid sinus nerve preparations taken from TASK-1/TASK-3 double KO mice. In was found that in these animals the average basal firing rate of single chemoafferent fibers (4.1±0.7 spikes s−1, n=31, Fig. 4B and 4C) and accordingly the activity of the whole carotid sinus nerve (Fig. 3A-D) were significantly (P<0.05) higher compared to both TASK+/+ or TASK-1−/− mice (basal firing of single units 0.9±0.2 and 0.6±0.1 spikes s−1, respectively). However, the absolute increase in discharge frequency in response to hypoxia or CO2 were significantly reduced compared to TASK+/+ mice and very similar to that observed in preparations taken from TASK-1−/− mice, both at the whole nerve and single chemoafferent fiber levels (Figs. 3C-F, 4B and 4C).


Our observations provide the first direct evidence that TASK-1 channels contribute significantly to the increases in the carotid body chemoafferent discharge in response to a decrease in arterial PO2 or an increase in PCO2/[H+] and, therefore, play an important role in the control of ventilation by the peripheral chemoreceptors. Another member of the tandem P-domain K+-channel family, TASK-3, is not essential for mediating changes in breathing in response to chemosensory stimulation.

TASK-1 channels and central CO2 chemoreception

TASK channels are expressed in various central CO2 chemosensitive regions including ventrolateral medulla (Washburn et al., 2003), medullary dorsal and caudal raphe (Washburn et al., 2002) and pontine locus coeruleus (Bayliss et al., 2001) and considering their unique sensitivity to small changes in external pH, have been proposed to participate in central CO2/pH chemoreception (Mulkey et al., 2004;Putnam et al., 2004). However, Mulkey et al (2007) demonstrated recently that mouse TASK-1 and TASK-3 channels are non-essential for central respiratory chemosensitivity. Indeed, although increases in the carotid chemoafferent discharge evoked by rising levels of PCO2/[H+] were reduced in our TASK-1−/− mice, these animals still developed vigorous ventilatory responses to CO2. This is not surprising considering that the brainstem chemosensitive sites account for up to 80% of the overall CO2-evoked ventilatory response when peripheral chemoafferent input is interrupted experimentally (Heeringa et al., 1979).

Our data agree with the evidence of Mulkey et al (2007) who demonstrated, using independently generated mice, that TASK-1, TASK-3 and TASK-1/TASK-3 double knockout animals develop normal ventilatory responses to hyperoxic hypercapnia. Considering that peripheral chemoreceptors can still discharge even at high levels of PO2 we conducted experiments using in situ working brainstem–spinal cord preparations from TASK-1−/− and TASK+/+ mice in which peripheral chemoreceptors were surgically denervated. No difference was observed in CO2-induced respiratory responses between preparations taken from TASK-1−/− and TASK+/+ mice confirming conclusions of Mulkey et al (2007) that TASK-1 channel is indeed dispensable for central respiratory chemosensitivity.

In our study, mice were also challenged with normoxic hypercapnia and the differences in the ventilatory responses between TASK-1−/− and wild-type mice were only observed at moderate levels of hypercapnia (3% or 6% CO2 in inspired air) reflecting impairment of the carotid body function. It was also found that TASK-1−/− and wild-type mice mounted similar ventilatory responses to severe levels of hypercapnia (10% CO2 in the inspired air) confirming that intact central CO2 chemoreceptors can fully compensate for the loss of the peripheral chemoafferent input under these conditions. These data also indicate that TASK channel deficiency does not impair the function of the medullary respiratory rhythmogenic neurones as well as respiratory premotor and motor neurones – all of which were found previously to express TASK channels (Washburn et al., 2003) implicated in the control of motoneuronal excitability (Bayliss et al., 2003).

TASK-1 channels and chemoreception in the carotid body

Hypoxia-induced inhibition of K+-channels in type I cells, first demonstrated almost two decades ago (Lopez-Barneo et al., 1988), is believed to constitute the key event in the carotid body chemosensory transduction mechanism (for recent reviews, see (Kemp, 2006;Buckler, 2007;Kumar, 2007). Inhibition of K+-channels leads to depolarization (Buckler, 1997), Ca2+ entry through voltage-gated Ca2+ channels (Buckler and Vaughan-Jones, 1994a;Buckler and Vaughan-Jones, 1994b), and subsequent activation of the carotid sinus nerve chemoafferent fibers via release of ATP and acetylcholine (Zhang et al., 2000;Rong et al., 2003). The exact mechanisms leading to inhibition of K+-channels are unresolved (Kemp, 2006;Kumar, 2007), but rat type I cells express background K+ channels which display some TASK-like properties, showing greatest similarity to TASK-1 and TASK-3 (reviewed in Buckler, 2007).

The proof of the functional role played by these TASK channels in the carotid body chemoreception has been missing. Both TASK-1 and TASK-3 immunoreactivities have been demonstrated in the rat carotid body (Yamamoto et al., 2002;Yamamoto and Taniguchi, 2006), however, some of these antibodies still bind to knockout brain tissue (Aller et al., 2005;Brickley et al., 2007). Here using knockout mice we demonstrated that TASK-1 channel deficiency abolished the carotid sinus nerve responses to hypercapnia. However, loss of a ‘background’ potassium conductance would be expected to cause an increase in baseline activity which we did not observe. Similarly to this, Aller et al (2005) reported that the resting membrane potential of cerebellar granule cells was not reduced in TASK-1−/− mice. They demonstrated that this was due to a replacement of TASK-1 channels, or TASK-1/TASK-3 heterodimeric channels by TASK-3 channels. This could also explain our present observations. TASK-3 channels would replace the TASK-1 homodimers or TASK-1/TASK-3 heterodimers in the carotid body type I cells, thus preventing depolarizing shift of the membrane potential. Furthermore, the acid-shifted pH-sensitivity of TASK-3 homodimeric channels (for review: Duprat et al., 2007) would explain why no response was observed during hypercapnia, which was accompanied by a moderate decrease in pH from 7.4 to 7.2.

These conclusions were further supported by the results obtained using TASK-1/TASK-3 double knockout mice. These animals displayed the same reduced carotid chemoafferent response to hypoxia and hypercapnia as the TASK-1−/− mice, evident from both smaller increase in frequency for the peak response, and smaller area under the curve for the frequency versus time plot (Figs. (Figs.33 and and4).4). However, these blunted responses were developing from an increased level of baseline activity as compared to both wild type and TASK-1−/− preparations. This would be expected because in these animals both TASK-1 and TASK-3 channels are lost and the depolarizing shift of the membrane potential cannot be prevented, which is reflected in the increased baseline firing rate of the carotid sinus nerve. The pH sensitivity is similarly lost, specifically because TASK-1 is not present.

Similarly to these results, Mulkey at al (2007) noted a significant hyperventilation during hypoxia (10% O2) in TASK-1/TASK-3 double knockout mice. In their case ventilation during hypoxia in TASK-1−/−:TASK-3−/− mice was not significantly different from that in the controls, most likely reflecting this increased level of the peripheral chemoafferent activity in the double knockout mice.

In summary, TASK-1 channels (but not TASK-3 channels) indeed play an important role in the mechanisms leading to an increase in the carotid sinus nerve chemoafferent discharge during hypoxia and hypercapnia. The response to an increase in PCO2/[H+] was abolished in both TASK-1−/− and TASK-1/TASK-3 double KO carotid body preparations. Also, the hypoxia-induced responses were significantly attenuated, though not abolished by TASK-1 deficiency. This suggests the existence of either a parallel mechanism of hypoxic chemotransduction which works in synergy with the one involving TASK-1 channels, or a mechanism which can partially compensate for the loss of the latter in the knockout animals, or both. Likewise, whereas TASK-3 channels were not essential for the expression of the hypoxic ventilatory response, we cannot exclude that they still play a role in normal conditions, but TASK-1 (or other K+ channels) can fully compensate for their loss in the knockout mice.

Since hypoxia does not stimulate respiration centrally, it is unsurprising that the reduced responsiveness of the carotid bodies to hypoxia in TASK-1−/− mice resulted in a roughly similar reduction of the overall ventilatory response. In contrast, the attenuation of the CO2-evoked ventilatory response was smaller than the attenuation of the CO2-evoked increases in the carotid sinus nerve chemoafferent discharge in the TASK-1−/− animals. These data indicate that in the carotid body TASK-1 channels play an even more significant role in sensing alterations in PCO2/[H+]. Indeed, in our experimental conditions an increase in PCO2/[H+] failed to evoke significant increases in the carotid sinus nerve discharge in preparations taken from either TASK-1 or TASK-1/TASK-3 double knockout mice. TASK-1 channels are uniquely sensitive to changes in external pH within the physiological range 7.3-7.4 (Duprat et al., 1997). Since changes in external pH which follow changes in PCO2 represent the adequate and main stimuli for the carotid body chemoreceptors (see e.g. (Gray, 1968)) TASK-1 channels are ideally suited to act as the primary PCO2/[H+] chemosensors of type I cells. Other acid-sensing ion channels (Tan et al., 2007) may work in synergy with TASK-1, however, their relative contribution to PCO2/[H+] sensitivity in the carotid body appears to be insignificant.


The data obtained in the present study indicate that in the carotid body TASK-1 channels account for at least half of the increases in the chemoafferent discharge in response to hypoxia, mediate CO2/pH sensitivity and, therefore, play a key role in the control of ventilation exerted by the peripheral respiratory chemoreceptors. This function alone would be expected to maintain a high selection pressure for the TASK-1 gene. Whereas decreases in extracellular pH which follow increases in PCO2 could directly inhibit TASK-1 channels expressed by chemosensitive type I cells of the carotid body, the actual oxygen sensor as well as biochemical pathways leading from the oxygen sensor to inhibition of these channels during hypoxia have not been definitely identified. The parallel (or compensatory) mechanism(s) of oxygen sensitivity not involving TASK channels and responsible for the residual chemoafferent responses observed in the TASK-1 knockout mice also remain to be determined.


We are grateful to the Medical Research Council (ST),The Wellcome Trust (AVG) and the J Ernest Tait Estate (WW) for financial support.


  • Aller MI, Veale EL, Linden AM, Sandu C, Schwaninger M, Evans LJ, Korpi ER, Mathie A, Wisden W, Brickley SG. Modifying the subunit composition of TASK channels alters the modulation of a leak conductance in cerebellar granule neurons. J Neurosci. 2005;25:11455–11467. [PubMed]
  • Bayliss DA, Sirois JE, Talley EM. The TASK family: two-pore domain background K+ channels. Mol Interv. 2003;3:205–219. [PubMed]
  • Bayliss DA, Talley EM, Sirois JE, Lei Q. TASK-1 is a highly modulated pH-sensitive ‘leak’ K+ channel expressed in brainstem respiratory neurons. Respir Physiol. 2001;129:159–174. [PubMed]
  • Berg AP, Talley EM, Manger JP, Bayliss DA. Motoneurons express heteromeric TWIK-related acid-sensitive K+ (TASK) channels containing TASK-1 (KCNK3) and TASK-3 (KCNK9) subunits. J Neurosci. 2004;24:6693–6702. [PubMed]
  • Brickley SG, Aller MI, Sandu C, Veale EL, Alder FG, Sambi H, Mathie A, Wisden W. TASK-3 two-pore domain potassium channels enable sustained high-frequency firing in cerebellar granule neurons. J Neurosci. 2007;27:9329–9340. [PubMed]
  • Buckler KJ. A novel oxygen-sensitive potassium current in rat carotid body type I cells. J Physiol. 1997;498:649–662. [PubMed]
  • Buckler KJ. TASK-like potassium channels and oxygen sensing in the carotid body. Respir Physiol Neurobiol. 2007;157:55–64. [PubMed]
  • Buckler KJ, Vaughan-Jones RD. Effects of hypercapnia on membrane potential and intracellular calcium in rat carotid body type I cells. J Physiol. 1994a;478:157–171. [PubMed]
  • Buckler KJ, Vaughan-Jones RD. Effects of hypoxia on membrane potential and intracellular calcium in rat neonatal carotid body type I cells. J Physiol. 1994b;476:423–428. [PubMed]
  • Buckler KJ, Williams BA, Honore E. An oxygen-, acid- and anaesthetic-sensitive TASK-like background potassium channel in rat arterial chemoreceptor cells. J Physiol. 2000;525:135–142. [PubMed]
  • Czirjak G, Enyedi P. Formation of functional heterodimers between the TASK-1 and TASK-3 two-pore domain potassium channel subunits. J Biol Chem. 2002;277:5426–5432. [PubMed]
  • Duprat F, Lauritzen I, Patel A, Honore E. The TASK background K2P channels: chemo- and nutrient sensors. Trends Neurosci. 2007;30:573–580. [PubMed]
  • Duprat F, Lesage F, Fink M, Reyes R, Heurteaux C, Lazdunski M. TASK, a human background K+ channel to sense external pH variations near physiological pH. EMBO J. 1997;16:5464–5471. [PubMed]
  • Feldman JL, Del Negro CA. Looking for inspiration: new perspectives on respiratory rhythm. Nat Rev Neurosci. 2006;7:232–242. [PMC free article] [PubMed]
  • Feldman JL, Mitchell GS, Nattie EE. Breathing: rhythmicity, plasticity, chemosensitivity. Annu Rev Neurosci. 2003;26:239–266. [PMC free article] [PubMed]
  • Gray BA. Response of the perfused carotid body to changes in pH and PCO2. Respir Physiol. 1968;4:229–245. [PubMed]
  • Heeringa J, Berkenbosch A, Olievier CN. Relative contribution of central and peripheral chemoreceptors to the ventilatory response to CO2 during hyperoxia. Respir Physiol. 1979;37:365–379. [PubMed]
  • Kemp PJ. Detecting acute changes in oxygen: will the real sensor please stand up? Exp Physiol. 2006;91:829–834. [PubMed]
  • Kim Y, Bang H, Kim D. TASK-3, a new member of the tandem pore K+ channel family. J Biol Chem. 2000;275:9340–9347. [PubMed]
  • Kumar P. Sensing hypoxia in the carotid body: from stimulus to response. Essays Biochem. 2007;43:43–60. [PubMed]
  • Lahiri S, Roy A, Baby SM, Hoshi T, Semenza GL, Prabhakar NR. Oxygen sensing in the body. Prog Biophys Mol Biol. 2006;91:249–286. [PubMed]
  • Lewis A, Hartness ME, Chapman CG, Fearon IM, Meadows HJ, Peers C, Kemp PJ. Recombinant hTASK1 is an O2-sensitive K+ channel. Biochem Biophys Res Commun. 2001;285:1290–1294. [PubMed]
  • Loeschcke HH. Central chemosensitivity and the reaction theory. J Physiol. 1982;332:1–24. [PubMed]
  • Lopez-Barneo J, Lopez-Lopez JR, Urena J, Gonzalez C. Chemotransduction in the carotid body: K+ current modulated by PO2 in type I chemoreceptor cells. Science. 1988;241:580–582. [PubMed]
  • Mulkey DK, Stornetta RL, Weston MC, Simmons JR, Parker A, Bayliss DA, Guyenet PG. Respiratory control by ventral surface chemoreceptor neurons in rats. Nat Neurosci. 2004;7:1360–1369. [PubMed]
  • Mulkey DK, Talley EM, Stornetta RL, Siegel AR, West GH, Chen X, Sen N, Mistry AM, Guyenet PG, Bayliss DA. TASK channels determine ph sensitivity in select respiratory neurons but do not contribute to central respiratory chemosensitivity. J Neurosci. 2007;27:14049–14058. [PubMed]
  • Nattie E. CO2, brainstem chemoreceptors and breathing. Prog Neurobiol. 1999;59:299–331. [PubMed]
  • Onodera M, Kuwaki T, Kumada M, Masuda Y. Determination of ventilatory volume in mice by whole body plethysmography. Jpn J Physiol. 1997;47:317–326. [PubMed]
  • Paton JFR. A working heart-brainstem preparation of the mouse. J Neurosci Methods. 1996;65:63–68. [PubMed]
  • Putnam RW, Filosa JA, Ritucci NA. Cellular mechanisms involved in CO2 and acid signaling in chemosensitive neurons. Am J Physiol Cell Physiol. 2004;287:C1493–C1526. [PubMed]
  • Rajan S, Wischmeyer E, Xin LG, Preisig-Muller R, Daut J, Karschin A, Derst C. TASK-3, a novel tandem pore domain acid-sensitive K+ channel. An extracellular histiding as pH sensor. J Biol Chem. 2000;275:16650–16657. [PubMed]
  • Rong W, Gourine AV, Cockayne DA, Xiang Z, Ford AP, Spyer KM, Burnstock G. Pivotal role of nucleotide P2X2 receptor subunit of the ATP-gated ion channel mediating ventilatory responses to hypoxia. J Neurosci. 2003;23:11315–11321. [PubMed]
  • Talley EM, Solorzano G, Lei Q, Kim D, Bayliss DA. CNS distribution of members of the two-pore-domain (KCNK) potassium channel family. J Neurosci. 2001;21:7491–7505. [PubMed]
  • Tan ZY, Lu Y, Whiteis CA, Benson CJ, Chapleau MW, Abboud FM. Acid-sensing ion channels contribute to transduction of extracellular acidosis in rat carotid body glomus cells. Circ Res. 2007;101:1009–1019. [PubMed]
  • Washburn CP, Bayliss DA, Guyenet PG. Cardiorespiratory neurons of the rat ventrolateral medulla contain TASK-1 and TASK-3 channel mRNA. Respir Physiol Neurobiol. 2003;138:19–35. [PubMed]
  • Washburn CP, Sirois JE, Talley EM, Guyenet PG, Bayliss DA. Serotonergic raphe neurons express TASK channel transcripts and a TASK-like pH- and halothane-sensitive K+ conductance. J Neurosci. 2002;22:1256–1265. [PubMed]
  • Yamamoto Y, Kummer W, Atoji Y, Suzuki Y. TASK-1, TASK-2, TASK-3 and TRAAK immunoreactivities in the rat carotid body. Brain Res. 2002;950:304–307. [PubMed]
  • Yamamoto Y, Taniguchi K. Immunolocalization of tandem pore domain K+ channels in the rat carotid body. Adv Exp Med Biol. 2006;580:9–14. [PubMed]
  • Zhang M, Zhong H, Vollmer C, Nurse CA. Co-release of ATP and ACh mediates hypoxic signalling at rat carotid body chemoreceptors. J Physiol 525 Pt. 2000;1:143–158. [PubMed]