Abstract
The hypoxic ventilatory response (HVR) is critical to breathing and thus oxygen supply to the body and is primarily mediated by the carotid bodies. Here we reveal that carotid body afferent discharge during hypoxia and hypercapnia is determined by the expression of Liver Kinase B1 (LKB1), the principal kinase that activates the AMP-activated protein kinase (AMPK) during metabolic stresses. Conversely, conditional deletion in catecholaminergic cells of AMPK had no effect on carotid body responses to hypoxia or hypercapnia. By contrast, the HVR was attenuated by LKB1 and AMPK deletion. However, in LKB1 knockouts hypoxia evoked hypoventilation, apnoea and Cheyne-Stokes-like breathing, while only hypoventilation and apnoea were observed after AMPK deletion. We therefore identify LKB1 as an essential regulator of carotid body chemosensing and uncover a divergence in dependency on LKB1 and AMPK between the carotid body on one hand and the HVR on the other.
Original language | English |
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Article number | 642 |
Number of pages | 15 |
Journal | Communications Biology |
Volume | 5 |
Issue number | 1 |
DOIs | |
Publication status | Published - 29 Jun 2022 |
Keywords
- AMP-Activated Protein Kinases/genetics
- Apnea
- Carotid Body/metabolism
- Humans
- Hypercapnia/metabolism
- Hypoventilation/metabolism
- Hypoxia/metabolism
ASJC Scopus subject areas
- General Agricultural and Biological Sciences
- General Biochemistry,Genetics and Molecular Biology
- Medicine (miscellaneous)