1. Tissue-specific mitochondrial HIGD1C promotes oxygen sensitivity in carotid body chemoreceptors.
- Author
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Timón-Gómez, Alba, Scharr, Alexandra L, Wong, Nicholas Y, Ni, Erwin, Roy, Arijit, Liu, Min, Chau, Julisia, Lampert, Jack L, Hireed, Homza, Kim, Noah S, Jan, Masood, Gupta, Alexander R, Day, Ryan W, Gardner, James M, Wilson, Richard JA, Barrientos, Antoni, and Chang, Andy J
- Subjects
Carotid Body ,Mitochondria ,Animals ,Mammals ,Oxygen ,Chemoreceptor Cells ,Hypoxia ,biochemistry ,carotid body ,chemical biology ,human ,mitochondria ,mouse ,neuroscience ,oxygen sensing ,rat ,Neurosciences ,1.1 Normal biological development and functioning ,Underpinning research ,Generic health relevance ,Human ,Mouse ,Rat ,Biochemistry and Cell Biology - Abstract
Mammalian carotid body arterial chemoreceptors function as an early warning system for hypoxia, triggering acute life-saving arousal and cardiorespiratory reflexes. To serve this role, carotid body glomus cells are highly sensitive to decreases in oxygen availability. While the mitochondria and plasma membrane signaling proteins have been implicated in oxygen sensing by glomus cells, the mechanism underlying their mitochondrial sensitivity to hypoxia compared to other cells is unknown. Here, we identify HIGD1C, a novel hypoxia-inducible gene domain factor isoform, as an electron transport chain complex IV-interacting protein that is almost exclusively expressed in the carotid body and is therefore not generally necessary for mitochondrial function. Importantly, HIGD1C is required for carotid body oxygen sensing and enhances complex IV sensitivity to hypoxia. Thus, we propose that HIGD1C promotes exquisite oxygen sensing by the carotid body, illustrating how specialized mitochondria can be used as sentinels of metabolic stress to elicit essential adaptive behaviors.
- Published
- 2022