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Purinergic signalling mediates bidirectional crosstalk between chemoreceptor type I and glial‐like type II cells of the rat carotid body
Author(s) -
Murali Sindhubarathi,
Nurse Colin A.
Publication year - 2015
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jp271494
Subject(s) - purinergic receptor , carotid body , pannexin , microbiology and biotechnology , p2 receptor , chemoreceptor , purinergic signalling , chemistry , apyrase , biology , receptor , medicine , adenosine receptor , endocrinology , stimulation , intracellular , biochemistry , extracellular , gap junction , connexin , agonist
Key points Carotid body chemoreceptors are organized in clusters containing receptor type I and contiguous glial‐like type II cells. While type I cells depolarize and release ATP during chemostimulation, the role of type II cells which express purinergic P2Y2 receptors (P2Y2Rs) and ATP‐permeable pannexin‐1 (Panx‐1) channels, is unclear. Here, we show that in isolated rat chemoreceptor clusters, type I cell depolarization induced by hypoxia, hypercapnia, or high K + caused delayed intracellular Ca 2+ elevations (Δ[Ca 2+ ] i ) in nearby type II cells that were inhibited by the P2Y2R blocker suramin, or by the nucleoside hydrolase apyrase. Likewise, stimulation of P2Y2Rs on type II cells caused a delayed, secondary Δ[Ca 2+ ] i in nearby type I cells that was inhibited by blockers of Panx‐1 channels, adenosine A 2A receptors and 5′‐ectonucleotidase. We propose that reciprocal crosstalk between type I and type II cells contributes to sensory processing in the carotid body via purinergic signalling pathways.Abstract The mammalian carotid body (CB) is excited by blood‐borne stimuli including hypoxia and acid hypercapnia, leading to respiratory and cardiovascular reflex responses. This chemosensory organ consists of innervated clusters of receptor type I cells, ensheathed by processes of adjacent glial‐like type II cells. ATP is a major excitatory neurotransmitter released from type I cells and type II cells express purinergic P2Y2 receptors (P2Y2Rs), the activation of which leads to the opening of ATP‐permeable, pannexin‐1 (Panx‐1) channels. While these properties support crosstalk between type I and type II cells during chemotransduction, direct evidence is lacking. To address this, we first exposed isolated rat chemoreceptor clusters to acute hypoxia, isohydric hypercapnia, or the depolarizing stimulus high K + , and monitored intracellular [Ca 2+ ] using Fura‐2. As expected, these stimuli induced intracellular [Ca 2+ ] elevations (Δ[Ca 2+ ] i ) in type I cells. Interestingly, however, there was often a delayed, secondary Δ[Ca 2+ ] i in nearby type II cells that was reversibly inhibited by the P2Y2R antagonist suramin, or by the nucleoside hydrolase apyrase. By contrast, type II cell stimulation with the P2Y2R agonist uridine‐5′‐triphosphate (100 μ m ) often led to a delayed, secondary Δ[Ca 2+ ] i response in nearby type I cells that was reversibly inhibited by the Panx‐1 blocker carbenoxolone (5 μ m ). This Δ[Ca 2+ ] i response was also strongly inhibited by blockers of either the adenosine A 2A receptor (SCH 58261) or of the 5′‐ectonucleotidase (AOPCP), suggesting it was due to adenosine arising from breakdown of ATP released through Panx‐1 channels. Collectively, these data strongly suggest that purinergic signalling mechanisms mediate crosstalk between CB chemoreceptor and glial cells during chemotransduction.