Bicarbonate signalling via G protein-coupled receptor regulates ischaemia-reperfusion injury

Nat Commun. 2024 Feb 27;15(1):1530. doi: 10.1038/s41467-024-45579-3.

Abstract

Homoeostatic regulation of the acid-base balance is essential for cellular functional integrity. However, little is known about the molecular mechanism through which the acid-base balance regulates cellular responses. Here, we report that bicarbonate ions activate a G protein-coupled receptor (GPCR), i.e., GPR30, which leads to Gq-coupled calcium responses. Gpr30-Venus knock-in mice reveal predominant expression of GPR30 in brain mural cells. Primary culture and fresh isolation of brain mural cells demonstrate bicarbonate-induced, GPR30-dependent calcium responses. GPR30-deficient male mice are protected against ischemia-reperfusion injury by a rapid blood flow recovery. Collectively, we identify a bicarbonate-sensing GPCR in brain mural cells that regulates blood flow and ischemia-reperfusion injury. Our results provide a perspective on the modulation of GPR30 signalling in the development of innovative therapies for ischaemic stroke. Moreover, our findings provide perspectives on acid/base sensing GPCRs, concomitantly modulating cellular responses depending on fluctuating ion concentrations under the acid-base homoeostasis.

MeSH terms

  • Animals
  • Bicarbonates
  • Brain Ischemia*
  • Calcium / metabolism
  • Male
  • Mice
  • Receptors, Estrogen / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Reperfusion Injury*
  • Stroke*

Substances

  • Bicarbonates
  • Calcium
  • Receptors, Estrogen
  • Receptors, G-Protein-Coupled