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Proton-Sensing GPCRs in Health and Disease

Journal

CELLS
Volume 10, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/cells10082050

Keywords

proton-sensing GPCR; inflammation; pain; neuropathic pain; GPCR; tumor microenvironment; GPR4; TDAG8; OGR1; G2A

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Funding

  1. Deutsche Forschungsgemeinschaft (German Research Foundation) [SFB1039]
  2. Fraunhofer Foundation
  3. Fraunhofer Cluster of Excellence for Immune-Mediated Diseases (CIMD)

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The proton-sensing G-protein coupled receptors, including GPR4, TDAG8, OGR1, and G2A, act as cellular sensors of acidification with varying pH detection capabilities. While initially thought to detect acidic cellular environments in inflammation, recent studies reveal their diverse roles in tumor biology, cardiovascular physiology, asthma, mechanosensation, and other processes. Each receptor has unique properties and potential roles in various physiological and pathophysiological conditions, highlighting the need for further research on their biological and pharmacological contexts.
The group of proton-sensing G-protein coupled receptors (GPCRs) consists of the four receptors GPR4, TDAG8 (GPR65), OGR1 (GPR68), and G2A (GPR132). These receptors are cellular sensors of acidification, a property that has been attributed to the presence of crucial histidine residues. However, the pH detection varies considerably among the group of proton-sensing GPCRs and ranges from pH of 5.5 to 7.8. While the proton-sensing GPCRs were initially considered to detect acidic cellular environments in the context of inflammation, recent observations have expanded our knowledge about their physiological and pathophysiological functions and many additional individual and unique features have been discovered that suggest a more differentiated role of these receptors in health and disease. It is known that all four receptors contribute to different aspects of tumor biology, cardiovascular physiology, and asthma. However, apart from their overlapping functions, they seem to have individual properties, and recent publications identify potential roles of individual GPCRs in mechanosensation, intestinal inflammation, oncoimmunological interactions, hematopoiesis, as well as inflammatory and neuropathic pain. Here, we put together the knowledge about the biological functions and structural features of the four proton-sensing GPCRs and discuss the biological role of each of the four receptors individually. We explore all currently known pharmacological modulators of the four receptors and highlight potential use. Finally, we point out knowledge gaps in the biological and pharmacological context of proton-sensing GPCRs that should be addressed by future studies.

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