| Literature DB >> 28950945 |
Hsi-Hsien Lin1, Cheng-Chih Hsiao2, Caroline Pabst3, Josée Hébert4, Torsten Schöneberg5, Jörg Hamann6.
Abstract
The adhesion family comprises one of the five major clades of G protein-coupled receptors (GPCRs). Unlike conventional GPCRs, adhesion GPCRs (aGPCRs) have extended ectodomains with various protein folds that facilitate protein-protein interactions and, hence, putative cellular adhesive functions. Juxtaposed to the seven-pass transmembrane domain is a GPCR autoproteolysis-inducing domain that enables autoproteolytic cleavage of the receptor, resulting in a bipartite structure of many aGPCRs. aGPCRs are widely distributed and play critical roles in many developmental processes; yet, the underlying mechanisms of activation and signal transduction have emerged only recently. About one-third of the 33 human aGPCRs are expressed in hematopoietic stem, progenitor, or mature cells, where they define distinct cellular populations. Recent studies have demonstrated roles of aGPCR in the control of innate effector functions and the susceptibility for and onset of (auto)inflammatory conditions. We here discuss the current knowledge about aGPCRs in the regulation of immune responses and inflammation.Entities:
Keywords: Adaptive; Adhesion GPCRs; Immunity; Inflammation; Innate; Signaling
Mesh:
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Year: 2017 PMID: 28950945 DOI: 10.1016/bs.ai.2017.05.005
Source DB: PubMed Journal: Adv Immunol ISSN: 0065-2776 Impact factor: 3.543