| Literature DB >> 29375126 |
Keqiang Chen1, Zhiyao Bao1,2, Peng Tang1,3, Wanghua Gong4, Teizo Yoshimura5, Ji Ming Wang6.
Abstract
For the past twenty years, chemokines have emerged as a family of critical mediators of cell migration during immune surveillance, development, inflammation and cancer progression. Chemokines bind to seven transmembrane G protein-coupled receptors (GPCRs) that are expressed by a wide variety of cell types and cause conformational changes in trimeric G proteins that trigger the intracellular signaling pathways necessary for cell movement and activation. Although chemokines have evolved to benefit the host, inappropriate regulation or utilization of these small proteins may contribute to or even cause diseases. Therefore, understanding the role of chemokines and their GPCRs in the complex physiological and diseased microenvironment is important for the identification of novel therapeutic targets. This review introduces the functional array and signals of multiple chemokine GPCRs in guiding leukocyte trafficking as well as their roles in homeostasis, inflammation, immune responses and cancer.Entities:
Keywords: GPCRs; chemokines; chemotaxis; diseases; homeostasis; inflammatory cells
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Year: 2018 PMID: 29375126 PMCID: PMC6052829 DOI: 10.1038/cmi.2017.134
Source DB: PubMed Journal: Cell Mol Immunol ISSN: 1672-7681 Impact factor: 11.530