| Literature DB >> 26701131 |
Liangzhu Li1, Keqiang Chen1, Yi Xiang1, Teizo Yoshimura1, Shaobo Su1, Jianwei Zhu1, Xiu-wu Bian2, Ji Ming Wang2.
Abstract
Formyl-peptide receptors are a family of 7 transmembrane domain, Gi-protein-coupled receptors that possess multiple functions in many pathophysiologic processes because of their expression in a variety of cell types and their capacity to interact with a variety of structurally diverse, chemotactic ligands. Accumulating evidence demonstrates that formyl-peptide receptors are critical mediators of myeloid cell trafficking in the sequential chemotaxis signal relays in microbial infection, inflammation, and immune responses. Formyl-peptide receptors are also involved in the development and progression of cancer. In addition, one of the formyl-peptide receptor family members, Fpr2, is expressed by normal mouse-colon epithelial cells, mediates cell responses to microbial chemotactic agonists, participates in mucosal development and repair, and protects against inflammation-associated tumorigenesis. These novel discoveries greatly expanded the current understanding of the role of formyl-peptide receptors in host defense and as potential molecular targets for the development of therapeutics. © Society for Leukocyte Biology.Entities:
Keywords: cancer; immunity; inflammation; leukocytes; trafficking
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Year: 2015 PMID: 26701131 PMCID: PMC4750370 DOI: 10.1189/jlb.2RI0815-354RR
Source DB: PubMed Journal: J Leukoc Biol ISSN: 0741-5400 Impact factor: 4.962