A novel G-protein-coupled receptor-signaling platform and its targeted translation in human disease

被引:21
|
作者
Abdulkhalek, Samar [1 ]
Hrynyk, Michael [2 ]
Szewczuk, Myron R. [1 ]
机构
[1] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
[2] Queens Univ, Dept Chem Engn, Kingston, ON, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
G-protein-coupled receptors; toll-like receptors; receptor tyrosine kinase; glycosylation; Neu1; sialidase; matrix metalloproteinase 9;
D O I
10.2147/RRBC.S28430
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Molecular-targeted G-protein-coupled receptor (GPCR) signaling in human disease has become an important area of scientific and medical research. The interactions between GPCRs with their large number of different G-protein subunits and the large number of glycosylated receptors involved in human diseases are quite diverse. One GPCR is capable of interacting with more than one G protein to initiate multifunctional signaling. However, the activation of a number of GPCRs does not always lead to a direct effect alone on a particular signaling pathway, but rather to an amplification of the response produced by a separate circumstantial signal within the cell. This cross talk among different GPCR transduction signals is a focus of intense research. In this review, evidence exposing the invisible link connecting ligand-binding and receptor activation to a novel GPCR-signaling platform will be reviewed in relation to human disease.
引用
收藏
页码:17 / 30
页数:14
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