期刊
JOURNAL OF CELLULAR BIOCHEMISTRY
卷 102, 期 4, 页码 912-924出版社
WILEY
DOI: 10.1002/jcb.21558
关键词
integrins; CD44; apoptosis; phosphorylation; beta sheet
资金
- NIAMS NIH HHS [AR 44434] Funding Source: Medline
- NIEHS NIH HHS [ES 06897] Funding Source: Medline
Osteopontin (OPN) plays roles in a variety of cellular processes from bone resorption and extracellular matrix (ECM) remodeling to immune cell activation and inhibition of apoptosis. Because it binds receptors (integrins, CD44 variants) typically engaged by ECM molecules, OPN acts as a soluble ECM molecule. A persistent theme throughout the characterization of how OPN functions has been the importance of phosphorylation. The source of the OPN used in specific experiments and the location of modified sites is an increasingly important consideration for OPN research. We review briefly some of the ways OPN impacts on the biology of mammalian systems with an emphasis on the importance of serine phosphorylation in modulating its signaling ability. We describe experiments that support the hypothesis that differences in the post-translational phosphorylation of OPN expressed by different cell types regulate how it impacts on target cells. Analyses of OPN's potential secondary structure reveal a possible beta-sheet conformation that offers an interpretation of certain experimental observations, specifically the effect of thrombin cleavage; it is consistent with an interaction between the C-terminal region of the protein and the central integrin-binding RGD sequence.
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