Regulation of no synthesis induced by inflammatory mediators in RAW264.7 cells: Collagen prevents inhibitory by osteopontin

被引:18
作者
Tian, JY
Sorensen, ES
Butler, WT
Lopez, CA
Sy, MS
Desai, NK
Denhardt, DT
机构
[1] Rutgers State Univ, Nelson Labs, Dept Cell Biol & Neurosci, Piscataway, NJ 08854 USA
[2] Aarhus Univ, Prot Chem Lab, DK-8000 Aarhus C, Denmark
[3] Univ Texas, Hlth Sci Ctr, Dept Basic Sci, Dent Branch, Houston, TX 77030 USA
[4] Case Western Reserve Univ, Sch Med, Dept Pathol, Cleveland, OH 44106 USA
关键词
macrophages; cell signalling; extracellular matrix; integrins; hyaluronate;
D O I
10.1006/cyto.1999.0634
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
Osteopontin has been shown to inhibit the induction of inducible nitric oxide synthase (iNOS, or NOS2) by lipopolysaccharide and interferon-gamma in the RAW264.7 mouse monocyte/macrophage line and in primary mouse proximal tubule epithelial cells. However, the RAW264.7 cells become refractory to the action of OPN after several subcultures or under dilute culture conditions, possibly because of changes in the composition of the extraacellular matrix. We make this suggestion because if the cells are plated on a collagen type I or collagen type IV substrate the inhibitory action of OPN is completely suppressed; this is not the case on substrates consisting of laminin, fibronectin, poly-D-lysine, or poly-(2-hydroxyethylmethylacrylate). These observations imply that macrophages are sensitive to regulation by OPN only in certain physiological contexts. Both hyaluronate, which binds CD44, and rat IgCs are also able to inhibit the induction of NO synthesis by the inflammatory mediators. The similar actions of HA and OPN are consistent with the possibility that CD44 may be a receptor for OPN. (C) 2000 Academic Press.
引用
收藏
页码:450 / 457
页数:8
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