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CD32 expression and signaling is down-regulated by transforming growth factor-beta 1 on human monocytes.

作者信息

Reterink T J, Klar-Mohamad N, Nibbering P H, van Es L A, Daha M R

机构信息

Department of Nephrology, Leiden University Hospital, The Netherlands.

出版信息

Eur J Immunol. 1996 Aug;26(8):1970-3. doi: 10.1002/eji.1830260844.

DOI:10.1002/eji.1830260844
PMID:8765047
Abstract

CD32 (Fc gamma RII) is the most abundantly distributed class of IgG Fc receptors in the human body. In this study, we analyzed the effect of transforming growth factor (TGF)-beta 1, a cytokine with strong immunosuppressive function, on the expression and function of CD32 on freshly isolated peripheral blood monocytes and three human monocytic cell lines, U937, THP-1 and Mono mac-6. We found that TGF-beta 1 down-regulates CD32 expression on monocytes and all monocytic cell lines in a dose- and time-dependent fashion. A mean down-regulation of CD32 expression on THP-1 cells of 54 +/- 3.2% after 24 h was found at a concentration of 1 ng/ml TGF-beta 1. At the mRNA level, TGF-beta 1 induced a twofold down-regulation of CD32. Cross-linking of CD32 induced an increase in the concentration of intracellular Ca2+, which was reduced by 50% by TGF-beta 1, suggesting a decreased downstream signaling mediated by the receptor.

摘要

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