Shedding of CD163, a novel regulatory mechanism for a member of the scavenger receptor cysteine-rich family

被引:138
作者
Droste, A [1 ]
Sorg, C [1 ]
Högger, P [1 ]
机构
[1] Univ Munster, Inst Expt Dermatol, D-48149 Munster, Germany
关键词
D O I
10.1006/bbrc.1999.0294
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
The glucocorticoid-inducible transmembrane protein CD163 is a member of the scavenger receptor cysteine-rich (SRCR) family which is expressed exclusively on human monocytes and macrophages. The expression of the protein is significantly downregulated in response to phorbol 12-myristate 13-acetate (PMA) by a yet unknown mechanism. We now demonstrate that PMA induces shedding of a soluble form of CD163 rather than internalization, revealing a novel regulatory mechanism for a member of the SRCR family. Bisindolylmaleimide I was shown to inhibit phorbol ester-induced shedding, thus implying an involvement of protein kinase C (PKC). Furthermore, cleavage could be prevented by protease inhibitors. Therefore, we suggest that PMA-induced activation of PKC leads to protease-mediated shedding of CD163. These results indicate a specific release mechanism of soluble CD163 by human monocytes which could play an important role in modulating inflammatory processes. (C) 1999 Academic Press.
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页码:110 / 113
页数:4
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