Osteoprotegerin is a receptor for the cytotoxic ligand TRAIL

被引:1013
作者
Emery, JG
McDonnell, P
Burke, MB
Deen, KC
Lyn, S
Silverman, C
Dul, E
Appelbaum, ER
Eichman, C
DiPrinzio, R
Dodds, RA
James, IE
Rosenberg, M
Lee, JC
Young, PR
机构
[1] SmithKline Beecham Pharmaceut, Dept Mol Biol, King Of Prussia, PA 19406 USA
[2] SmithKline Beecham Pharmaceut, Dept Biol Struct, King Of Prussia, PA 19406 USA
[3] SmithKline Beecham Pharmaceut, Dept Mol & Cellular Immunol, King Of Prussia, PA 19406 USA
[4] SmithKline Beecham Pharmaceut, Dept Prot Biochem, King Of Prussia, PA 19406 USA
[5] SmithKline Beecham Pharmaceut, Dept Gene Express Sci, King Of Prussia, PA 19406 USA
[6] SmithKline Beecham Pharmaceut, Dept Bone & Cartilage Biol, King Of Prussia, PA 19406 USA
[7] SmithKline Beecham Pharmaceut, Dept Antiinfect, Collegeville, PA 19426 USA
关键词
D O I
10.1074/jbc.273.23.14363
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
TRAIL is a tumor necrosis factor-related ligand that induces apoptosis upon binding to its death domain-containing receptors, DR4 and DR5. Two additional TRAIL receptors, TRID/DcR1 and DcR2, lack functional death domains and function as decoy receptors for TRAIL. We have identified a fifth TRAIL receptor, namely osteoprotegerin (OPG), a secreted tumor necrosis factor receptor homologue that inhibits osteoclastogenesis and increases bone density in vivo. OPG-Fc binds TRAIL with an affinity of 3.0 nM, which is slightly weaker than the interaction of TRID-Fc or DR5-Fc with TRAIL. OPG inhibits TRAIL-induced apoptosis of Jurkat cells, Conversely, TRAIL blocks the anti-osteoclastogenic activity of OPG, These data suggest potential cross-regulatory mechanisms by OPG and TRAIL.
引用
收藏
页码:14363 / 14367
页数:5
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