The TNF receptor superfamily - Role in immune inflammation and bone formation

被引:16
作者
Cheng, X [1 ]
Kinosaki, M [1 ]
Murali, R [1 ]
Greene, MI [1 ]
机构
[1] Univ Penn, Dept Pathol & Lab Med, Abramson Inst Canc Res, Philadelphia, PA 19104 USA
关键词
osteoclastogenesis; RANK/RANKL/TNF/TNFR superfamily molecules; peptidomimetics;
D O I
10.1385/IR:27:2-3:287
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tumor necrosis factor (TNF) and TNF receptor (TNFR) family proteins play important roles in many biological processes. Recently, the TNF-family molecule, RANKL (also called TRANCE, ODF, and OPGL), and its receptors, RANK and OPG, were found to be regulators of the development and activation of osteoclasts in bone remodeling. TNFalpha also activates osteoclasts both by themselves and in synergy with RANKL. We used structure-based design to create peptidomimetics and organic therapeutics that inhibit osteoclastogenesis by inhibiting the interaction of ligands and receptors. Here we show for the first time that blocking TNFa by these small molecules effectively inhibited osteoclast formation in vitro. These mimetics can be used as a probe to understand the molecular basis of osteoclastogenesis and also as a platform to create useful therapeutic agent.
引用
收藏
页码:287 / 294
页数:8
相关论文
共 59 条
[1]   Osteoclastogenesis inhibitory factor suppresses osteoclast survival by intetfering in the interaction of stromal cells with osteoclast [J].
Akatsu, T ;
Murakami, T ;
Nishikawa, M ;
Ono, K ;
Shinomiya, N ;
Tsuda, E ;
Mochizuki, S ;
Yamaguchi, K ;
Kinosaki, M ;
Higashio, K ;
Yamamoto, M ;
Motoyoshi, K ;
Nagata, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 250 (02) :229-234
[2]   A homologue of the TNF receptor and its ligand enhance T-cell growth and dendritic-cell function [J].
Anderson, DM ;
Maraskovsky, E ;
Billingsley, WL ;
Dougall, WC ;
Tometsko, ME ;
Roux, ER ;
Teepe, MC ;
DuBose, RF ;
Cosman, D ;
Galibert, L .
NATURE, 1997, 390 (6656) :175-179
[3]   Commitment and differentiation of osteoclast precursor cells by the sequential expression of c-Fms and receptor activator of nuclear factor κB (RANK) receptors [J].
Arai, F ;
Miyamoto, T ;
Ohneda, O ;
Inada, T ;
Sudo, T ;
Brasel, K ;
Miyata, T ;
Anderson, DM ;
Suda, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (12) :1741-1754
[4]   Death receptors: Signaling and modulation [J].
Ashkenazi, A ;
Dixit, VM .
SCIENCE, 1998, 281 (5381) :1305-1308
[5]   CRYSTAL-STRUCTURE OF THE SOLUBLE HUMAN 55 KD TNF RECEPTOR-HUMAN TNF-BETA COMPLEX - IMPLICATIONS FOR TNF RECEPTOR ACTIVATION [J].
BANNER, DW ;
DARCY, A ;
JANES, W ;
GENTZ, R ;
SCHOENFELD, HJ ;
BROGER, C ;
LOETSCHER, H ;
LESSLAUER, W .
CELL, 1993, 73 (03) :431-445
[6]   Disabling ErbB receptors with rationally designed exocyclic mimetics of antibodies: Structure-function analysis [J].
Berezov, A ;
Zhang, HT ;
Greene, MI ;
Murali, R .
JOURNAL OF MEDICINAL CHEMISTRY, 2001, 44 (16) :2565-2574
[7]   Crystal structure of TRAIL-DR5 complex identifies a critical role of the unique frame insertion in conferring recognition specificity [J].
Cha, SS ;
Sung, BJ ;
Kim, YA ;
Song, YL ;
Kim, HJ ;
Kim, S ;
Lee, MS ;
Oh, BH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (40) :31171-31177
[8]   Osteoprotegerin is a receptor for the cytotoxic ligand TRAIL [J].
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 .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (23) :14363-14367
[9]   The osteoclast differentiation factor osteoprotegerin-ligand is essential for mammary gland development [J].
Fata, JE ;
Kong, YY ;
Li, J ;
Sasaki, T ;
Irie-Sasaki, J ;
Moorehead, RA ;
Elliott, R ;
Scully, S ;
Voura, EB ;
Lacey, DL ;
Boyle, WJ ;
Khokha, R ;
Penninger, JM .
CELL, 2000, 103 (01) :41-50
[10]   TNFa potently activates osteoclasts, through a direct action independent of and strongly synergistic with RANKL [J].
Fuller, K ;
Murphy, C ;
Kirstein, B ;
Fox, SW ;
Chambers, TJ .
ENDOCRINOLOGY, 2002, 143 (03) :1108-1118