ADAM10 is a principal 'sheddase' of the low-affinity immunoglobulin E receptor CD23

被引:167
作者
Weskamp, Gisela
Ford, Jill W.
Sturgill, Jamie
Martin, Steve
Docherty, Andrew J. P.
Swendeman, Steven
Broadway, Neil
Hartmann, Dieter
Saftig, Paul
Umland, Shelby
Sehara-Fujisawa, Atsuko
Black, Roy A.
Ludwig, Andreas
Becherer, J. David
Conrad, Daniel H.
Blobel, Carl P. [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Hosp Special Surg, Arthrit & Tissue Regenerat Program, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Dept Med, New York, NY 10021 USA
[3] Cornell Univ, Weill Med Coll, Dept Physiol & Biophys, New York, NY 10021 USA
[4] Virginia Commonwealth Univ, Dept Immunol & Microbiol, Richmond, VA 23298 USA
[5] GlaxoSmithKline, Discovery Res, Stevenage SG1 2NY, Herts, England
[6] Celltech Ltd, Slough SL1 4EN, Berks, England
[7] Katholieke Univ Leuven VIB, Dept Human Genet, B-3000 Louvain, Belgium
[8] Univ Kiel, Inst Biochem, D-24089 Kiel, Germany
[9] Schering Plough Corp, Inst Res, Kenilworth, NJ 07033 USA
[10] Kyoto Univ, Inst Frontier Med Sci, Dept Growth Regulat, Kyoto 6068507, Japan
[11] Amgen Inc, Seattle, WA 98119 USA
[12] Rhein Westphalian Tech Univ, Inst Mol Cardiovasc Res, Aachen, Germany
[13] GlaxoSmithKline, Dept Biochem & Analyt Pharmacol, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1038/ni1399
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD23, the low-affinity immunoglobulin E receptor, is an important modulator of the allergic response and of diseases such as rheumatoid arthritis. The proteolytic release of CD23 from cells is considered a key event in the allergic response. Here we used loss-of-function and gain-of-function experiments with cells lacking or overexpressing candidate CD23-releasing enzymes (ADAM8, ADAM9, ADAM10, ADAM12, ADAM15, ADAM17, ADAM19 and ADAM33), ADAM-knockout mice and a selective inhibitor to identify ADAM10 as the main CD23-releasing enzyme in vivo. Our findings provide a likely target for the treatment 5 of allergic reactions and set the stage for further studies of the involvement of ADAM10 in CD23-dependent pathologies.
引用
收藏
页码:1293 / 1298
页数:6
相关论文
共 46 条
  • [31] MARKED AMELIORATION OF ESTABLISHED COLLAGEN-INDUCED ARTHRITIS BY TREATMENT WITH ANTIBODIES TO CD23 IN-VIVO
    PLATERZYBERK, C
    BONNEFOY, JY
    [J]. NATURE MEDICINE, 1995, 1 (08) : 781 - 785
  • [32] ADAM10 cleavage of N-cadherin and regulation of cell-cell adhesion and β-catenin nuclear signalling
    Reiss, K
    Maretzky, T
    Ludwig, A
    Tousseyn, T
    de Strooper, B
    Hartmann, D
    Saftig, P
    [J]. EMBO JOURNAL, 2005, 24 (04) : 742 - 752
  • [33] Increased synovial fluid levels of soluble CD23 are associated with an erosive status in rheumatoid arthritis (RA)
    Ribbens, C
    Bonnet, V
    Kaiser, MJ
    Andre, B
    Kaye, O
    Franchimont, N
    De Groote, D
    Beguin, Y
    Malaise, MG
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2000, 120 (01) : 194 - 199
  • [34] Metalloprotease-disintegrin MDC9: Intracellular maturation and catalytic activity
    Roghani, M
    Becherer, JD
    Moss, ML
    Atherton, RE
    Erdjument-Bromage, H
    Arribas, J
    Blackburn, RK
    Weskamp, G
    Tempst, P
    Blobel, CP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) : 3531 - 3540
  • [35] KUZ, a conserved metalloprotease-disintegrin protein with two roles in Drosophila neurogenesis
    Rooke, J
    Pan, D
    Xu, T
    Rubin, GM
    [J]. SCIENCE, 1996, 273 (5279) : 1227 - 1231
  • [36] Anti-CD23
    Rosenwasser, LJ
    Meng, JF
    [J]. CLINICAL REVIEWS IN ALLERGY & IMMUNOLOGY, 2005, 29 (01) : 61 - 72
  • [37] Distinct roles for ADAM10 and ADAM17 in ectodomain shedding of six EGFR ligands
    Sahin, U
    Weskamp, G
    Kelly, K
    Zhou, HM
    Higashiyama, S
    Peschon, J
    Hartmann, D
    Saftig, P
    Blobel, CP
    [J]. JOURNAL OF CELL BIOLOGY, 2004, 164 (05) : 769 - 779
  • [38] Sarfati M, 1996, BLOOD, V88, P4259
  • [39] Schwartz W., 2004, BIOPROCESSING J, V3, P53
  • [40] The ADAMs family of metalloproteases: multidomain proteins with multiple functions
    Seals, DF
    Courtneidge, SA
    [J]. GENES & DEVELOPMENT, 2003, 17 (01) : 7 - 30