Metalloprotease-disintegrin ADAM8: Expression analysis and targeted deletion in mice

被引:96
作者
Kelly, K
Hutchinson, G
Nebenius-Oosthuizen, D
Smith, AJH
Bartsch, JW
Horiuchi, K
Rittger, A
Manova, K
Docherty, AJP
Blobel, CP
机构
[1] Cornell Univ, Weill Med Coll, Hosp Special Surg, Arthritis & Tissue Degenerat Program, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Hosp Special Surg, Cell Biol Program, New York, NY 10021 USA
[3] Sloan Kettering Inst, Cell Biol Program, New York, NY USA
[4] Celltech R&D, Slough, Berks, England
[5] Univ Edinburgh, Inst Stem Cell Res, Gene Targeting Lab, Edinburgh EH8 9YL, Midlothian, Scotland
[6] Univ Bielefeld, D-4800 Bielefeld, Germany
[7] Sloan Kettering Inst, Mol Cytol Core Facil, New York, NY USA
关键词
metalloprotease-disintegrin; ADAM; MS2; CD156a; lymphatic development;
D O I
10.1002/dvdy.20221
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
ADAMS (a disintegrin and metalloprotease 8, also referred to as MS2/CD156a) is a membrane-anchored metalloprotease that was first identified in a macrophage cell line and has been implicated in neurodegenerative diseases. Here, we evaluated the expression of ADAMS during mouse development and generated mice lacking ADAMS (Adam8-/- mice). During early mouse development, ADAMS is expressed by maternal cells in the decidua and by trophoblast derivatives of the embryo but not in the derivatives of the inner cell mass. At later stages, prominent expression of ADAMS is seen in the embryo proper, in the gonadal ridge, thymus, developing cartilage and bone, brain and spinal cord, and in the mesenchyme in close proximity to the branch point between the jugular vein and developing lymphatic vessels. Examination of Adam8-/- mice, however, revealed no major defects in these or other structures during development or in adult tissues and no evident pathological phenotypes. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:221 / 231
页数:11
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