ADAMTS-1: a metalloproteinase-disintegrin essential for normal growth, fertility, and organ morphology and function

被引:273
作者
Shindo, T
Kurihara, H
Kuno, K
Yokoyama, H
Wada, T
Kurihara, Y
Imai, T
Wang, YH
Ogata, M
Nishimatsu, H
Moriyama, N
Oh-hashi, Y
Morita, H
Ishikawa, T
Nagai, R
Yazaki, Y
Matsushima, K
机构
[1] Univ Tokyo, Grad Sch Med, Dept Cardiovasc Med, Bunkyo Ku, Tokyo 1138655, Japan
[2] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Tokyo, Japan
[3] Kanazawa Univ, Div Blood Purificat, Sch Med, Kanazawa, Ishikawa 920, Japan
[4] Kanazawa Univ, Dept Internal Med 1, Sch Med, Kanazawa, Ishikawa 920, Japan
[5] Univ Tokyo, Grad Sch Med, Dept Pathol, Tokyo, Japan
[6] Hosp Int Med Ctr Japan, Tokyo, Japan
[7] Univ Tokyo, Grad Sch Med, Dept Mol Prevent Med, Tokyo, Japan
关键词
D O I
10.1172/JCI8635
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A disintegrin and metalloproteinase (ADAM) represents a protein family possessing both metalloproteinase and disintegrin domains. ADAMTS-1, an ADAM family member cloned from cachexigenic colon adenocarcinoma, is unusual in that it contains thrombospondin type I motifs and anchors to the extracellular matrix. To elucidate the biological role of ADAMTS-1, we developed ADAMTS-1-null mice by gene targeting, Targeted disruption of the mouse ADAMTS-1 gene resulted in growth retardation with adipose tissue malformation, Impaired female fertilization accompanied by histological changes in the uterus and ovaries also resulted, Furthermore, ADAMTS-1(-/-) mice demonstrated enlarged renal calices with fibrotic changes from the ureteropelvic junction through the ureter, and abnormal adrenal medullary architecture without capillary formation. ADAMTS-1 thus appears necessary for normal growth, fertility, and organ morphology and function. Moreover, the resemblance of the renal phenotype to human ureteropelvic junction obstruction may provide a clue to the pathogenesis of this common congenital disease.
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收藏
页码:1345 / 1352
页数:8
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