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
相关论文
共 30 条
[11]   MALE-FEMALE DIFFERENCES IN FERTILITY AND BLOOD-PRESSURE IN ACE-DEFICIENT MICE [J].
KREGE, JH ;
JOHN, SWM ;
LANGENBACH, LL ;
HODGIN, JB ;
HAGAMAN, JR ;
BACHMAN, ES ;
JENNETTE, JC ;
OBRIEN, DA ;
SMITHIES, O .
NATURE, 1995, 375 (6527) :146-148
[12]  
Kuno K, 1997, J BIOL CHEM, V272, P556, DOI 10.1074/jbc.272.1.556
[13]   ADAMTS-1 protein anchors at the extracellular matrix through the thrombospondin type I motifs and its spacing region [J].
Kuno, K ;
Matsushima, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (22) :13912-13917
[14]   ADAMTS-1 is an active metalloproteinase associated extracellular matrix [J].
Kuno, K ;
Terashima, Y ;
Matsushima, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (26) :18821-18826
[15]   The exon/intron organization and chromosomal mapping of the mouse ADAMTS-1 gene encoding an ADAM family protein with TSP motifs [J].
Kuno, K ;
Iizasa, H ;
Ohno, S ;
Matsushima, K .
GENOMICS, 1997, 46 (03) :466-471
[16]   Angiotensin induces the urinary peristaltic machinery during the perinatal period [J].
Miyazaki, Y ;
Tsuchida, S ;
Nishimura, H ;
Pope, JC ;
Harris, RC ;
McKanna, JM ;
Inagami, T ;
Hogan, BLM ;
Fogo, A ;
Ichikawa, I .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 102 (08) :1489-1497
[17]   Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha [J].
Moss, ML ;
Jin, SLC ;
Milla, ME ;
Burkhart, W ;
Carter, HL ;
Chen, WJ ;
Clay, WC ;
Didsbury, JR ;
Hassler, D ;
Hoffman, CR ;
Kost, TA ;
Lambert, MH ;
Leesnitzer, MA ;
McCauley, P ;
McGeehan, G ;
Mitchell, J ;
Moyer, M ;
Pahel, G ;
Rocque, W ;
Overton, LK ;
Schoenen, F ;
Seaton, T ;
Su, JL ;
Warner, J ;
Willard, D ;
Becherer, JD .
NATURE, 1997, 385 (6618) :733-736
[18]   Structural changes of collagen components and diminution of nerves in congenital ureteropelvic junction obstruction [J].
Murakumo, M ;
Nonomura, K ;
Yamashita, T ;
Ushiki, T ;
Abe, K ;
Koyanagi, T .
JOURNAL OF UROLOGY, 1997, 157 (05) :1963-1968
[19]   Gene targeting in mice reveals a requirement for angiotensin in the development and maintenance of kidney morphology and growth factor regulation [J].
Niimura, F ;
Labosky, PA ;
Kakuchi, J ;
Okubo, S ;
Yoshida, H ;
Oikawa, T ;
Ichiki, T ;
Naftilan, AJ ;
Fogo, A ;
Inagami, T ;
Hogan, BLM ;
Ichikawa, I .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 96 (06) :2947-2954
[20]   Angiotensinogen gene null-mutant mice lack homeostatic regulation of glomerular filtration and tubular reabsorption [J].
Okubo, S ;
Niimura, F ;
Matsusaka, T ;
Fogo, A ;
Hogan, BLM ;
Ichikawa, I .
KIDNEY INTERNATIONAL, 1998, 53 (03) :617-625