| Literature DB >> 10811842 |
T Shindo1, H Kurihara, K Kuno, H Yokoyama, T Wada, Y Kurihara, T Imai, Y Wang, M Ogata, H Nishimatsu, N Moriyama, Y Oh-hashi, H Morita, T Ishikawa, R Nagai, Y Yazaki, K Matsushima.
Abstract
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.Entities:
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Year: 2000 PMID: 10811842 PMCID: PMC315464 DOI: 10.1172/JCI8635
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808