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ADAMTS-1: a metalloproteinase-disintegrin essential for normal growth, fertility, and organ morphology and function.
Shindo, T; Kurihara, H; Kuno, K; Yokoyama, H; Wada, T; Kurihara, Y; Imai, T; Wang, Y; Ogata, M; Nishimatsu, H; Moriyama, N; Oh-hashi, Y; Morita, H; Ishikawa, T; Nagai, R; Yazaki, Y; Matsushima, K.
Afiliação
  • Shindo T; Department of Cardiovascular Medicine, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
J Clin Invest ; 105(10): 1345-52, 2000 May.
Article em En | MEDLINE | ID: mdl-10811842
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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metaloendopeptidases / Desintegrinas / Fertilidade / Crescimento Tipo de estudo: Etiology_studies Limite: Animals / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2000 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Metaloendopeptidases / Desintegrinas / Fertilidade / Crescimento Tipo de estudo: Etiology_studies Limite: Animals / Female / Humans / Male / Pregnancy Idioma: En Ano de publicação: 2000 Tipo de documento: Article