基质金属蛋白酶在发育中的表达与功能。

Z Werb, C M Alexander, R R Adler
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引用次数: 0

摘要

在哺乳动物胚胎发生过程中,细胞外基质(ECM)重构伴随着细胞迁移、细胞间相互作用、胚胎扩张、子宫着床和组织侵袭。我们发现小鼠胚胎表达胶原酶、基质溶解素和金属蛋白酶组织抑制剂(TIMP)的mRNA转录本,并分泌功能性ecm降解金属蛋白酶,包括胶原酶和基质溶解素。这些金属蛋白酶可被TIMP抑制,并在着床周发育和内胚层分化过程中受到调节。在小鼠胚胎着床过程中,通过滋养细胞在其侵袭期分泌蛋白酶和母体蜕膜中TIMP的相互表达,提示了依赖于金属蛋白酶的受控蛋白水解反应的参与。外源性TIMP影响囊胚生长过程中顶壁内胚层细胞的迁移。综上所述,这些数据表明,在哺乳动物发育过程中,金属蛋白酶在细胞- ecm相互作用中起作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Expression and function of matrix metalloproteinases in development.

Extracellular matrix (ECM) remodeling accompanies cell migration, cell-cell interactions, embryo expansion, uterine implantation and tissue invasion during mammalian embryogenesis. We have found that mouse embryos express mRNA transcripts for collagenase, stromelysin and the tissue inhibitor of metalloproteinases (TIMP) and secrete functional ECM-degrading metalloproteinases, including collagenase and stromelysin. These metalloproteinases are inhibitable by TIMP and are regulated during peri-implantation development and endoderm differentiation. The involvement of a controlled proteolytic reaction, dependent on metalloproteinases, during the implantation of mouse embryos is suggested by the secretion of proteinases by trophoblast during its invasive phase and by the reciprocal expression of TIMP in the maternal deciduum. Exogenous TIMP affects the migration of parietal endoderm cells during blastocyst outgrowth in vitro. Taken together, these data suggest that metalloproteinases function in cell-ECM interactions during mammalian development.

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