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早期胚胎发生中的纤溶酶原激活物:滋养层和壁内胚层产生的酶

Plasminogen activator in early embryogenesis: enzyme production by trophoblast and parietal endoderm.

作者信息

Strickland S, Reich E, Sherman M I

出版信息

Cell. 1976 Oct;9(2):231-40. doi: 10.1016/0092-8674(76)90114-8.

Abstract

We have surveyed the early stages in the development and differentiation of cultured mouse embryos for plasminogen activator production. This enzyme is first detectable by the sixth equivalent gestation day. Thereafter, cultured blastocysts produce plasminogen activator with a biphasic time course: in the first phase, enzyme secretion rises to a maximum at about the eighth day and then decreases; a second phase, during which more enzyme accumulates, begins somewhat later and continues to at least the fifteenth day. By fractionating the blastocyst into its constituent cell types, we have identified the trophoblast as the cells responsible for the first phase of enzyme synthesis. The pattern of enzyme production by the trophoblast is closely correlated with the invasive period of these cells in vivo and implies that plasminogen activator is involved in embryo implantation. The second phase of plasminogen activator production is due to parietal endoderm, which initiates enzyme synthesis upon differentiation from the inner cell mass. The properties of the parietal endoderm suggest that plasminogen activator may participate in the migration of these cells and/or in the metabolism of Reichert's membrane which accompanies embryo growth. These results are consistent with the concept, deveolped from work on other cell types, that plasminogen activator may represent a generalized mechanism for tissue remodeling and cell migration.

摘要

我们已经研究了培养的小鼠胚胎在发育和分化早期产生纤溶酶原激活物的情况。在相当于妊娠的第六天首次检测到这种酶。此后,培养的囊胚产生纤溶酶原激活物的过程呈双相时间进程:在第一阶段,酶分泌在大约第八天升至最高水平,然后下降;第二阶段,在此期间更多的酶积累,开始时间稍晚,并至少持续到第十五天。通过将囊胚分离成其组成细胞类型,我们已确定滋养层细胞是负责酶合成第一阶段的细胞。滋养层细胞产生酶的模式与这些细胞在体内的侵入期密切相关,这意味着纤溶酶原激活物参与胚胎着床。纤溶酶原激活物产生的第二阶段归因于壁内胚层,壁内胚层从内细胞团分化时开始启动酶的合成。壁内胚层的特性表明,纤溶酶原激活物可能参与这些细胞的迁移和/或伴随胚胎生长的赖歇特膜的代谢。这些结果与基于对其他细胞类型的研究得出的概念一致,即纤溶酶原激活物可能代表组织重塑和细胞迁移的一种普遍机制。

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