Watson A J
Department of Medical Biochemistry, University of Calgary Health Sciences Center, Alberta, Canada.
Mol Reprod Dev. 1992 Dec;33(4):492-504. doi: 10.1002/mrd.1080330417.
Preimplantation development encompasses the "free"-living period of mammalian embryogenesis, which culminates in the formation of a fluid-filled structure, the blastocyst. Cavitation (blastocyst formation) is accompanied by the expression of a novel set of gene products that contribute directly to the attainment of cell polarity with the trophectoderm, which is both the first epithelium of development and the outer cell layer encircling the inner cell mass of the blastocyst. Several of these gene products have been identified and include the tight junction (ZO-1), Na/K-ATPase (alpha and beta subunits), uvomorulin, gap junction (connexin43), and growth factors such as transforming growth factor-alpha (TGF-alpha) and epidermal growth factor (EGF). This review will examine the role(s) of each of these gene products during the onset and progression of blastocyst formation. The trophectodermal tight junctional permeability seal regulates the leakage of blastocoel fluid and also assists in the maintenance of a polarized Na/K-ATPase distribution to the basolateral plasma membrane domain of the mural trophectoderm. The polarized distribution of the Na/K-ATPase plays an integral role in the establishment of a trans-trophectoderm Na+ gradient, which drives the osmotic accumulation of water across the epithelium into the nascent blastocoelic cavity. The cell adhesion provided by uvomorulin is necessary for the establishment of the tight junctional seal, as well as the maintenance of the polarized Na/K-ATPase distribution. Growth factors such as TGF-alpha and EGF stimulate an increase in the rate of blastocoel expansion, which could, in part, be mediated by secondary messengers that result in an increase in Na/K-ATPase activity. Insight into the mechanism of cavitation has, therefore, directly linked blastocyst formation to trophectoderm cell differentiation, which arises through fundamental cell biological processes that are directly involved in the attainment of epithelial cell polarity.
植入前发育涵盖了哺乳动物胚胎发生的“自由”生活期,最终形成一个充满液体的结构——囊胚。空化(囊胚形成)伴随着一组新的基因产物的表达,这些产物直接有助于滋养外胚层实现细胞极性,滋养外胚层既是发育过程中的第一个上皮层,也是围绕囊胚内细胞团的外层细胞层。其中一些基因产物已被鉴定出来,包括紧密连接蛋白(ZO-1)、钠钾ATP酶(α和β亚基)、桥粒芯蛋白、缝隙连接蛋白(连接蛋白43),以及生长因子,如转化生长因子-α(TGF-α)和表皮生长因子(EGF)。本综述将探讨这些基因产物在囊胚形成的起始和进展过程中的作用。滋养外胚层紧密连接的通透性密封调节囊胚腔液的渗漏,还有助于维持钠钾ATP酶在壁滋养外胚层基底外侧质膜结构域的极化分布。钠钾ATP酶的极化分布在建立跨滋养外胚层的钠离子梯度中起着不可或缺的作用,该梯度驱动水通过上皮细胞渗透积聚到新生的囊胚腔中。桥粒芯蛋白提供的细胞黏附对于紧密连接密封的建立以及钠钾ATP酶极化分布的维持是必要的。诸如TGF-α和EGF等生长因子刺激囊胚腔扩张速率增加,这可能部分由导致钠钾ATP酶活性增加的第二信使介导。因此,对空化机制的深入了解已将囊胚形成与滋养外胚层细胞分化直接联系起来,滋养外胚层细胞分化是通过直接参与上皮细胞极性获得的基本细胞生物学过程产生的。