Orth J M, Jester W F
Department of Anatomy and Cell Biology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140, USA.
J Androl. 1995 Sep-Oct;16(5):389-99.
During neonatal development of the rat testis, gonocytes resume mitosis and display renewed motility to migrate toward the basal lamina, two events that occur in vitro when these cells are cocultured with Sertoli cells. However, although substantial evidence suggests that development of gonocytes depends on Sertoli cells, little is known of how these cell types interact beyond our previous observations that they communicate via gap junctions and adhere avidly to each other. In the present study, we utilized several approaches to examine the mechanism by which gonocytes adhere to Sertoli cells in vitro. First, we characterized this attachment in general by (1) determining its susceptibility to brief trypsinization in decreasing concentrations of Ca2+, (2) assessing the ability of gonocytes to adhere to Sertoli cells at reduced temperature, and (3) examining the effect of phospholipase C treatment on the number of gonocytes attached to a Sertoli cell monolayer. Because the findings suggested that a non-cadherin mechanism is involved, we used immunofluorescence to identify the presence of neural cell adhesion molecule (NCAM) at virtually all gonocyte-Sertoli cell (and Sertoli cell-Sertoli cell) boundaries and found that incubation of cocultures in the continuous presence of NCAM antibodies caused release of essentially all gonocytes (but not Sertoli cells) from the monolayer. We also found, in (3) above, that gonocyte-Sertoli cell adhesion was very susceptible to phospholipase C in cocultures isolated from newborns and maintained in vitro for 2 hours or 1 day but not in cultures maintained for 3 days. Moreover, cells isolated from pups 5 days old were as resistant to enzyme treatment at 2 hours postplating as were cultures from newborns after 3 days in vitro. Thus, the way in which gonocytes adhere to Sertoli cells appears to change during the immediate postnatal period, as reflected by the observed change in phopholipase sensitivity, perhaps indicating production of a phospholipase C-resistant NCAM isoform by several days after birth. These data constitute new information on the way in which postnatal gonocytes adhere to Sertoli cells and provide a basis for future work in our ongoing exploration of germ cell development in the neonatal rat testis.
在大鼠睾丸的新生儿发育过程中,生殖母细胞恢复有丝分裂并表现出重新的运动能力,向基膜迁移,当这些细胞与支持细胞共培养时,这两个事件会在体外发生。然而,尽管大量证据表明生殖母细胞的发育依赖于支持细胞,但除了我们之前观察到它们通过缝隙连接进行通讯并彼此紧密粘附外,对于这些细胞类型如何相互作用知之甚少。在本研究中,我们采用了几种方法来研究生殖母细胞在体外粘附于支持细胞的机制。首先,我们通过以下方式总体表征这种粘附:(1) 在降低的Ca2+浓度下确定其对短暂胰蛋白酶处理的敏感性,(2) 评估生殖母细胞在降低温度下粘附于支持细胞的能力,以及(3) 检查磷脂酶C处理对附着于支持细胞单层的生殖母细胞数量的影响。由于研究结果表明涉及一种非钙粘蛋白机制,我们使用免疫荧光法在几乎所有生殖母细胞 - 支持细胞(以及支持细胞 - 支持细胞)边界处鉴定神经细胞粘附分子(NCAM)的存在,并发现将共培养物在NCAM抗体持续存在的情况下孵育会导致基本上所有生殖母细胞(但不包括支持细胞)从单层中释放出来。我们还在上述(3)中发现,从新生儿分离并在体外维持2小时或1天的共培养物中,生殖母细胞 - 支持细胞粘附对磷脂酶C非常敏感,但在维持3天的培养物中则不然。此外,从5日龄幼崽分离的细胞在接种后2小时对酶处理的抗性与体外培养3天的新生儿培养物相同。因此,生殖母细胞粘附于支持细胞的方式在出生后立即的时期似乎会发生变化,这通过观察到的磷脂酶敏感性变化得以反映,这可能表明出生几天后产生了一种对磷脂酶C有抗性的NCAM异构体。这些数据构成了关于出生后生殖母细胞如何粘附于支持细胞的新信息,并为我们正在进行的对新生大鼠睾丸生殖细胞发育的探索中的未来工作提供了基础。