Bilinska B
Department of Animal Physiology, Jagiellonian University, Krakow, Poland.
Eur J Histochem. 1993;37(1):27-31.
Since it is known that Sertoli cells modulate steroid production by Leydig cells in vitro, an effort was made to see whether the cytoskeleton is involved in this process. Cocultures of Leydig and Sertoli cells were examined in the light microscope equipped with Nomarski optics. To distinguish Leydig cells from Sertoli cells, a histochemical test for delta 5, 3 beta-hydroxysteroid dehydrogenase activity was performed. To visualize microfilaments (MFs), staining with rhodamine labeled phalloidin was used. In coculture, changes of Leydig cell shape towards regular and rounded as well as an increase of androgen production were observed. Concurrently, changes in the microfilament organization were seen. Stress fibers visible in Leydig cells cultured alone, were dispersed or even disappeared when grown in coculture. This effect was strengthened in the presence of FSH in the culture medium, which was not the case in monoculture of Leydig cells. Results are discussed with respect to a possible stimulation of Leydig cell function by Sertoli cells in vitro.
由于已知支持细胞在体外可调节间质细胞的类固醇生成,因此我们试图探究细胞骨架是否参与这一过程。利用配备了诺马斯基光学系统的光学显微镜对间质细胞和支持细胞的共培养物进行检查。为了区分间质细胞和支持细胞,我们进行了5,3β - 羟类固醇脱氢酶活性的组织化学检测。为了观察微丝(MFs),我们使用罗丹明标记的鬼笔环肽进行染色。在共培养中,观察到间质细胞形状变为规则且圆润,同时雄激素生成增加。与此同时,微丝组织也发生了变化。单独培养的间质细胞中可见的应力纤维,在共培养时会分散甚至消失。在培养基中存在促卵泡激素(FSH)时,这种效应会增强,而在间质细胞的单培养中则不会出现这种情况。本文针对支持细胞在体外可能对间质细胞功能产生的刺激作用进行了讨论。