Marchlewicz Mariola, Wiszniewska Barbara, Kurzawa Rafał, Wenda-Rózewicka Lidia
Department of Histology and Embryology, Pomeranian Medical University, Szczecin, Poland.
Folia Histochem Cytobiol. 2004;42(1):19-27. doi: 10.1007/BF02687295.
The rat epididymal epithelial cells revealed features of steroidogenic cells and released 17beta-estradiol (E2) into the culture medium. In steroidogenic cells, elements of the cytoskeleton due to their influence on organelle distribution are implicated in the regulation of steroidogenesis. In the present study, the morphology of cultured epididymal epithelial cells in light, scanning and transmission electron microscopes was evaluated. The organization of microtubules and microfilaments revealed by fluorescence microscopy, and the concentration of E2 in cultured medium were also studied. The epididymal epithelial cells were cultured in different conditions: in the medium with or without exogenous testosterone (T) and in the co-culture with Leydig cells as a source of androgens. The cells in co-culture located close to Leydig cells were rich in glycogen, PAS-positive substances and lipid droplets, in higher amount than the cells cultured with addition of exogenous testosterone. Stress fibers and microtubules of epididymal epithelial cells cultured with exogenous T and in co-culture with Leydig cells presented typical structure, and numerous granular protrusions appeared on the surface of the cells. Disorganization of microtubules and shortening of stress fibers as well as the smooth cell surface deprived of granular protrusions were observed in the epididymal epithelial cells cultured without T. Change of the cytoskeleton organization caused by the absence of androgen in culture medium resulted in an increased E2 secretion.
大鼠附睾上皮细胞表现出类固醇生成细胞的特征,并将17β-雌二醇(E2)释放到培养基中。在类固醇生成细胞中,细胞骨架成分因其对细胞器分布的影响而参与类固醇生成的调节。在本研究中,对培养的附睾上皮细胞在光学显微镜、扫描电子显微镜和透射电子显微镜下的形态进行了评估。还研究了荧光显微镜显示的微管和微丝的组织情况以及培养基中E2的浓度。附睾上皮细胞在不同条件下培养:在含有或不含有外源性睾酮(T)的培养基中,以及与作为雄激素来源的睾丸间质细胞共培养。与睾丸间质细胞共培养且靠近睾丸间质细胞的细胞富含糖原、PAS阳性物质和脂滴,其含量高于添加外源性睾酮培养的细胞。用外源性T培养以及与睾丸间质细胞共培养的附睾上皮细胞的应力纤维和微管呈现典型结构,并且细胞表面出现大量颗粒状突起。在无T培养的附睾上皮细胞中观察到微管紊乱、应力纤维缩短以及细胞表面光滑且无颗粒状突起。培养基中雄激素缺乏导致的细胞骨架组织变化导致E2分泌增加。