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共培养中卵巢颗粒细胞与卵泡膜细胞的相互作用会影响细胞质微管组织吗?

Does ovarian granulosa and theca cell interaction in co-culture affect the cytoplasmic microtubule organization?

作者信息

Gregoraszczuk E, Stoklosowa S, Duda M, Slomczynska M

机构信息

Department of Animal Physiology, Jagiellonian University, Krakow, Poland.

出版信息

Cytobios. 1996;88(354):133-40.

PMID:9281812
Abstract

Theca (T) cells modulate steroid secretion by granulosa (G) cells in vitro. This investigation was undertaken to see whether the cytoskeleton is involved in this process. Monocultures of G cells alone, T cells alone and GT co-cultures were viewed by light microscopy. Microtubules were visualized using monoclonal Ab against tubulin. The specificity of the Ab was checked by Western blotting. One group of cells was treated with colchicine, a microtubule disrupting drug, to show its influence on oestradiol secretion by cultured cells. Microtubule arrangement was monitored using a fluorescence microscope. In monoculture of G cells a diffuse pattern of immunocytochemical staining of tubulin was noted while in T cells cultured alone the microtubule were arranged in a network of delicate fibres. In co-culture the microtubule arrangement changed in G cells and became very fine and less numerous than in theca fibres. Oestradiol secretion by colchicine-treated cultures different from control secretions. The E2 secretion declined in cultures of G cells (48.9 pg/10(5) cells in control vs 19.4 pg/10(5) cells in colchicine cells), and in T cells cultures alone (490 pg i n control vs 171 pg/10(5) cells in colchicine treated cells) while in co-culture a dose-dependent increase of this steroid was detected after the addition of colchicine (2,008 pg vs 1,269 pg/10(5) cells in control). It is conceivable that microtubules affect transport of androgens from their production site in T cells to G cells where this substrate is aromatized resulting in increased preovulatory oestradiol secretion.

摘要

卵泡膜(T)细胞在体外可调节颗粒(G)细胞的类固醇分泌。本研究旨在探讨细胞骨架是否参与这一过程。通过光学显微镜观察单独培养的G细胞、单独培养的T细胞以及GT共培养物。使用抗微管蛋白的单克隆抗体使微管可视化。通过蛋白质免疫印迹法检测抗体的特异性。一组细胞用秋水仙碱(一种破坏微管的药物)处理,以显示其对培养细胞雌二醇分泌的影响。使用荧光显微镜监测微管排列。在G细胞的单培养中,观察到微管蛋白的免疫细胞化学染色呈弥散模式,而在单独培养的T细胞中,微管排列成精细的纤维网络。在共培养中,G细胞中的微管排列发生变化,变得非常纤细,且数量比卵泡膜纤维中的少。秋水仙碱处理的培养物的雌二醇分泌与对照分泌不同。在G细胞培养物中,E2分泌下降(对照中为48.9 pg/10⁵细胞,秋水仙碱处理的细胞中为19.4 pg/10⁵细胞),在单独的T细胞培养物中也下降(对照中为490 pg,秋水仙碱处理的细胞中为171 pg/10⁵细胞),而在共培养中,添加秋水仙碱后检测到这种类固醇呈剂量依赖性增加(对照中为1269 pg/10⁵细胞,添加后为2008 pg/10⁵细胞)。可以想象,微管影响雄激素从其在T细胞中的产生部位向G细胞的转运,在G细胞中该底物被芳香化,导致排卵前雌二醇分泌增加。

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