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[黄体化过程中颗粒细胞膜流动性的变化]

[Changes in the plasma membrane fluidity of granulosa cells during the process of luteinization].

作者信息

Negishi H

机构信息

Department of Obstetrics and Gynecology, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Hokkaido Igaku Zasshi. 1991 Nov;66(6):739-48.

PMID:1783364
Abstract

To elucidate the membrane fluidity of granulosa cells in luteinization process, porcine granulosa cells (GCs) were cultured in the serum free medium under the stimulation of human chorionic gonadotropin (hCG). Their cell membrane anisotropy, membrane lipid composition and progesterone synthesis were measured. The GCs plasma membrane anisotropy, which is reverse to fluidity, was measured with the steady-state spectrofluorometer using a hydrophobic fluorescent probe 1, 6-diphenyl-1, 3, 5-hexatriene (DPH). Since the membrane fluidity is generally affected by concentrations of cholesterol and phospholipids, phospholipid composition and the degree of unsaturation of acyl chain, concentrations of unesterified cholesterol and phospholipids, and phospholipid composition in the plasma membranes of GCs were determined. The results obtained were as follows. 1) The value of the anisotropy (membrane fluidity) of the GCs stimulated by hCG decreased (increased) significantly as compared to that without hCG addition. 2) The concentration of cholesterol in plasma membrane fraction decreased significantly by hCG stimulation. 3) In contrast, the concentration and composition of phospholipids showed no significant changes. 4) Progesterone concentration in culture medium was significantly increased by hCG stimulation at 30 mlU/ml and 300 mlU/ml throughout the time course of this study, compared with control. These results indicate the increase of membrane fluidity of the GCs luteinization induced by hCG is due to a decrease of cholesterol/phospholipids ratio. Because transfer of cholesterol into culture medium was not observed, it seems that the cholesterol of the GCs plasma membranes was utilized for progesterone synthesis at least in the serum free medium (GIT medium) during the process of luteinization.

摘要

为阐明黄体化过程中颗粒细胞的膜流动性,将猪颗粒细胞(GCs)在无血清培养基中培养,并用人绒毛膜促性腺激素(hCG)刺激。测定了它们的细胞膜各向异性、膜脂组成和孕酮合成。使用疏水性荧光探针1,6-二苯基-1,3,5-己三烯(DPH),通过稳态荧光分光光度计测量与流动性相反的GCs质膜各向异性。由于膜流动性通常受胆固醇和磷脂浓度、磷脂组成以及酰基链不饱和度的影响,因此测定了GCs质膜中未酯化胆固醇和磷脂的浓度以及磷脂组成。得到的结果如下:1)与未添加hCG相比,hCG刺激的GCs的各向异性值(膜流动性)显著降低(增加)。2)hCG刺激使质膜部分的胆固醇浓度显著降低。3)相反,磷脂的浓度和组成没有显著变化。4)在本研究的整个时间过程中,与对照相比,30 mIU/ml和300 mIU/ml的hCG刺激使培养基中的孕酮浓度显著增加。这些结果表明,hCG诱导的GCs黄体化过程中膜流动性的增加是由于胆固醇/磷脂比值的降低。由于未观察到胆固醇向培养基中的转移,似乎在黄体化过程中,至少在无血清培养基(GIT培养基)中,GCs质膜中的胆固醇被用于孕酮合成。

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