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多囊卵巢综合征患者卵巢中Fas和Fas配体的免疫定位:与细胞凋亡的关系

Immunolocalization of Fas and Fas ligand in the ovaries of women with polycystic ovary syndrome: relationship to apoptosis.

作者信息

Cataldo N A, Dumesic D A, Goldsmith P C, Jaffe R B

机构信息

Center for Reproductive Sciences, Department of Obstetrics, Gynecology and Reproductive Sciences, University of California San Francisco, San Francisco, CA 94143-0556, USA.

出版信息

Hum Reprod. 2000 Sep;15(9):1889-97. doi: 10.1093/humrep/15.9.1889.

Abstract

Both Fas (APO-1, CD95), an apoptosis-inducing receptor, and its ligand, Fas ligand (FasL, CD95L), have been localized to the ovary. Granulosa cell apoptosis occurs in antral follicular atresia. In polycystic ovary syndrome (PCOS), antral follicles accumulate with some atretic features. The ovarian expression of Fas and FasL was examined in PCOS by immunohistochemistry and correlated with immunodetection of apoptotic cells. Fas immunostaining was present in pre-antral follicle oocytes, some primary and secondary pre-antral follicle granulosa cells, and both granulosa and theca of antral follicles. Thecal staining persisted with advancing atresia, while granulosa staining declined. In antral follicles, abundant Fas-positive cells co-localized with scattered nuclei immunopositive for apoptosis. Ovarian vascular myocytes were strongly Fas-immunopositive. FasL immunostaining was present in pre-antral follicles in oocytes and variably in granulosa. In antral follicles, granulosa and thecal FasL staining increased with advancing atresia. Normal control ovaries showed follicular Fas and FasL staining patterns similar to those in PCOS, but vascular staining was less prominent. In one healthy follicle, Fas immunostaining was seen in the oocyte and weakly in mural granulosa and theca interna. The results suggest that in PCOS, an alteration in Fas-mediated apoptosis, does not cause abnormal folliculogenesis, but may promote ovarian vascular remodelling.

摘要

凋亡诱导受体Fas(APO-1,CD95)及其配体Fas配体(FasL,CD95L)均已定位到卵巢。颗粒细胞凋亡发生在窦状卵泡闭锁过程中。在多囊卵巢综合征(PCOS)中,窦状卵泡会累积并伴有一些闭锁特征。通过免疫组织化学检测了PCOS患者卵巢中Fas和FasL的表达,并将其与凋亡细胞的免疫检测结果进行关联。Fas免疫染色出现在窦前卵泡卵母细胞、一些初级和次级窦前卵泡颗粒细胞以及窦状卵泡的颗粒细胞和卵泡膜细胞中。随着闭锁程度加重,卵泡膜细胞染色持续存在,而颗粒细胞染色减少。在窦状卵泡中,大量Fas阳性细胞与散在的凋亡免疫阳性细胞核共定位。卵巢血管平滑肌细胞Fas免疫阳性强烈。FasL免疫染色出现在窦前卵泡的卵母细胞中,颗粒细胞中染色情况不一。在窦状卵泡中,随着闭锁程度加重,颗粒细胞和卵泡膜细胞的FasL染色增加。正常对照卵巢的卵泡Fas和FasL染色模式与PCOS患者相似,但血管染色不那么明显。在一个健康卵泡中,卵母细胞可见Fas免疫染色,壁层颗粒细胞和卵泡内膜细胞中染色较弱。结果表明,在PCOS中,Fas介导的凋亡改变不会导致异常卵泡发生,但可能促进卵巢血管重塑。

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