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Angiotensin II induces apoptosis in human mural granulosa-lutein cells, but not in cumulus cells.

机译:血管紧张素II诱导人壁颗粒-叶黄素细胞凋亡,但不诱导卵丘细胞凋亡。

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OBJECTIVE: To test whether angiotensin II (AngII) could modulate apoptosis of human granulosa-lutein (GL) cells from gonadotropin-stimulated follicles. DESIGN: In vitro assays on mural and cumulus granulosa cells. SETTING: University laboratory and private IVF practice. PATIENT(S): One hundred six consecutive women undergoing 113 IVF cycles. INTERVENTION(S): Purified human GL mural or cumulus cells were cultured in serum-free media in the presence or absence of AngII with or without the AngII receptor blockers saralasin and CGP42112A. MAIN OUTCOME MEASURE(S): Detection of apoptosis using a fluorescent in situ marker for activated caspases. RESULT(S): Mural cells had approximately eightfold the amount of apoptosis compared with cumulus cells (average 0.23 vs. <0.03, respectively). With mural cells, AngII increased GL cell apoptosis versus untreated control samples (AngII 10(-)11 mol/L +6.5%; AngII 10(-9) mol/L +13.3%, and AngII 10(-7) mol/L +11.3%), an effect which was blocked by concurrent incubation with AngII receptor blockers. The AngII receptor blockers produced a significant decrease of apoptosis compared with control cultures (saralasin: 19.4%; CGP42112A: 28.9%). Neither AngII nor blockers had effect on cumulus cells. CONCLUSION(S): Preovulatory concentrations of AngII, most likely via AT2 receptors, increase apoptosis of cultured mural GL cells but have no effect on cumulus cells. Granulosa cells appear to be differentially regulated by AngII.
机译:目的:检测血管紧张素Ⅱ(AngⅡ)是否能调节促性腺激素刺激的卵泡中人颗粒-叶黄素(GL)细胞的凋亡。设计:壁和颗粒细胞的体外测定。地点:大学实验室和私人试管婴儿诊所。患者:一百零六名连续113个试管婴儿的妇女。干预:在有或没有AngII的情况下,在有或没有AngII受体阻断剂saralasin和CGP42112A的无血清培养基中培养纯化的人GL壁或卵丘细胞。主要观察指标:使用荧光原位标记检测激活的胱天蛋白酶的凋亡。结果:壁细胞的凋亡量是卵丘细胞的八倍(分别为0.23 vs. <0.03)。与未处理的对照样品相比,壁画细胞能使AngII增加GL细胞凋亡(AngII 10(-)11 mol / L + 6.5%; AngII 10(-9)mol / L + 13.3%,AngII 10(-7)mol / L + 11.3%),此效应可通过与AngII受体阻滞剂同时孵育而被阻断。与对照培养物相比,AngII受体阻滞剂产生了显着的凋亡降低(撒拉辛:19.4%; CGP42112A:28.9%)。 AngII和阻滞剂都没有影响卵丘细胞。结论:排卵前的AngII浓度很可能通过AT2受体增加,可增加培养的壁膜GL细胞的凋亡,但对卵丘细胞没有影响。颗粒细胞似乎受到AngII的差异调节。

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