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佛波酯、环磷酸腺苷和雌二醇-17β依赖性途径对大鼠颗粒细胞有丝分裂的调控

Control of rat granulosa cell mitosis by phorbol ester-, cyclic AMP-, and estradiol-17 beta-dependent pathways.

作者信息

Peluso J J, Pappalardo A, White B A

机构信息

Department of Obstetrics and Gynecology, University of Connecticut Health Center, Farmington 06032.

出版信息

Biol Reprod. 1993 Aug;49(2):416-22. doi: 10.1095/biolreprod49.2.416.

DOI:10.1095/biolreprod49.2.416
PMID:8396996
Abstract

The present studies examined the effect of 8-bromo-cAMP (8-Br-cAMP), phorbol ester (TPA), and estradiol-17 beta (E2) on the capacity of rat granulosa cells (GC) to undergo mitosis. In the first series of experiments, GC were either maintained within immature rat ovaries in perifusion culture or isolated and placed in tissue culture. GC were cultured for 24 h with 1) control medium, 2) 8-Br-cAMP, 3) TPA, or 4) 8-Br-cAMP plus TPA in the presence of 3H-thymidine (3H-T). In perifusion culture, 8-Br-cAMP stimulated both 3H-T incorporation (p < 0.05) and E2 secretion (p < 0.05) while TPA increased 3H-T (p < 0.05) without altering E2 secretion (p > 0.05). Simultaneous exposure to 8-Br-cAMP and TPA enhanced 3H-T incorporation and suppressed E2 as compared to 8-Br-cAMP treatment alone (p < 0.05). In tissue culture, 8-Br-cAMP did not increase 3H-T incorporation or cell number. TPA increased both 3H-T incorporation (p < 0.05) and cell number (p < 0.05), while 8-Br-cAMP suppressed both of these TPA-induced responses. In the presence of testosterone, 1) TPA's mitogenic action was also observed, 2) basal E2 secretion ranged between 30 and 35 pg/ml, 3) neither 8-Br-cAMP nor TPA stimulated E2 secretion over basal levels, and 4) Rp-cAMP, a cAMP antagonist, blocked TPA-induced cell proliferation. E2 at 250 pg/ml also blocked TPA's mitogenic action. In a second series of experiments, GC were collected from eCG-treated rats.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究检测了8-溴环磷腺苷(8-Br-cAMP)、佛波酯(TPA)和17β-雌二醇(E2)对大鼠颗粒细胞(GC)进行有丝分裂能力的影响。在第一系列实验中,GC要么在未成熟大鼠卵巢内进行灌流培养,要么分离出来置于组织培养中。GC在含有3H-胸腺嘧啶核苷(3H-T)的情况下,用以下培养基培养24小时:1)对照培养基;2)8-Br-cAMP;3)TPA;4)8-Br-cAMP加TPA。在灌流培养中,8-Br-cAMP刺激3H-T掺入(p<0.05)和E2分泌(p<0.05),而TPA增加3H-T掺入(p<0.05),但不改变E2分泌(p>0.05)。与单独使用8-Br-cAMP处理相比,同时暴露于8-Br-cAMP和TPA可增强3H-T掺入并抑制E2分泌(p<0.05)。在组织培养中,8-Br-cAMP未增加3H-T掺入或细胞数量。TPA增加3H-T掺入(p<0.05)和细胞数量(p<0.05),而8-Br-cAMP抑制这两种TPA诱导的反应。在睾酮存在的情况下:1)也观察到TPA的促有丝分裂作用;2)基础E2分泌在30至35 pg/ml之间;3)8-Br-cAMP和TPA均未刺激E2分泌超过基础水平;4)cAMP拮抗剂Rp-cAMP可阻断TPA诱导的细胞增殖。250 pg/ml的E2也可阻断TPA的促有丝分裂作用。在第二系列实验中,从经eCG处理的大鼠中收集GC。(摘要截短于250字)

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