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雌二醇对垂体片段中促性腺激素基因转录的不同影响。

Divergent effects of estradiol on gonadotropin gene transcription in pituitary fragments.

作者信息

Shupnik M A, Gharib S D, Chin W W

机构信息

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.

出版信息

Mol Endocrinol. 1989 Mar;3(3):474-80. doi: 10.1210/mend-3-3-474.

DOI:10.1210/mend-3-3-474
PMID:2501667
Abstract

Our previous work demonstrated that in vivo estradiol (E2) administration to ovariectomized rats suppressed the transcription of the LH subunit genes within 4 h. To determine whether these effects were mediated directly at the level of the gonadotrope, the transcription rates of the LH beta, FSH beta, and alpha-subunits were measured in short term cultures of pituitary fragments from female rats in various physiological states. In each in vitro experiment, fragments from matched sets of hemipituitaries were used for control and treatment (10(-8)ME2) groups. In pituitaries from ovariectomized animals, treated in vitro with or without E2, there was no significant effect of 2 h or 6 h of E2 on FSH beta or alpha-subunit gene transcription, but a consistent 2- to 3-fold stimulation of LH beta mRNA synthesis. In pituitaries from intact randomly cycling rats, E2 in culture had no effect on the transcription rate of alpha-subunit, FSH beta, or TSH beta genes, but stimulated LH beta and PRL transcription 2-fold. Thyroid hormone treatment specifically suppressed alpha-subunit (38% of control) and TSH beta (17% of control) mRNA synthesis, indicating that the culture system is responding in an appropriate physiological manner and that decreases in transcription can be easily and accurately measured with this system. Basal and E2-treated transcription rates for each gonadotropin subunit gene were measured as a function of stage of the estrous cycle. Basal transcription of the alpha-subunit gene did not vary significantly throughout the cycle and did not respond to E2 treatment in vitro.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们之前的研究表明,给去卵巢大鼠体内注射雌二醇(E2)可在4小时内抑制促黄体生成素(LH)亚基基因的转录。为了确定这些作用是否直接在促性腺激素细胞水平介导,我们在处于不同生理状态的雌性大鼠垂体片段的短期培养物中测量了LHβ、FSHβ和α亚基的转录率。在每个体外实验中,来自配对半垂体的片段用于对照组和处理组(10^(-8)M E2)。在去卵巢动物的垂体中,无论体外是否用E2处理,2小时或6小时的E2对FSHβ或α亚基基因转录均无显著影响,但对LHβ mRNA合成有持续2至3倍的刺激作用。在完整的随机发情大鼠的垂体中,培养中的E2对α亚基、FSHβ或TSHβ基因的转录率没有影响,但刺激LHβ和PRL转录2倍。甲状腺激素处理特异性抑制α亚基(对照的38%)和TSHβ(对照的17%)mRNA合成,表明培养系统以适当的生理方式做出反应,并且使用该系统可以轻松准确地测量转录的降低。每个促性腺激素亚基基因的基础转录率和E2处理后的转录率作为发情周期阶段的函数进行测量。α亚基基因的基础转录在整个周期中没有显著变化,并且在体外对E2处理没有反应。(摘要截断于250字)

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Mol Endocrinol. 1989 Mar;3(3):474-80. doi: 10.1210/mend-3-3-474.
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