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雌激素和孕激素对猴催乳素合成的影响。

The effect of estrogens and progestins on monkey prolactin synthesis.

作者信息

Bethea C L

出版信息

Endocrinology. 1986 Aug;119(2):771-9. doi: 10.1210/endo-119-2-771.

Abstract

Dispersed monkey pituitary cells were cultured on extracellular matrix and in serum-free medium for up to 1 month, with medium changes every other day. The cells were treated with ethanol vehicle or 10 nM 17 beta-estradiol (E2 beta), 17 alpha-estradiol (E2 alpha), progesterone (P4), pregnenalone (P5), 17 alpha-hydroxyprogesterone (17OH P4), and E2 beta plus P4. Immunoreactive PRL (IR-PRL) levels in 48 h medium samples were first determined with a homologous human PRL RIA and then with a heterologous monkey PRL RIA. On the last day of culture, the cells were incubated with [35S]methionine for 4 h, and 35S-labeled PRL in the medium and cells was determined and compared to 4 h IR-PRL. Differences between control and treated groups in 48 h IR-PRL were greater with the heterologous monkey RIA. E2 beta, E2 alpha, and E2 beta plus P4 significantly elevated IR-PRL in 48 h medium samples an average of 73%, as determined with the monkey RIA. P4, P5, or 17OH P4 had no effect on IR-PRL in 48 h medium samples. Secreted and intracellular [35S]PRL were consistently elevated by E2 beta and E2 beta plus P4, but less consistently elevated by E2 alpha. P4, P5, or 17OH P4 had little effect on [35S]PRL in medium or cells. IR-PRL in the 4 h medium sample and cells generally paralleled [35S]PRL, although E2 alpha caused a more consistent elevation in IR-PRL than in [35S]PRL. In summary, E2 beta and E2 alpha directly stimulate PRL synthesis by monkey pituitary cells on extracellular matrix in long term serum-free culture. Nanomolar levels of progestins have little direct effect on PRL synthesis, nor does 10 nM P4 block the stimulatory effect of E2 beta.

摘要

将分散的猴垂体细胞接种于细胞外基质上,并在无血清培养基中培养长达1个月,每隔一天更换培养基。细胞用乙醇载体或10 nM的17β-雌二醇(E2β)、17α-雌二醇(E2α)、孕酮(P4)、孕烯醇酮(P5)、17α-羟孕酮(17OH P4)以及E2β加P4进行处理。首先用同源人PRL放射免疫分析法(RIA),然后用异源猴PRL RIA测定48小时培养基样本中的免疫反应性PRL(IR-PRL)水平。在培养的最后一天,将细胞与[35S]甲硫氨酸孵育4小时,测定培养基和细胞中35S标记的PRL,并与4小时的IR-PRL进行比较。用异源猴RIA检测时,对照组和处理组之间48小时IR-PRL的差异更大。用猴RIA测定,E2β、E2α以及E2β加P4使48小时培养基样本中的IR-PRL显著升高,平均升高73%。P4、P5或17OH P4对48小时培养基样本中的IR-PRL无影响。E2β以及E2β加P4使分泌型和细胞内的[35S]PRL持续升高,但E2α升高的情况不太一致。P4、P5或17OH P4对培养基或细胞中的[35S]PRL影响很小。4小时培养基样本和细胞中的IR-PRL通常与[35S]PRL平行,尽管E2α导致IR-PRL升高比[35S]PRL更一致。总之,在长期无血清培养中,E2β和E2α直接刺激猴垂体细胞在细胞外基质上合成PRL。纳摩尔水平的孕激素对PRL合成几乎没有直接影响,10 nM的P4也不阻断E2β的刺激作用。

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