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用于激素分泌调控研究的大鼠垂体前叶细胞的酶解及短期培养

Enzymatic dissociation and short-term culture of isolated rat anterior pituitary cells for studies on the control of hormone secretion.

作者信息

Nakano H, Fawcett C P, McCann S M

出版信息

Endocrinology. 1976 Feb;98(2):278-88. doi: 10.1210/endo-98-2-278.

Abstract

A convenient procedure has been developed for preparing a suspension of isolated rat anterior pituitary cells which retains responsiveness to secretagogues. Rat anterior pituitaries were dispersed with collagenase and hyaluronidase followed by mechanical dispersion by means of a Pasteur pipette. Immediately after dispersion, the cells showed only slight responses to secretagogues, whereas after short-term culture (20-22 h) in the presence of sera, the cells recovered their ability to respond to synthetic LH-releasing hormone (LHRH) and synthetic thyrotropin-releasing hormone (TRH). During a 3-h incubation, cells prepared from pituitaries of male rats released LH and FSH, or TSH and prolactin (PRL) in amounts directly related to the dose of synthetic LHRH or TRH, respectively. The minimum effective concentrations of hypophysiotropic hormones lay between 10(-10) and 10(-9)M, although it was observed that cells originating from female rats usually gave quicker and larger responses to LHRH. No significant net increase in the total hormonal content (cells + medium) of radioimmunoassayable LH or FSH in response to LHRH, or of TSH or PRL in response to TRH, was observed during the 3-h incubation period. The cells released significant amounts of PRL, TSH, and to a lesser extent, LH, in response to 1-5 X 10-3M N6,O2'-dibutyryl cyclic AMP, accompanied by remarkable elevation in total content (cells + medium) of PRL and TSH but not of LH. The response of the cells to theophylline or high [K+] was similar to that usually observed in previous hemipituitary experiments. These results demonstrate the viability of this in vitro cell system and its suitability for further study of the regulation of the secretion of pituitary hormones.

摘要

已开发出一种简便的方法来制备分离的大鼠垂体前叶细胞悬液,该悬液能保持对促分泌素的反应性。用胶原酶和透明质酸酶分散大鼠垂体前叶,然后用巴斯德吸管进行机械分散。分散后立即,细胞对促分泌素仅表现出轻微反应,而在有血清存在的短期培养(20 - 22小时)后,细胞恢复了对合成促黄体生成素释放激素(LHRH)和合成促甲状腺激素释放激素(TRH)的反应能力。在3小时的孵育过程中,从雄性大鼠垂体制备的细胞分别释放促黄体生成素(LH)和促卵泡生成素(FSH),或促甲状腺激素(TSH)和催乳素(PRL),其释放量与合成LHRH或TRH的剂量直接相关。促垂体激素的最小有效浓度在10^(-10)至10^(-9)M之间,不过观察到来自雌性大鼠的细胞通常对LHRH反应更快且更大。在3小时的孵育期内,未观察到放射性免疫分析可检测的LH或FSH的总激素含量(细胞 + 培养基)因LHRH刺激而有显著净增加,或TSH或PRL因TRH刺激而有显著净增加。细胞对1 - 5×10^(-3)M N6,O2'-二丁酰环磷腺苷(cAMP)有反应,释放大量PRL、TSH,以及较少程度的LH,同时PRL和TSH的总含量(细胞 + 培养基)显著升高,但LH没有。细胞对茶碱或高钾的反应与先前半垂体实验中通常观察到的相似。这些结果证明了该体外细胞系统的活力及其对进一步研究垂体激素分泌调节的适用性。

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