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组织培养中生长激素对胎鼠胰岛中生长调节素C/胰岛素样生长因子I产生及DNA复制的调控

Growth hormone regulation of somatomedin C/insulin-like growth factor I production and DNA replication in fetal rat islets in tissue culture.

作者信息

Swenne I, Hill D J, Strain A J, Milner R D

出版信息

Diabetes. 1987 Mar;36(3):288-94. doi: 10.2337/diab.36.3.288.

Abstract

The regulation of DNA replication by growth hormone and the production of somatomedin C/insulin-like growth factor I (SM-C/IGF-I) and insulin by fetal rat islets in culture has been studied. Islets were cultured for 3 days in medium containing 2.7 or 16.7 mM glucose, various concentrations of fetal calf serum (FCS), and 100-1000 ng/ml human growth hormone (GH). DNA replication was determined by incorporation of [3H]thymidine into islet DNA; SM-C/IGF-I and insulin secreted into the medium were measured by specific radioimmunoassays. Glucose caused a twofold stimulation of islet DNA replication in medium containing greater than or equal to 1% FCS but failed to stimulate DNA replication at lower serum concentrations. In the presence of 16.7 mM glucose, GH (100-1000 ng/ml) stimulated DNA replication at all serum concentrations. In medium containing 2.7 mM glucose, GH was stimulatory only in the presence of 1% FCS. Somatomedin C/IGF-I release into the culture medium could be detected in all experimental groups. Glucose alone did not affect SM-C/IGF-I release, and in serum concentrations less than 0.1% FCS, GH also failed to increase the release of the peptide. In medium containing 1% FCS and 16.7 mM glucose, 100-1000 ng/ml GH caused a 50-100% increase in SM-C/IGF-I release into the medium. Addition of 100 ng/ml exogenous SM-C/IGF-I to medium containing 16.7 mM glucose and 0.1-1.0% FCS caused a twofold stimulation of the islet DNA replication. This effect could be abolished by the addition of an antibody to SM-C/IGF-I.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了生长激素对DNA复制的调节以及培养的胎鼠胰岛中生长调节素C/胰岛素样生长因子I(SM-C/IGF-I)和胰岛素的产生。胰岛在含有2.7或16.7 mM葡萄糖、不同浓度胎牛血清(FCS)以及100 - 1000 ng/ml人生长激素(GH)的培养基中培养3天。通过将[3H]胸腺嘧啶掺入胰岛DNA来测定DNA复制;通过特异性放射免疫测定法测量分泌到培养基中的SM-C/IGF-I和胰岛素。在含有大于或等于1% FCS的培养基中,葡萄糖使胰岛DNA复制增加两倍,但在较低血清浓度下未能刺激DNA复制。在存在16.7 mM葡萄糖的情况下,GH(100 - 1000 ng/ml)在所有血清浓度下均刺激DNA复制。在含有2.7 mM葡萄糖的培养基中,GH仅在存在1% FCS时具有刺激作用。在所有实验组中均可检测到生长调节素C/IGF-I释放到培养基中。单独的葡萄糖不影响SM-C/IGF-I释放,并且在血清浓度低于0.1% FCS时,GH也未能增加该肽的释放。在含有1% FCS和16.7 mM葡萄糖的培养基中,100 - 1000 ng/ml GH使释放到培养基中的SM-C/IGF-I增加50 - 100%。向含有16.7 mM葡萄糖和0.1 - 1.0% FCS的培养基中添加100 ng/ml外源性SM-C/IGF-I可使胰岛DNA复制增加两倍。添加抗SM-C/IGF-I抗体可消除这种作用。(摘要截短于250字)

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