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大鼠肝细胞胰岛素样生长因子I及其结合蛋白:生长激素在体内外的作用

Rat hepatocyte insulin-like growth factor I and binding protein: effect of growth hormone in vitro and in vivo.

作者信息

Scott C D, Martin J L, Baxter R C

出版信息

Endocrinology. 1985 Mar;116(3):1102-7. doi: 10.1210/endo-116-3-1102.

Abstract

This study examines the regulation of insulin-like growth factor I (IGF I) and binding protein (BP) release by adult rat hepatocytes in primary culture. Increasing the density of plating of cells had a marked positive effect on the IGF I production rate per mg cell protein, with the highest rate, approximately 4 pmol/mg cell protein X 24 h, seen at densities of 1 X 10(5) cells/cm2 or higher. Cycloheximide (15 micrograms/ml) inhibited both IGF I and BP production by more than 90%, while actinomycin D (0.1 microgram/ml) caused less marked, but still significant, inhibition. Over the insulin range 30 pM-300 nM there was a 45% increase in IGF I production, but no effect on BP production. Bovine GH stimulated production of both peptides, significant effects (up to 50% stimulation) being seen at concentrations from 20-500 ng/ml. Cells from hypophysectomized rats, with serum IGF I and GH levels reduced more than 90% from normal, had IGF I and BP production rates only 7% of normal, measured after 48 h in culture. In vivo replacement with rat GH, 150 micrograms/day for 5 days by osmotic minipump, significantly restored the production of both peptides by hepatocytes. Cells isolated from rats bearing the GH-secreting tumor, MtT/W15, had IGF I and BP production rates approximately twice as high as normal. A significant stimulatory effect of bovine GH (200 ng/ml) in vitro was seen on cells from normal and hypophysectomized, GH-replaced rats, but not from unreplaced hypophysectomized, or tumor-bearing rats. The results in hypophysectomized, animals are consistent with known changes in hepatic GH receptors, while the lack of GH responsiveness in tumor-bearing rats indicates a persistence of maximal stimulation in culture. The reflection of in vivo GH status by hepatocytes cultured for 48 h suggests that messenger RNA turnover for IGF I and BP must be slow. The close parallel in the regulation of the two peptides under most conditions might be indicative of coordinated synthesis.

摘要

本研究检测了原代培养的成年大鼠肝细胞对胰岛素样生长因子I(IGF I)及结合蛋白(BP)释放的调节作用。增加细胞接种密度对每毫克细胞蛋白的IGF I产生率有显著的正向影响,在细胞密度为1×10⁵个细胞/cm²或更高时,产生率最高,约为4 pmol/毫克细胞蛋白×24小时。放线菌酮(15微克/毫升)抑制IGF I和BP的产生超过90%,而放线菌素D(0.1微克/毫升)的抑制作用虽不那么显著,但仍很明显。在胰岛素浓度范围为30 pM - 300 nM时,IGF I的产生增加了45%,但对BP的产生无影响。牛生长激素(GH)刺激这两种肽的产生,在浓度为20 - 500 ng/ml时可见显著作用(刺激高达50%)。来自垂体切除大鼠的细胞,其血清IGF I和GH水平比正常水平降低了90%以上,在培养48小时后,其IGF I和BP产生率仅为正常水平的7%。通过渗透微型泵以每天150微克的剂量给垂体切除大鼠进行5天的大鼠GH体内替代,可显著恢复肝细胞对这两种肽的产生。从分泌GH的肿瘤MtT/W15大鼠分离的细胞,其IGF I和BP产生率约为正常水平的两倍。在体外,牛GH(200 ng/ml)对正常、垂体切除且经GH替代的大鼠的细胞有显著刺激作用,但对未替代的垂体切除大鼠或荷瘤大鼠的细胞无此作用。垂体切除动物的结果与肝脏GH受体的已知变化一致,而荷瘤大鼠缺乏GH反应性表明在培养中存在最大刺激的持续性。培养48小时的肝细胞对体内GH状态的反映表明,IGF I和BP的信使核糖核酸周转率一定很慢。在大多数情况下,这两种肽调节的密切平行可能表明它们是协同合成的。

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