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胰岛素样生长因子-I和胰岛素样生长因子-II在小鼠成骨细胞中诱导c-fos表达。

Insulin-like growth factor-I and insulin-like growth factor-II induce c-fos in mouse osteoblastic cells.

作者信息

Merriman H L, La Tour D, Linkhart T A, Mohan S, Baylink D J, Strong D D

机构信息

Department of Biochemistry, Loma Linda University, California.

出版信息

Calcif Tissue Int. 1990 Apr;46(4):258-62. doi: 10.1007/BF02555005.

Abstract

We investigated the expression of c-fos in mouse osteoblast-like cultures treated with insulin-like growth factor (IGF)-I and IGF-II. The IGFs are present in bone, are produced by osteoblast-like cells in culture, and stimulate osteoblast cell proliferation. Quiescent, subconfluent cultures of the clonal osteoblast-like mouse calvarial cell line, MC3T3-E1, were treated with 10 ng/ml of IGF-I or IGF-II. RNA was extracted at 0, 15, 30, 60, 120 and 240 minutes, and c-fos messenger RNA (mRNA) was analyzed on Northern blots. Both IGFs transiently increased c-fos mRNA levels 25-28 fold at 15-30 min. To determine if c-fos induction was unique to the MC3T3-E1 cell line, effects of IGF-1 and IGF-II (3 ng/ml) were also tested in quiescent, serum-free primary mouse calvarial cells. Levels of c-fos mRNA were increased at 15 and 30 minutes (40-fold with IGF-I and 5-fold with IGF-II). These results indicate that IGF-I and IGF-II caused a rapid and transient induction of c-fos mRNA in murine osteoblasts.

摘要

我们研究了胰岛素样生长因子(IGF)-I和IGF-II处理的小鼠成骨细胞样培养物中c-fos的表达。IGF存在于骨中,由培养的成骨细胞样细胞产生,并刺激成骨细胞增殖。用10 ng/ml的IGF-I或IGF-II处理克隆的小鼠颅骨成骨细胞样细胞系MC3T3-E1的静止、亚汇合培养物。在0、15、30、60、120和240分钟提取RNA,并在Northern印迹上分析c-fos信使核糖核酸(mRNA)。两种IGF在15 - 30分钟时均使c-fos mRNA水平瞬时增加25 - 28倍。为了确定c-fos诱导是否是MC3T3-E1细胞系特有的,还在静止的无血清原代小鼠颅骨细胞中测试了IGF-1和IGF-II(3 ng/ml)的作用。c-fos mRNA水平在第15和30分钟时升高(IGF-I升高40倍,IGF-II升高5倍)。这些结果表明,IGF-I和IGF-II在小鼠成骨细胞中引起c-fos mRNA的快速和瞬时诱导。

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