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转化生长因子β1对小鼠成骨细胞MC3T3-E1细胞中HSP47基因的转录激活作用

Transcriptional activation of the mouse HSP47 gene in mouse osteoblast MC3T3-E1 cells by TGF-beta 1.

作者信息

Yamamura I, Hirata H, Hosokawa N, Nagata K

机构信息

Department of Oral and Maxillofacial Surgery, Faculty of Medicine, Kyoto University, Japan.

出版信息

Biochem Biophys Res Commun. 1998 Mar 6;244(1):68-74. doi: 10.1006/bbrc.1998.8216.

Abstract

HSP47 is a 47-kDa collagen-binding heat shock protein, the expression of which is always correlated with that of collagens in various cell lines. We examined the effects of TGF-beta 1, which is reported to induce the collagen genes, on the expression of HSP47 in mouse osteoblast MC3T3-E1 cells. Treatment of the cells with 5 ng/ml TGF-beta 1 for 24 h increased the level of HSP47 mRNA three-fold. Dose-dependent induction by TGF-beta 1 was observed for both HSP47 mRNA and collagen alpha 1 (I) mRNA, and actinomycin D inhibited this increase of HSP47 mRNA. To elucidate the TGF-beta 1 responsive element(s) in the mouse HSP47 gene, we generated a series of 5'-deletion promoters fused to luciferase reporter constructs. Transient transfection assays showed that TGF-beta 1 induced 4-6 fold the promoter activity of a region approximately -5.5 kbp upstream of the HSP47 gene. Two upstream regions, -3.9 to -2.7 kbp and -280 to -50 bp were shown to be involved in the activation in response to TGF-beta 1 treatment.

摘要

热休克蛋白47(HSP47)是一种47千道尔顿的胶原结合热休克蛋白,其表达在各种细胞系中总是与胶原蛋白的表达相关。我们研究了据报道可诱导胶原基因的转化生长因子β1(TGF-β1)对小鼠成骨细胞MC3T3-E1细胞中HSP47表达的影响。用5纳克/毫升TGF-β1处理细胞24小时,使HSP47 mRNA水平增加了三倍。对于HSP47 mRNA和胶原α1(I)mRNA,均观察到TGF-β1的剂量依赖性诱导,且放线菌素D抑制了HSP47 mRNA的这种增加。为了阐明小鼠HSP47基因中的TGF-β1反应元件,我们构建了一系列与荧光素酶报告基因构建体融合的5'-缺失启动子。瞬时转染实验表明,TGF-β1可使HSP47基因上游约-5.5千碱基对区域的启动子活性诱导4至6倍。两个上游区域,即-3.9至-2.7千碱基对和-280至-50碱基对,被证明参与了对TGF-β1处理的激活反应。

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