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电离辐射对培养的大鼠心脏细胞基因表达的影响。

Effects of ionizing radiation on gene expression in cultured rat heart cells.

作者信息

Boerma M, Bart C I, Wondergem J

机构信息

LUMC, Department of Clinical Oncology, K1P, Albinusdreef 2, 2333 ZA Leiden, The Netherlands.

出版信息

Int J Radiat Biol. 2002 Mar;78(3):219-25. doi: 10.1080/09553000110094797.

Abstract

PURPOSE

To determine the in vitro effect of ionizing radiation on TGF-beta1, FGF-2, IL-1beta, atrial natriuretic peptide (ANP) and procollagen types I and III gene expression in three different cell types of rat heart.

MATERIALS AND METHODS

Primary cell cultures of myocytes and fibroblasts and cultures of a rat heart endothelial cell line (RHEC) were irradiated with single doses of 2.0, 8.5 or 15 Gy. At different time-points after irradiation (4-336 h), gene expression was analysed using a competitive PCR technique.

RESULTS

Irradiation of cultured rat heart cells may lead to temporary changes in expression of the genes studied. Analysis of the radiation response of cultured myocytes, cardiac fibroblasts and rat heart endothelial cells reveals different responses with regard to (1) the dose necessary to evoke changes in mRNA expression, (2) the level of and (3) the duration of the 'induced' response. The changes observed were small and between parallel experiments the onset and time-course of the induced gene expression varied between 4 and 48 h. The average expression of TGF-beta1 mRNA between 4 and 48 h was significantly elevated in endothelial cells after a dose of 2.0 Gy, in fibroblasts after a dose of 8.5 Gy and in myocytes after a dose of 15 Gy. Down-regulation of TGF-beta1 mRNA in myocytes was observed after a dose of 8.5 Gy. FGF-2 and procollagen type-I mRNAs were significantly elevated in fibroblasts after a dose of 2.0 Gy. For all three cell types, no effect of dose on the timing or size of the gene expression was observed.

CONCLUSIONS

Although irradiation of cultured heart cells influences expression of genes involved in tissue remodelling, the observed differences were too small and too restricted in time and dose to explain the exact role of these cell types in processes leading to radiation-induced cardiac fibrosis.

摘要

目的

确定电离辐射对大鼠心脏三种不同细胞类型中转化生长因子β1(TGF-β1)、成纤维细胞生长因子2(FGF-2)、白细胞介素1β(IL-1β)、心钠素(ANP)以及I型和III型前胶原基因表达的体外效应。

材料与方法

用2.0、8.5或15 Gy的单剂量照射心肌细胞和平滑肌细胞的原代细胞培养物以及大鼠心脏内皮细胞系(RHEC)的培养物。在照射后的不同时间点(4 - 336小时),使用竞争性PCR技术分析基因表达。

结果

培养的大鼠心脏细胞照射可能导致所研究基因表达的暂时变化。对培养的心肌细胞、心脏成纤维细胞和大鼠心脏内皮细胞的辐射反应分析显示,在(1)引起mRNA表达变化所需的剂量、(2)“诱导”反应的水平和(3)持续时间方面存在不同反应。观察到的变化较小,并且在平行实验之间,诱导基因表达的起始和时间进程在4至48小时之间变化。在2.0 Gy剂量后,内皮细胞中4至48小时期间TGF-β1 mRNA的平均表达显著升高;在8.5 Gy剂量后,成纤维细胞中升高;在15 Gy剂量后,心肌细胞中升高。在8.5 Gy剂量后,观察到心肌细胞中TGF-β1 mRNA下调。在2.0 Gy剂量后,成纤维细胞中FGF-2和I型前胶原mRNA显著升高。对于所有三种细胞类型,未观察到剂量对基因表达的时间或大小有影响。

结论

尽管培养的心脏细胞照射会影响参与组织重塑的基因表达,但观察到的差异太小,且在时间和剂量上过于受限,无法解释这些细胞类型在导致放射性心脏纤维化的过程中的确切作用。

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