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纤连蛋白在人肾小球系膜细胞培养物中的表达及其受阿霉素的影响。

Fibronectin expression in human mesangial cell cultures and its alterations by adriamycin.

作者信息

Soose M, Wenzel S, Padur A, Oberst D, Stolte H

机构信息

Institute of Animal Physiology, Justus-Liebig University Giessen, Germany.

出版信息

Cell Biol Toxicol. 1995 Feb;11(1):51-63. doi: 10.1007/BF00769992.

DOI:10.1007/BF00769992
PMID:7600259
Abstract

Human mesangial cell (HMC) cultures synthesize cellular fibronectin (FN), which is secreted and incorporated into a fibrillar extracellular matrix (ECM). The anticancer drug adriamycin (ADR) induces changes in extracellular FN deposition. As revealed by immunofluorescence staining, a 24 h incubation of the cells with 2 micrograms ADR/ml resulted in a marked expansion of the pericellular FN fibers, which may be due to either an increased synthesis or a decreased FN degradation. The effects of ADR on FN mRNA were analysed by northern hybridization and in vitro translation. Steady-state FN mRNA levels were significantly increased by 60% following ADR administration. However, yields of radioactivity incorporated into FN by cell-free translation remained constant (2.3 +/- 0.7%, n = 24, vs controls 2.2 +/- 0.8% of total radioactivity, n = 23). The quality of translation products was not affected by the drug, whereas translation efficiency of total RNA from ADR-treated HMC was only 75% of controls. The data presented suggest a negative feedback control of FN expression on the level of translation. Extracellular FN accumulation in the experimental model of ADR-induced progressive glomerulopathy therefore cannot be explained by an increased FN synthesis, but is rather regarded a consequence of proteinase inhibition. This assumption is compatible with a diminished number of FN fragments recently demonstrated in the culture medium of ADR-treated HMC, and is further corroborated by the loss of urinary FN degradation products accompanying the onset of proteinuria in ADR-treated rats.

摘要

人系膜细胞(HMC)培养物可合成细胞纤连蛋白(FN),该蛋白分泌后整合到纤维状细胞外基质(ECM)中。抗癌药物阿霉素(ADR)可诱导细胞外FN沉积发生变化。免疫荧光染色显示,细胞在含2微克ADR/毫升的培养液中孵育24小时后,细胞周围的FN纤维显著扩展,这可能是由于合成增加或FN降解减少所致。通过Northern杂交和体外翻译分析了ADR对FN mRNA的影响。给予ADR后,稳态FN mRNA水平显著增加了60%。然而,无细胞翻译掺入FN的放射性产量保持恒定(2.3±0.7%,n = 24,与对照组相比,占总放射性的2.2±0.8%,n = 23)。翻译产物的质量不受药物影响,而ADR处理的HMC总RNA的翻译效率仅为对照组的75%。所呈现的数据表明在翻译水平上存在对FN表达的负反馈控制。因此,在ADR诱导的进行性肾小球病实验模型中,细胞外FN积累不能用FN合成增加来解释,而应被视为蛋白酶抑制的结果。这一假设与最近在ADR处理的HMC培养基中显示的FN片段数量减少相一致,并且在ADR处理的大鼠中蛋白尿发作时伴随尿FN降解产物的丧失进一步得到了证实。

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