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博来霉素诱导的大鼠肺纤维化发育过程中小蛋白聚糖、胶原蛋白和转化生长因子-β1的表达改变

Altered expression of small proteoglycans, collagen, and transforming growth factor-beta 1 in developing bleomycin-induced pulmonary fibrosis in rats.

作者信息

Westergren-Thorsson G, Hernnäs J, Särnstrand B, Oldberg A, Heinegård D, Malmström A

机构信息

Department of Physiological Chemistry, Lund University, Sweden.

出版信息

J Clin Invest. 1993 Aug;92(2):632-7. doi: 10.1172/JCI116631.

Abstract

The development of bleomycin-induced pulmonary fibrosis in rats was studied over a period of 21 d after an intratracheal instillation of bleomycin. The expression of three small proteoglycans (biglycan, decorin, and fibromodulin), collagen III and TGF-beta 1 was studied by RNA-transfer blot analysis. The proteoglycans were also studied by SDS-polyacrylamide gel electrophoresis and Western blots. TGF-beta 1 mRNA increased threefold already on day 3 and remained elevated until day 10. After the increase of TGF-beta 1 mRNA the messages for biglycan and collagen III steadily increased to reach a maximum 10 d after bleomycin instillation. The mRNA for biglycan increased maximally fourfold and that of collagen III 2.5-fold. Decorin mRNA, in contrast to biglycan decreased and reached 20% of control on day 10. The message for fibromodulin remained constant throughout the study period. The amounts of biglycan and decorin in the tissue changed in accordance with the mRNA levels. The results corroborate and extend previous in vitro studies concerning the effect of TGF-beta 1 on the metabolism of small proteoglycans and show that these macromolecules are regulated differently also in vivo. The marked alterations of biglycan and decorin during the development of fibrosis suggests that these proteoglycans have a regulating role in this process.

摘要

在气管内注入博来霉素后21天的时间里,研究了大鼠博来霉素诱导性肺纤维化的发展情况。通过RNA转移印迹分析研究了三种小蛋白聚糖(双糖链蛋白聚糖、核心蛋白聚糖和纤调蛋白聚糖)、Ⅲ型胶原蛋白和转化生长因子β1(TGF-β1)的表达。还通过SDS-聚丙烯酰胺凝胶电泳和蛋白质免疫印迹法对蛋白聚糖进行了研究。TGF-β1 mRNA在第3天就增加了三倍,并一直升高到第10天。在TGF-β1 mRNA增加后,双糖链蛋白聚糖和Ⅲ型胶原蛋白的信息稳步增加,在博来霉素注入后10天达到最大值。双糖链蛋白聚糖的mRNA最大增加了四倍,Ⅲ型胶原蛋白的mRNA增加了2.5倍。相比之下,核心蛋白聚糖的mRNA减少,在第10天降至对照的20%。在整个研究期间,纤调蛋白聚糖的信息保持不变。组织中双糖链蛋白聚糖和核心蛋白聚糖的量根据mRNA水平而变化。这些结果证实并扩展了先前关于TGF-β1对小蛋白聚糖代谢影响的体外研究,并表明这些大分子在体内也受到不同的调节。在纤维化发展过程中双糖链蛋白聚糖和核心蛋白聚糖的显著变化表明这些蛋白聚糖在这个过程中具有调节作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/493e/294895/fa9920c3e5f1/jcinvest00029-0108-a.jpg

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