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博来霉素诱导大鼠肺透明质酸生成增加的相关机制研究

Characterization of the mechanism involved in bleomycin-induced increased hyaluronan production in rat lung.

作者信息

Teder P, Nettelbladt O, Heldin P

机构信息

Department of Medical and Physiological Chemistry, Uppsala University, Sweden.

出版信息

Am J Respir Cell Mol Biol. 1995 Feb;12(2):181-9. doi: 10.1165/ajrcmb.12.2.7532420.

Abstract

The molecular mechanisms behind the accumulation of hyaluronan during bleomycin-induced lung injury in rats were investigated. The stimulatory effects of bronchoalveolar lavage fluid (BALF) and alveolar macrophage (AM)-conditioned media on hyaluronan synthesis in normal rat lung fibroblast cultures were studied as well as the hyaluronan binding activity on AM. BALF obtained on days 1 and 5 after bleomycin instillation exhibited hyaluronan stimulatory activity similar to that of 10% fetal serum; the activity returned to control values on day 14 after bleomycin treatment. Conditioned media from cultures of AM obtained from bleomycin-treated rats exhibited stimulatory effects higher than that of media from AM of control rats and equal to or higher than that of 10% fetal calf serum. The stimulatory activity in BALF was significantly inhibited by neutralizing antibodies against transforming growth factor-beta; the activity in AM-conditioned media was only partially affected. Neutralizing antibodies against platelet-derived growth factor-BB or -AA had no such inhibiting effect. Interestingly, AM from bleomycin-treated rats exhibited low hyaluronan binding activity. [3H]Hyaluronan binding by AM on days 1 and 5 after bleomycin administration was about 2-fold and 4-fold lower, respectively, compared with that by AM derived from saline-treated rats. This decrease was normalized 14 days after bleomycin treatment. In conclusion, our results indicate that factors with high potential to stimulate hyaluronan synthesis in rat lung fibroblasts are accumulated in BALF from bleomycin-treated rats and that AM are likely to be one source of such stimulatory factors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了博来霉素诱导的大鼠肺损伤过程中透明质酸积累背后的分子机制。研究了支气管肺泡灌洗液(BALF)和肺泡巨噬细胞(AM)条件培养基对正常大鼠肺成纤维细胞培养物中透明质酸合成的刺激作用以及AM上的透明质酸结合活性。博来霉素滴注后第1天和第5天获得的BALF表现出与10%胎牛血清相似的透明质酸刺激活性;博来霉素治疗后第14天该活性恢复到对照值。来自博来霉素处理大鼠的AM培养物的条件培养基表现出高于对照大鼠AM培养基的刺激作用,且等于或高于10%胎牛血清的刺激作用。BALF中的刺激活性被针对转化生长因子-β的中和抗体显著抑制;AM条件培养基中的活性仅受到部分影响。针对血小板衍生生长因子-BB或-AA的中和抗体没有这种抑制作用。有趣的是,博来霉素处理大鼠的AM表现出低透明质酸结合活性。与盐水处理大鼠的AM相比,博来霉素给药后第1天和第5天AM对[3H]透明质酸的结合分别降低了约2倍和4倍。博来霉素治疗14天后这种降低恢复正常。总之,我们的结果表明,在博来霉素处理大鼠的BALF中积累了对大鼠肺成纤维细胞中透明质酸合成具有高刺激潜力的因子,并且AM可能是此类刺激因子的一个来源。(摘要截短至250字)

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