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[肺泡II型细胞增殖与表面活性物质基因表达的调控]

[Regulation of alveolar type II cell proliferation and surfactant gene expression].

作者信息

Sugahara K

机构信息

Department of Anesthesiology, Kumamoto University School of Medicine, Japan.

出版信息

Nihon Kyobu Shikkan Gakkai Zasshi. 1994 Dec;32 Suppl:73-8.

PMID:7602847
Abstract

Alveolar reorganization after lung injury essentially depends on regeneration of alveolar epithelial cells during the tissue repair. Proliferation and differentiation of alveolar type II cells are therefore fundamental mechanisms in the repair and restoration of normal lung function after lung injury. We examined the combined effects of the extracellular matrix and soluble factors on proliferation and differentiation of alveolar type II cells in vitro, and found them to be more pronounced than those of either element by itself. We also found that rat alveolar type II cells proliferating in vitro can concurrently express different surfactant protein mRNAs. In an in vivo study, we examined the expression of surfactant protein genes in streptozotocin-induced diabetic lungs and in proliferating alveolar type II cells of rats with endotoxin--induced lung injury. The results show that SP-A, SP-B, and SP-C mRNAs are expressed at different levels in both alveoan and bronchiolar epithelial cells from diabetic lungs. They also show that endotoxin can induce marked proliferation of alveolar type II cells, in association with the increased SP-A production and overexpression of SP-A, SP-B, and SP-C mRNAs soon after lung injury. These results suggest that proliferation of alveolar type II cells may play a protective role, by repairing damaged alveoli and rapidly replenishing surfactant proteins.

摘要

肺损伤后的肺泡重塑本质上取决于组织修复过程中肺泡上皮细胞的再生。因此,II型肺泡细胞的增殖和分化是肺损伤后修复和恢复正常肺功能的基本机制。我们在体外研究了细胞外基质和可溶性因子对II型肺泡细胞增殖和分化的联合作用,发现它们的作用比单独任何一种因素都更显著。我们还发现,体外增殖的大鼠II型肺泡细胞可同时表达不同的表面活性物质蛋白mRNA。在一项体内研究中,我们检测了链脲佐菌素诱导的糖尿病肺以及内毒素诱导的肺损伤大鼠增殖的II型肺泡细胞中表面活性物质蛋白基因的表达。结果显示,糖尿病肺的肺泡和细支气管上皮细胞中SP-A、SP-B和SP-C mRNA的表达水平各不相同。结果还显示,内毒素可诱导II型肺泡细胞显著增殖,且在肺损伤后不久,伴随着SP-A产量的增加以及SP-A、SP-B和SP-C mRNA的过表达。这些结果表明,II型肺泡细胞的增殖可能通过修复受损肺泡和快速补充表面活性物质蛋白发挥保护作用。

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