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培养的胎儿肺上皮细胞中表面活性物质蛋白和脂质合成酶的个体发生。

Ontogeny of surfactant proteins and lipid-synthesizing enzymes in cultured fetal lung epithelial cells.

作者信息

Fraslon-Vanhulle C, Chailley-Heu B, Batenburg J J, Elfring R, Bourbon J R

机构信息

Institut National de la Santé et de la Recherche Médicale U319, Unité de Développement Normal et Pathologique des Fonctions Epithéliales, Université Paris, France.

出版信息

Am J Physiol. 1994 Oct;267(4 Pt 1):L375-83. doi: 10.1152/ajplung.1994.267.4.L375.

Abstract

Fetal rat lung epithelial cells were isolated on gestational day 17 (term is 22), separated from fibroblasts, and cultured up to 6 days in a serum-free medium on a basement membrane matrix. Surfactant protein (SP) A, barely detectable by immunostaining at the beginning of the culture, considerably increased in cells and subsequently in the lumen of the epithelial cell clusters. SP-A mRNA, already detectable at culture initiation, progressively increased. By contrast, SP-B and its mRNA appeared after 2-3 days. SP-C mRNA appeared only after 4 days of culture. Cells cultured 6 days had a phospholipid composition similar to that of freshly isolated adult rat type II cells. The enhancement of lipid synthesis between the first and the sixth culture days, reported earlier to occur in these cells, was found to be accompanied by a two- to fivefold increase in amount of mRNAs of lipogenic enzymes and choline phosphate cytidylyltransferase. In conclusion, alveolar epithelial type II cells appear to be capable of full differentiation in vitro, and components of the surfactant system are all regulated developmentally at a pretranslational level.

摘要

在妊娠第17天(足月为22天)分离出胎鼠肺上皮细胞,将其与成纤维细胞分离,并在无血清培养基中的基底膜基质上培养6天。表面活性蛋白(SP)A在培养开始时通过免疫染色几乎检测不到,在细胞中显著增加,随后在上皮细胞簇的管腔中也增加。SP-A mRNA在培养开始时就已可检测到,并逐渐增加。相比之下,SP-B及其mRNA在2-3天后出现。SP-C mRNA仅在培养4天后出现。培养6天的细胞的磷脂组成与新鲜分离的成年大鼠II型细胞相似。如先前报道,在这些细胞中培养的第1天到第6天脂质合成增强,同时发现生脂酶和磷酸胆碱胞苷转移酶的mRNA量增加了2至5倍。总之,肺泡II型上皮细胞似乎能够在体外完全分化,并且表面活性剂系统的成分在翻译前水平上均受到发育调控。

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