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无血清分离细胞培养中胎鼠肺II型细胞的分化:调节与抑制

Fetal rat lung type II cell differentiation in serum-free isolated cell culture: modulation and inhibition.

作者信息

Fraslon C, Lacaze-Masmonteil T, Zupan V, Chailley-Heu B, Bourbon J R

机构信息

Centre de Biologie Cellulaire, Centre National de la Recherche Scientifique, Ivry/Seine, France.

出版信息

Am J Physiol. 1993 May;264(5 Pt 1):L504-16. doi: 10.1152/ajplung.1993.264.5.L504.

Abstract

Undifferentiated fetal rat lung epithelial cells were isolated on gestational days 15 or 17 (term 22 days) and cultured in a defined medium. On plastic, most of the cells developed structurally abnormal lamellar bodies. On a basement membrane matrix (BMM), they sequentially accumulated glycogen and formed typical lamellar bodies. Biochemical analysis of the latter indicated that they had a phospholipid composition typical of surfactant for cells on BMM but not on plastic and that surfactant protein A appeared on BMM only. Progressing maturation from day 1 to day 6 in culture was demonstrated for 17-day cells on BMM by a sevenfold increase of labeled precursor incorporation into surfactant phospholipids. Exposure to medium conditioned by 21-day fetal fibroblasts enhanced incorporation already after a 1-day culture. The antisteroid RU 486 had no effect on differentiation, whereas transforming growth factor-beta, a factor produced by lung mesenchyme at early fetal stages, inhibited it markedly. Alveolar epithelial type II cells appear to be committed early, but their maturational process would be prevented until a definite gestational stage.

摘要

未分化的胎鼠肺上皮细胞于妊娠第15天或第17天(足月为22天)分离,并在限定培养基中培养。在塑料培养皿上,大多数细胞形成结构异常的板层小体。在基底膜基质(BMM)上,它们依次积累糖原并形成典型的板层小体。对后者的生化分析表明,它们具有BMM上细胞表面活性剂典型的磷脂组成,而塑料培养皿上的细胞则没有,并且表面活性剂蛋白A仅出现在BMM上。通过将标记前体掺入表面活性剂磷脂中的量增加七倍,证明了BMM上培养的17天细胞从培养第1天到第6天的成熟过程在不断进展。暴露于21天胎鼠成纤维细胞条件培养基中,培养1天后即增强了掺入。抗类固醇RU 486对分化没有影响,而转化生长因子-β(胎儿早期肺间充质产生的一种因子)则明显抑制分化。肺泡II型上皮细胞似乎早期就已定向,但它们的成熟过程在特定的妊娠阶段之前会受到抑制。

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