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

Author:

Fraslon C.1,Lacaze-Masmonteil T.1,Zupan V.1,Chailley-Heu B.1,Bourbon J. R.1

Affiliation:

1. Centre de Biologie Cellulaire, Centre National de la RechercheScientifique, Ivry/Seine, France.

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.

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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3. Rescue of the Hypoplastic Lung by Prenatal Cyclical Strain;American Journal of Respiratory and Critical Care Medicine;2005-06-15

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