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用于表面活性剂生物合成的胎儿肺器官培养的优化

Optimization of fetal lung organ culture for surfactant biosynthesis.

作者信息

Doucet E, Bourbon J, Rieutort M, Marin L, Tordet C

出版信息

In Vitro Cell Dev Biol. 1987 Mar;23(3):189-98. doi: 10.1007/BF02623579.

Abstract

Lung organ culture has been a widely used system for studying differentiation and maturation of alveolar epithelium through various culture conditions. The purpose of this work was to carefully characterize in vitro lung biochemical differentiation through isolation of surfactant fraction from tissue and to search for optimal culture conditions. Fetal rat lung was explanted on the 18th gestational day for studying glycogen storage, and on the 20th gestational day for studying surfactant accretion, and cultivated for 48 h. Morphologic differentiation was studied by electron microscopy on tissue explanted on the 17th or 18th gestational days and cultivated for various times. Glycogen storage was greater on fluid medium, although less than occurring in vivo. Cellular integrity and surfactant accumulation were maximal on a semisolid medium containing 0.5% agar. Use of O2-CO2 instead of air-CO2 for gassing the explants slightly decreased phospholipid accumulation. Among media used in previous lung culture studies, Waymouth MB 752/1 was the only one to allow net glycogen accumulation in vitro. The most favorable media for surfactant phospholipid accretion were Waymouth MB 752/1, Eagle's minimum essential and its Dulbecco's modification, CMRL 1066, and NCTC 109. They allowed a 12- to 14-fold increase of surfactant fraction phospholipids in vitro, which is similar to the increase occurring in vivo during the same period. Ham's F10 and F12 media allowed a six fold increase. RPMI 1640 and medium 199 (M199) allowed only a three fold increase. Phospholipid concentration in nonsurfactant fraction only doubled during culture, and differences between various media were much less marked. DNA concentration changed little during culture. Morphologic differentiation of epithelial cells was advanced as compared with in vivo timing in a medium allowing maximal surfactant accretion (Waymouth MB 752/1) but not in a medium allowing low surfactant increase (RPMI 1640). The possible role of compositional differences between media is discussed.

摘要

肺器官培养一直是一种广泛应用的系统,用于通过各种培养条件研究肺泡上皮细胞的分化和成熟。这项工作的目的是通过从组织中分离表面活性剂组分来仔细表征体外肺生化分化,并寻找最佳培养条件。在妊娠第18天取出胎鼠肺用于研究糖原储存,在妊娠第20天取出用于研究表面活性剂积聚,并培养48小时。通过电子显微镜对在妊娠第17天或18天取出并培养不同时间的组织进行形态学分化研究。在液体培养基上糖原储存更多,尽管比体内发生的要少。在含有0.5%琼脂的半固体培养基上细胞完整性和表面活性剂积累最大。用O₂-CO₂代替空气-CO₂对组织块通气会稍微降低磷脂积累。在先前的肺培养研究中使用的培养基中,Waymouth MB 752/1是唯一能在体外允许净糖原积累的培养基。对于表面活性剂磷脂积聚最有利的培养基是Waymouth MB 752/1、伊格尔最低必需培养基及其杜尔贝科改良培养基、CMRL 1066和NCTC 109。它们能使体外表面活性剂组分磷脂增加12至14倍,这与同期体内发生的增加相似。哈姆F10和F12培养基能使表面活性剂增加6倍。RPMI 1640和199培养基(M199)仅能使表面活性剂增加3倍。非表面活性剂组分中的磷脂浓度在培养过程中仅翻倍,并且各种培养基之间的差异不太明显。培养过程中DNA浓度变化很小。与体内时间相比,在允许最大表面活性剂积聚的培养基(Waymouth MB 752/1)中上皮细胞的形态学分化有所进展,但在允许表面活性剂增加较少的培养基(RPMI 1640)中则没有。讨论了培养基成分差异可能发挥的作用。

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