胰岛素作用于成纤维细胞抑制糖皮质激素刺激肺成熟。

K S Carlson, B T Smith, M Post
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引用次数: 31

摘要

在胎儿II型细胞培养和含有II型细胞和成纤维细胞的混合细胞培养中研究了胰岛素和皮质醇对饱和磷脂酰胆碱合成的影响。在19天的胎鼠肺ⅱ型细胞培养中,100 nM的皮质醇和2 nM的胰岛素对肺ⅱ型细胞无显著影响。成纤维细胞-肺细胞因子导致胎儿II型细胞饱和磷脂酰胆碱合成增强。皮质醇在混合细胞培养中的显著刺激作用在胰岛素或成纤维细胞-肺细胞因子单克隆抗体的存在下被消除。II型细胞与暴露于皮质醇的成纤维细胞的条件培养基孵育导致饱和磷脂酰胆碱合成增加。当II型细胞与暴露于胰岛素和皮质醇(或单独暴露于胰岛素)的成纤维细胞的条件培养基孵育时,这一过程不会受到刺激。这些观察结果表明,胰岛素抑制皮质醇诱导肺成熟,并表明这种拮抗作用是由于胰岛素抑制胎儿肺成纤维细胞对成纤维细胞-肺细胞因子的细化。
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Insulin acts on the fibroblast to inhibit glucocorticoid stimulation of lung maturation.

The effects of insulin and cortisol on saturated phosphatidylcholine synthesis are examined in fetal type II cell cultures and in mixed cell cultures containing type II cells and fibroblasts. In 19-day fetal rat lung type II cell cultures, 100 nM cortisol and 2 nM insulin have no significant effect. Fibroblast-pneumonocyte factor results in enhanced saturated phosphatidylcholine synthesis by fetal type II cells. The significant stimulatory effect of cortisol in mixed-cell cultures is abolished in the presence of insulin or of monoclonal antibodies to fibroblast-pneumonocyte factor. Incubation of type II cells with conditioned media from fibroblasts exposed to cortisol results in increased saturated phosphatidylcholine synthesis. This process is not stimulated when type II cells are incubated with conditioned media from fibroblasts exposed to insulin and cortisol (or to insulin alone). These observations demonstrate that insulin inhibits cortisol induction of lung maturation and suggest that this antagonism results from an inhibitory effect of insulin on the elaboration of fibroblast-pneumonocyte factor by fetal lung fibroblasts.

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