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出生时肺成熟需要C/EBPα。

C/EBPalpha is required for lung maturation at birth.

作者信息

Martis Prithy C, Whitsett Jeffrey A, Xu Yan, Perl Anne-Karina T, Wan Huajing, Ikegami Machiko

机构信息

Division of Pulmonary Biology and Neonatology, Cincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.

出版信息

Development. 2006 Mar;133(6):1155-64. doi: 10.1242/dev.02273. Epub 2006 Feb 8.

Abstract

Epithelial cells lining the peripheral lung synthesize pulmonary surfactant that reduces surface tension at the air-liquid interface. Lack of surfactant lipids and proteins in the lungs causes respiratory distress syndrome, a common cause of morbidity and mortality in preterm infants. We show that C/EBPalpha plays a crucial role in the maturation of the respiratory epithelium in late gestation, being required for the production of surfactant lipids and proteins necessary for lung function. Deletion of the Cebpa gene in respiratory epithelial cells in fetal mice caused respiratory failure at birth. Structural and biochemical maturation of the lung was delayed. Normal synthesis of surfactant lipids and proteins, including SP-A, SP-B, SP-C, SP-D, ABCA3 (a lamellar body associated protein) and FAS (precursor of fatty acid synthesis) were dependent upon expression of the C/EBPalpha in respiratory epithelial cells. Deletion of the Cebpa gene caused increased expression of Tgfb2, a growth factor that inhibits lung epithelial cell proliferation and differentiation. Normal expression of C/EBPalpha required Titf1 and Foxa2, transcription factors that also play an important role in perinatal lung differentiation. C/EBPalpha participates in a transcriptional network that is required for the regulation of genes mediating perinatal lung maturation and surfactant homeostasis that is necessary for adaptation to air breathing at birth.

摘要

肺外周的上皮细胞合成肺表面活性物质,可降低气液界面的表面张力。肺部缺乏表面活性物质脂质和蛋白质会导致呼吸窘迫综合征,这是早产儿发病和死亡的常见原因。我们发现,C/EBPα在妊娠后期呼吸上皮的成熟过程中起关键作用,是肺功能所需的表面活性物质脂质和蛋白质产生所必需的。在胎鼠的呼吸上皮细胞中删除Cebpa基因会导致出生时呼吸衰竭。肺的结构和生化成熟延迟。表面活性物质脂质和蛋白质的正常合成,包括SP-A、SP-B、SP-C、SP-D、ABCA3(一种板层小体相关蛋白)和FAS(脂肪酸合成前体)依赖于呼吸上皮细胞中C/EBPα的表达。删除Cebpa基因会导致Tgfb2表达增加,Tgfb2是一种抑制肺上皮细胞增殖和分化的生长因子。C/EBPα的正常表达需要Titf1和Foxa2,这两种转录因子在围产期肺分化中也起重要作用。C/EBPα参与一个转录网络,该网络对于调节介导围产期肺成熟和表面活性物质稳态的基因是必需的,而表面活性物质稳态是出生时适应空气呼吸所必需的。

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