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Cited2是胎儿肺成熟所必需的。

Cited2 is required for fetal lung maturation.

作者信息

Xu Bing, Qu Xiaoling, Gu Shi, Doughman Yong-Qiu, Watanabe Michiko, Dunwoodie Sally L, Yang Yu-Chung

机构信息

Department of Pharmacology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

出版信息

Dev Biol. 2008 May 1;317(1):95-105. doi: 10.1016/j.ydbio.2008.02.019. Epub 2008 Feb 26.

Abstract

Lung maturation at the terminal sac stage of lung development is characterized by a coordinated increase in terminal sac formation and vascular development in conjunction with the differentiation of alveolar type I and type II epithelial cells. The Cited2-Tcfap2a/c complex has been shown to activate transcription of Erbb3 and Pitx2c during mouse development. In this study, we show that E17.5 to E18.5 Cited2-null lungs had significantly reduced terminal sac space due to an altered differentiation of type I and type II alveolar epithelial cells. In addition, E17 Cited2-null lungs exhibited a decrease in the number of apoptotic cells, contributing to the loss in airspace. Consistent with the phenotype, genes associated with alveolar cell differentiation and survival were differentially expressed in Cited2-null fetal lungs compared to those of wild-type littermates. Moreover, expression of Cebpa, a key regulator of airway epithelial maturation, was significantly decreased in Cited2-null fetal lungs. Cited2 and Tcfap2c were present on the Cebpa promoter in E18.5 lungs to activate Cebpa transcription. We propose that the Cited2-Tcfap2c complex controls lung maturation by regulating Cebpa expression. Understanding the function of this complex may provide novel therapeutic strategies for patients with respiratory distress syndromes.

摘要

肺发育终末囊阶段的肺成熟特征在于终末囊形成和血管发育协同增加,同时伴有肺泡I型和II型上皮细胞的分化。在小鼠发育过程中,Cited2-Tcfap2a/c复合物已被证明可激活Erbb3和Pitx2c的转录。在本研究中,我们发现,由于I型和II型肺泡上皮细胞分化改变,E17.5至E18.5的Cited2基因敲除肺的终末囊空间显著减小。此外,E17的Cited2基因敲除肺中凋亡细胞数量减少,导致气腔减少。与该表型一致,与肺泡细胞分化和存活相关的基因在Cited2基因敲除的胎儿肺中与野生型同窝仔相比存在差异表达。此外,气道上皮成熟的关键调节因子Cebpa在Cited2基因敲除的胎儿肺中的表达显著降低。在E18.5肺中,Cited2和Tcfap2c存在于Cebpa启动子上以激活Cebpa转录。我们提出,Cited2-Tcfap2c复合物通过调节Cebpa表达来控制肺成熟。了解该复合物的功能可能为呼吸窘迫综合征患者提供新的治疗策略。

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