人类肺发育异常的分子基础。

Biology of the neonate Pub Date : 2005-01-01 Epub Date: 2004-12-09 DOI:10.1159/000082595
Frederick Groenman, Sharon Unger, Martin Post
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引用次数: 84

摘要

在过去的二十年中,我们对肺发育的理解已经从解剖学基础转移到组织学基础,最近又转移到分子基础。组织间的相互作用决定了气管和肺原基的形成,规划了气道上皮的分支形态发生,并调节了上皮的分化。此外,肺的发育还受到机械和体液因素的影响。参与形态发生信号传导的调控分子包括生长因子、转录因子和细胞外基质分子。这些形态发生信号负责肺的模式和分化。我们将简要介绍早期呼吸形成、气道分支、肺血管形成和上皮分化过程中的分子信号。然后,我们将回顾人类肺部异常的异常形态发生信号,如气管食管瘘、先天性膈疝、肺增生、肺泡毛细血管发育不良、先天性囊性腺瘤样畸形和支气管肺发育不良。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The molecular basis for abnormal human lung development.

Our understanding of lung development in the past two decades has moved from an anatomical to a histological basis and, most recently, to a molecular basis. Tissue interactions specify tracheal and lung primordia formation, program branching morphogenesis of the airway epithelium and regulate epithelial differentiation. In addition, lung development is influenced by mechanical and humoral factors. The regulatory molecules involved in morphogenetic signaling include growth and transcription factors and extracellular matrix molecules. These morphogenetic signals are responsible for lung patterning and differentiation. We will provide a brief overview of molecular signaling during early respiratory formation, airway branching, pulmonary vascularization and epithelial differentiation. We will then review aberrant morphogenetic signaling in human lung abnormalities, such as tracheoesophageal fistula, congenital diaphragmatic hernia, pulmonary hyperplasia, alveolar capillary dysplasia, congenital cystic adenomatoid malformation and bronchopulmonary dysplasia.

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