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肺周细胞调节肺形态发生。

Pulmonary pericytes regulate lung morphogenesis.

机构信息

Department of Tissue Morphogenesis, Max Planck Institute for Molecular Biomedicine, and University of Münster, Faculty of Medicine, D-48149, Münster, Germany.

Center for Vascular Research, Institute of Basic Science (IBS), Daejeon, 34141, Republic of Korea.

出版信息

Nat Commun. 2018 Jun 22;9(1):2448. doi: 10.1038/s41467-018-04913-2.

Abstract

Blood vessels are essential for blood circulation but also control organ growth, homeostasis, and regeneration, which has been attributed to the release of paracrine signals by endothelial cells. Endothelial tubules are associated with specialised mesenchymal cells, termed pericytes, which help to maintain vessel wall integrity. Here we identify pericytes as regulators of epithelial and endothelial morphogenesis in postnatal lung. Mice lacking expression of the Hippo pathway components YAP and TAZ in pericytes show defective alveologenesis. Mutant pericytes are present in normal numbers but display strongly reduced expression of hepatocyte growth factor leading to impaired activation of the c-Met receptor, which is expressed by alveolar epithelial cells. YAP and TAZ are also required for expression of angiopoietin-1 by pulmonary pericytes, which also controls hepatocyte growth factor expression and thereby alveologenesis in an autocrine fashion. These findings establish that pericytes have important, organ-specific signalling properties and coordinate the behavior of epithelial and vascular cells during lung morphogenesis.

摘要

血管对于血液循环至关重要,但也控制着器官的生长、稳态和再生,这归因于内皮细胞释放的旁分泌信号。内皮小管与称为周细胞的专门间充质细胞相关联,周细胞有助于维持血管壁的完整性。在这里,我们确定周细胞是出生后肺中上皮细胞和内皮细胞形态发生的调节剂。周细胞中 Hippo 通路成分 YAP 和 TAZ 缺失表达的小鼠表现出肺泡生成缺陷。突变周细胞的数量正常,但表达的肝细胞生长因子明显减少,导致其表达的 c-Met 受体激活受损,c-Met 受体由肺泡上皮细胞表达。YAP 和 TAZ 对于肺周细胞中血管生成素 1 的表达也是必需的,血管生成素 1 也以自分泌的方式控制肝细胞生长因子的表达和肺泡生成。这些发现确立了周细胞具有重要的、器官特异性的信号特性,并在肺形态发生过程中协调上皮细胞和血管细胞的行为。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9782/6015030/090aeba1d956/41467_2018_4913_Fig1_HTML.jpg

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