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塑造心脏:细胞机制塑造瓣膜和小梁。

Sculpting the heart: Cellular mechanisms shaping valves and trabeculae.

机构信息

Max Planck Institute for Heart and Lung Research, Ludwigstrasse 43, Bad Nauheim 61231, Germany; German Centre for Cardiovascular Research (DZHK), Partner Site Rhine-Main, Bad Nauheim, Germany; Excellence Cluster Cardio-Pulmonary Institute (CPI), Bad Nauheim, Frankfurt, Giessen, Germany.

The Francis Crick Institute, 1 Midland Road, London NW1 1AT, UK.

出版信息

Curr Opin Cell Biol. 2021 Dec;73:26-34. doi: 10.1016/j.ceb.2021.04.009. Epub 2021 Jun 17.

DOI:10.1016/j.ceb.2021.04.009
PMID:34147705
Abstract

The transformation of the heart from a simple tube to a complex organ requires the orchestration of several morphogenetic processes. Two structures critical for cardiac function, the cardiac valves and the trabecular network, are formed through extensive tissue morphogenesis-endocardial cell migration, deadhesion and differentiation into fibroblast-like cells during valve formation, and cardiomyocyte delamination and apico-basal depolarization during trabeculation. Here, we review current knowledge of how these specialized structures acquire their shape by focusing on the underlying cellular behaviors and molecular mechanisms, highlighting findings from in vivo models and briefly discussing the recent advances in cardiac cell culture and organoids.

摘要

心脏从简单的管状结构到复杂器官的转变需要几个形态发生过程的协调。两个对心脏功能至关重要的结构,即心瓣膜和小梁网络,是通过广泛的组织形态发生形成的——在心瓣膜形成过程中,心内膜细胞迁移、去黏附和分化为成纤维样细胞,在心小梁形成过程中,心肌细胞分层和顶端-基底去极化。在这里,我们通过关注潜在的细胞行为和分子机制,回顾了这些特殊结构如何获得其形状的现有知识,重点介绍了体内模型的发现,并简要讨论了心脏细胞培养和类器官的最新进展。

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