心内膜
形态发生
细胞生物学
细胞质
化学
生物
生物物理学
解剖
内科学
医学
基因
生物化学
作者
Lianjie Miao,Yangyang Lu,Anika Nusrat,Guizhen Fan,Shaohua Zhang,Luqi Zhao,Chia‐Ling Wu,Hongyan Guo,T Huyen,Yi Zheng,Zhen‐Chuan Fan,Weinian Shou,Robert J. Schwartz,Yu Liu,Ashok Kumar,Haixin Sui,Irina I. Serysheva,Alan R. Burns,Leo Q. Wan,Bin Zhou
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-03-13
卷期号:387 (6739)
被引量:1
标识
DOI:10.1126/science.add3417
摘要
In the developing mammalian heart, the endocardium and the myocardium are separated by so-called cardiac jelly. Communication between the endocardium and the myocardium is essential for cardiac morphogenesis. How membrane-localized receptors and ligands achieve interaction across the cardiac jelly is not understood. Working in developing mouse cardiac morphogenesis models, we used a variety of cellular, imaging, and genetic approaches to elucidate this question. We found that myocardium and endocardium interacted directly through microstructures termed tunneling nanotube–like structures (TNTLs). TNTLs extended from cardiomyocytes (CMs) to contact endocardial cells (ECs) directly. TNTLs transported cytoplasmic proteins, transduced signals between CMs and ECs, and initiated myocardial growth toward the heart lumen to form ventricular trabeculae-like structures. Loss of TNTLs disturbed signaling interactions and, subsequently, ventricular patterning.
科研通智能强力驱动
Strongly Powered by AbleSci AI