The pericardium forms as a distinct structure during heart formation

Hannah R. Moran, Obed O. Nyarko, Rebecca O'Rourke, Ryenne-Christine R. Ching, Brisa Peña, Fréderike W. Riemslagh, Alexa Burger, Carmen C. Sucharov, Christian Mosimann
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Abstract

The heart integrates diverse cell lineages into a functional unit, including the pericardium, a mesothelial sac that supports heart movement, homeostasis, and immune responses. However, despite its critical roles, the developmental origins of the pericardium remain uncertain due to disparate models. Here, using live imaging, lineage tracking, and single-cell transcriptomics in zebrafish, we find the pericardium forms within the lateral plate mesoderm from dedicated anterior mesothelial progenitors and distinct from the classic heart field. Machine learning-based tracking and transcriptional trajectories uncover how pericardial precursors emerge among a bilateral mesothelial progenitor band to enclose the embryonic heart. This process occurs independently of heart tube formation, with canonical Wnt/β-catenin signaling modulating pericardial cell number and tissue rigidity. We link Wnt antagonist expression found in pediatric dilated cardiomyopathy to increased pericardial stiffness in a neonatal rat model. Our findings conceptually advance our models of heart formation with pericardium formation as a distinct process.
心包在心脏形成过程中形成独特的结构
心脏将不同的细胞系整合成一个功能单元,其中包括心包,它是一个支持心脏运动、稳态和免疫反应的间皮囊。然而,尽管心包起着至关重要的作用,但由于不同的模型,心包的发育起源仍不确定。在这里,我们利用斑马鱼的活体成像、品系追踪和单细胞转录组学发现,心包形成于侧板中胚层,来自专用的前间皮细胞祖细胞,有别于传统的心场。基于机器学习的追踪和转录轨迹揭示了心包前体是如何在双侧间皮细胞祖细胞带中出现并包围胚胎心脏的。这一过程与心管形成无关,典型的Wnt/β-catenin信号调节心包细胞数量和组织硬度。我们将在小儿扩张型心肌病中发现的 Wnt 拮抗剂表达与新生大鼠模型中增加的心包硬度联系起来。我们的发现从概念上推进了我们的心脏形成模型,使心包形成成为一个独特的过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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