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CCBE1 对于心肌发育过程中心外膜功能至关重要。

CCBE1 Is Essential for Epicardial Function during Myocardium Development.

机构信息

Stem Cells and Development Laboratory, iNOVA4Health, NOVA Medical School/Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, 1169-056 Lisbon, Portugal.

Medicine Department, School of Medicine, University of Cádiz (UCA), 11003 Cádiz, Spain.

出版信息

Int J Mol Sci. 2022 Oct 20;23(20):12642. doi: 10.3390/ijms232012642.

Abstract

The epicardium is a single cell layer of mesothelial cells that plays a critical role during heart development contributing to different cardiac cell types of the developing heart through epithelial-to-mesenchymal transition (EMT). Moreover, the epicardium is a source of secreted growth factors that promote myocardial growth. CCBE1 is a secreted extracellular matrix protein expressed by epicardial cells that is required for the formation of the primitive coronary plexus. However, the role of CCBE1 during epicardial development was still unknown. Here, using a knockout (KO) mouse model, we observed that loss of CCBE1 leads to congenital heart defects including thinner and hyper-trabeculated ventricular myocardium. In addition, mutant hearts displayed reduced proliferation of cardiomyocyte and epicardial cells. Epicardial outgrowth culture assay to assess epicardial-derived cells (EPDC) migration showed reduced invasion of the collagen gel by EPDCs in KO epicardial explants. KO hearts also displayed fewer nonmyocyte/nonendothelial cells intramyocardially with a reduced proliferation rate. Additionally, RNA-seq data and experimental validation by qRT-PCR showed a marked deregulation of EMT-related genes in developing mutant hearts. Together, these findings indicate that the myocardium defects in KO mice arise from disruption of epicardial development and function.

摘要

心外膜是一层单层的间皮细胞,在心发育过程中起着至关重要的作用,通过上皮-间充质转化(EMT)促进心脏发育的不同心脏细胞类型。此外,心外膜是分泌生长因子的来源,促进心肌生长。CCBE1 是心外膜细胞表达的一种分泌型细胞外基质蛋白,是原始冠状丛形成所必需的。然而,CCBE1 在心外膜发育过程中的作用尚不清楚。在这里,我们使用 基因敲除(KO)小鼠模型,观察到 CCBE1 的缺失导致先天性心脏缺陷,包括心室心肌变薄和过度小梁化。此外, 突变心脏显示心肌细胞和心外膜细胞增殖减少。心外膜外植体进行心外膜衍生细胞(EPDC)迁移评估的外植体培养试验显示,EPDC 在 KO 心外膜外植体中的胶原凝胶侵袭减少。 KO 心脏还显示心肌内非心肌细胞/非内皮细胞数量减少,增殖速度减慢。此外,RNA-seq 数据和 qRT-PCR 的实验验证表明,发育中的 突变心脏 EMT 相关基因的表达明显失调。综上所述,这些发现表明 KO 小鼠的心肌缺陷是由于心外膜发育和功能的破坏引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e2b/9604378/a570920ee091/ijms-23-12642-g001.jpg

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