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Eve阳性心包细胞的不同亚群可稳定心脏流出道,并在……中促进Hox基因触发的心脏形态发生。

Distinct subsets of Eve-positive pericardial cells stabilise cardiac outflow and contribute to Hox gene-triggered heart morphogenesis in .

作者信息

Zmojdzian Monika, de Joussineau Svetlana, Da Ponte Jean Philippe, Jagla Krzysztof

机构信息

GReD - INSERM U1103, CNRS UMR6293, University of Clermont Auvergne, 63000 Clermont-Ferrand, France

GReD - INSERM U1103, CNRS UMR6293, University of Clermont Auvergne, 63000 Clermont-Ferrand, France.

出版信息

Development. 2018 Jan 17;145(2):dev158717. doi: 10.1242/dev.158717.

DOI:10.1242/dev.158717
PMID:29247145
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5825839/
Abstract

The heart, composed of discrete subsets of cardioblasts and pericardial cells, undergoes Hox-triggered anterior-posterior morphogenesis, leading to a functional subdivision into heart proper and aorta, with its most anterior part forming a funnel-shaped cardiac outflow. Cardioblasts differentiate into Tin-positive 'working myocytes' and Svp-expressing ostial cells. However, developmental fates and functions of heart-associated pericardial cells remain elusive. Here, we show that the pericardial cells that express the transcription factor Even Skipped adopt distinct fates along the anterior-posterior axis. Among them, the most anterior Antp-Ubx-AbdAnegative cells form a novel cardiac outflow component we call the outflow hanging structure, whereas the Antp-expressing cells differentiate into wing heart precursors. Interestingly, gene expression in the Even Skipped-positive cells not only underlies their antero-posterior diversification, but also influences heart morphogenesis in a non-cell-autonomous way. In brief, we identify a new cardiac outflow component derived from a subset of Even Skipped-expressing cells that stabilises the anterior heart tip, and demonstrate non-cell-autonomous effects of Hox gene expression in the Even Skipped-positive cells on heart morphogenesis.

摘要

心脏由成心肌细胞和心包细胞的离散亚群组成,经历由Hox触发的前后形态发生,导致功能性地细分为心脏本体和主动脉,其最前部形成漏斗状的心脏流出道。成心肌细胞分化为Tin阳性的“工作心肌细胞”和表达Svp的开口细胞。然而,与心脏相关的心包细胞的发育命运和功能仍然不清楚。在这里,我们表明表达转录因子Even Skipped的心包细胞沿前后轴采用不同的命运。其中,最前部的Antp-Ubx-AbdA阴性细胞形成一种新的心脏流出道成分,我们称之为流出悬挂结构,而表达Antp的细胞分化为翼状心脏前体。有趣的是,Even Skipped阳性细胞中的基因表达不仅是其前后分化的基础,还以非细胞自主的方式影响心脏形态发生。简而言之,我们鉴定出一种源自表达Even Skipped的细胞亚群的新的心脏流出道成分,它稳定了心脏尖端前部,并证明了Even Skipped阳性细胞中Hox基因表达对心脏形态发生的非细胞自主作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/77b2019198cd/develop-145-158717-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/929c79dc1a4b/develop-145-158717-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/5df9c135b75e/develop-145-158717-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/441c5d1c35de/develop-145-158717-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/77b2019198cd/develop-145-158717-g4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/929c79dc1a4b/develop-145-158717-g1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/5df9c135b75e/develop-145-158717-g2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/441c5d1c35de/develop-145-158717-g3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d94/5825839/77b2019198cd/develop-145-158717-g4.jpg

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本文引用的文献

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Embryonic heart progenitors and cardiogenesis.胚胎心脏祖细胞与心脏发生。
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Epicardial progenitor cells in cardiac development and regeneration.心外膜祖细胞在心脏发育和再生中的作用。
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