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心脏神经嵴细胞:它们的神经节段特异性、迁移以及与心脏和大血管异常的关联。

Cardiac Neural Crest Cells: Their Rhombomeric Specification, Migration, and Association with Heart and Great Vessel Anomalies.

机构信息

Department of Cardiovascular Surgery Adult and Pediatric, Geneva University Hospital, Geneva, Switzerland.

Cardiovascular Research Laboratory, Faculty of Medicine of the University of Geneva, Rue Michel Servet 1, 1211, Geneva 4, Switzerland.

出版信息

Cell Mol Neurobiol. 2021 Apr;41(3):403-429. doi: 10.1007/s10571-020-00863-w. Epub 2020 May 13.

Abstract

Outflow tract abnormalities are the most frequent congenital heart defects. These are due to the absence or dysfunction of the two main cell types, i.e., neural crest cells and secondary heart field cells that migrate in opposite directions at the same stage of development. These cells directly govern aortic arch patterning and development, ascending aorta dilatation, semi-valvular and coronary artery development, aortopulmonary septation abnormalities, persistence of the ductus arteriosus, trunk and proximal pulmonary arteries, sub-valvular conal ventricular septal/rotational defects, and non-compaction of the left ventricle. In some cases, depending on the functional defects of these cells, additional malformations are found in the expected spatial migratory area of the cells, namely in the pharyngeal arch derivatives and cervico-facial structures. Associated non-cardiovascular anomalies are often underestimated, since the multipotency and functional alteration of these cells can result in the modification of multiple neural, epidermal, and cervical structures at different levels. In most cases, patients do not display the full phenotype of abnormalities, but congenital cardiac defects involving the ventricular outflow tract, ascending aorta, aortic arch and supra-aortic trunks should be considered as markers for possible impaired function of these cells. Neural crest cells should not be considered as a unique cell population but on the basis of their cervical rhombomere origins R3-R5 or R6-R7-R8 and specific migration patterns: R3-R4 towards arch II, R5-R6 arch III and R7-R8 arch IV and VI. A better understanding of their development may lead to the discovery of unknown associated abnormalities, thereby enabling potential improvements to be made to the therapeutic approach.

摘要

流出道异常是最常见的先天性心脏缺陷。这些缺陷是由于两种主要细胞类型的缺失或功能障碍引起的,即神经嵴细胞和次级心脏场细胞,它们在发育的同一阶段向相反方向迁移。这些细胞直接控制主动脉弓模式和发育、升主动脉扩张、半月瓣和冠状动脉发育、主肺动脉隔异常、动脉导管持续存在、干和近端肺动脉、瓣下圆锥室间隔/旋转缺陷以及左心室非致密化。在某些情况下,取决于这些细胞的功能缺陷,在细胞预期的空间迁移区域中还会发现其他畸形,即在咽弓衍生物和颈面部结构中。相关的非心血管异常通常被低估,因为这些细胞的多能性和功能改变可能导致多个神经、表皮和颈部结构在不同水平上发生改变。在大多数情况下,患者不会表现出异常的全部表型,但涉及心室流出道、升主动脉、主动脉弓和主动脉弓以上干的先天性心脏缺陷应被视为这些细胞功能受损的可能标志物。神经嵴细胞不应被视为单一的细胞群体,而应根据其颈部菱脑节的起源 R3-R5 或 R6-R7-R8 以及特定的迁移模式:R3-R4 向弓 II 迁移,R5-R6 向弓 III 迁移,R7-R8 向弓 IV 和 VI 迁移。对它们发育的更好理解可能会导致发现未知的相关异常,从而能够对治疗方法进行潜在的改进。

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