Macrophage lineages in heart development and regeneration.

2区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Current Topics in Developmental Biology Pub Date : 2024-01-01 Epub Date: 2024-02-24 DOI:10.1016/bs.ctdb.2024.01.004
Na Xu, Brittany A Gonzalez, Katherine E Yutzey
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引用次数: 0

Abstract

During development, macrophage subpopulations derived from hematopoietic progenitors take up residence in the developing heart. Embryonic macrophages are detectable at the early stages of heart formation in the nascent myocardium, valves and coronary vasculature. The specific subtypes of macrophages present in the developing heart reflect the generation of hematopoietic progenitors in the yolk sac, aorta-gonad-mesonephros, fetal liver, and postnatal bone marrow. Ablation studies have demonstrated specific requirements for embryonic macrophages in valve remodeling, coronary and lymphatic vessel development, specialized conduction system maturation, and myocardial regeneration after neonatal injury. The developmental origins of macrophage lineages change over time, with embryonic lineages having more reparative and remodeling functions in comparison to the bone marrow derived myeloid lineages of adults. Here we review the contributions and functions of cardiac macrophages in the developing heart with potential regenerative and reparative implications for cardiovascular disease.

心脏发育和再生过程中的巨噬细胞系
在发育过程中,来自造血祖细胞的巨噬细胞亚群会在发育中的心脏中定居。在心脏形成的早期阶段,新生心肌、瓣膜和冠状血管中就能检测到胚胎巨噬细胞。发育中心脏中巨噬细胞的特定亚型反映了造血祖细胞在卵黄囊、主动脉-性腺-肾上腺、胎儿肝脏和出生后骨髓中的生成情况。消融研究表明,在瓣膜重塑、冠状动脉和淋巴管发育、特殊传导系统成熟和新生儿损伤后心肌再生中,对胚胎巨噬细胞有特殊要求。巨噬细胞系的发育起源会随着时间的推移而改变,与成人骨髓衍生的髓系相比,胚胎系具有更多的修复和重塑功能。在此,我们回顾了心脏巨噬细胞在心脏发育过程中的贡献和功能,以及对心血管疾病的潜在再生和修复意义。
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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来源期刊
CiteScore
6.00
自引率
0.00%
发文量
91
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