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心肌梗死后,内皮细胞的可塑性驱动心内膜中的动脉重塑。

Endothelial plasticity drives arterial remodeling within the endocardium after myocardial infarction.

机构信息

From Aix Marseille Université, CNRS, IBDM UMR 7288, Marseille, France (L.M., R.S., R.G.K.); and PHYMEDEXP, Physiologie et Médecine Expérimentale Cœur et Muscles, INSERM U1046, CNRS UMR 9214, Université de Montpellier, CHU Arnaud de Villeneuve, Montpellier, France (J.T., P.B, S.R.).

出版信息

Circ Res. 2015 May 22;116(11):1765-71. doi: 10.1161/CIRCRESAHA.116.306476. Epub 2015 Apr 1.

Abstract

RATIONALE

Revascularization of injured, ischemic, and regenerating organs is essential to restore organ function. In the postinfarct heart, however, the mechanisms underlying the formation of new coronary arteries are poorly understood.

OBJECTIVE

To study vascular remodeling of coronary arteries after infarction.

METHODS AND RESULTS

We performed permanent left coronary ligation on Connexin40-GFP mice expressing green fluorescent protein (GFP) in endothelial cells of coronary arteries but not veins, capillaries, or endocardium. GFP(+) endothelial foci were identified within the endocardium in the infarct zone. These previously undescribed structures, termed endocardial flowers, have a distinct endothelial phenotype (Cx40(+), VEGFR2(+), and endoglin(-)) to the surrounding endocardium (Cx40(-), VEGFR2(-), and endoglin(+)). Endocardial flowers are contiguous with coronary vessels and associated with subendocardial smooth muscle cell accumulation. Genetic lineage tracing reveals extensive endothelial plasticity in the postinfarct heart, showing that endocardial flowers develop by arteriogenesis of Cx40(-) cells and by outgrowth of pre-existing coronary arteries. Finally, endocardial flowers exhibit angiogenic features, including early VEGFR2 expression and active proliferation of adjacent endocardial and smooth muscle cells.

CONCLUSIONS

Arterial endothelial foci within the endocardium reveal extensive endothelial cell plasticity in the infarct zone and identify the endocardium as a site of endogenous arteriogenesis and source of endothelial cells to promote vascularization in regenerative strategies.

摘要

理由

受伤、缺血和再生器官的再血管化对于恢复器官功能至关重要。然而,在心肌梗死后,新冠状动脉形成的机制仍知之甚少。

目的

研究梗死后冠状动脉的血管重塑。

方法和结果

我们对 Connexin40-GFP 小鼠进行了永久性左冠状动脉结扎,该小鼠的 GFP 在冠状动脉内皮细胞中表达,但不在静脉、毛细血管或心内膜中表达。GFP(+)内皮灶在心梗区的心内膜中被鉴定出来。这些以前未被描述的结构,称为心内膜花,与周围的心内膜具有明显的内皮表型(Cx40(+)、VEGFR2(+)和内格林(-))(Cx40(-)、VEGFR2(-)和内格林(+))。心内膜花与冠状动脉相连,并与心内膜下平滑肌细胞积聚有关。遗传谱系追踪显示,梗死后心脏内皮细胞具有广泛的可塑性,表明心内膜花是通过 Cx40(-)细胞的动脉生成和预先存在的冠状动脉的生长而形成的。最后,心内膜花表现出血管生成特征,包括早期 VEGFR2 表达和相邻心内膜和平滑肌细胞的活跃增殖。

结论

心内膜内的动脉内皮灶揭示了梗塞区内皮细胞的广泛可塑性,并确定了心内膜作为内源性动脉生成的部位和内皮细胞的来源,以促进再生策略中的血管化。

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