干细胞生态位相关生物标志物在人三尖瓣基部的表达。

IF 2.5 3区 医学 Q3 CELL & TISSUE ENGINEERING
Jacob Sjölin, Marianne Jonsson, Charlotta Orback, Anders Oldfors, Anders Jeppsson, Jane Synnergren, Victoria Rotter Sopasakis, Kristina Vukusic
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引用次数: 0

摘要

干细胞壁龛已经在具有高再生能力的组织中进行了彻底的研究,但在细胞更新缓慢的组织(如人类心脏)中却没有。左房室交界处(AVj)是二尖瓣的底部,以前曾被认为是成人心脏祖细胞的利基区域。在本研究中,我们探索了人类心脏的右侧,即三尖瓣的基部,以研究该区域作为祖细胞生态位的潜力。从多器官供者(N = 12)收集了移植的人类心脏的配对活检。利用RNA测序技术比较AVj外侧、右心房(RA)和右心室(RV)干细胞壁龛相关生物标志物的表达。基因表达数据显示,与胚胎发育和细胞外基质(ECM)组成相关的基因在拟议的生态位区域,即AVj上调。此外,免疫组化显示同一区域内胎儿心脏标志物MDR1、SSEA4和WT1高表达。检测到HIF1α的核表达提示缺氧。增殖标记物PCNA和Ki67与心肌细胞核标记物PCM1和心肌肌钙蛋白T (cTnT)共染色发现罕见细胞,提示小心肌细胞增殖。WT1+/cTnT+和SSEA4+/cTnT+细胞也被发现,提示心肌细胞特异性祖细胞。随着离三尖瓣的距离,干细胞标记物的表达逐渐降低。在RV组织中未观察到这些标志物的表达。总之,三尖瓣的基部是一个富含ecm的区域,含有表达几种干细胞利基相关标记的细胞。干细胞标记物与cTnT的共表达表明心肌细胞特异性祖细胞。我们之前报道了二尖瓣底部的类似数据,因此提出成人心肌细胞祖细胞存在于两个房室瓣周围。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Expression of Stem Cell Niche-Related Biomarkers at the Base of the Human Tricuspid Valve.

Expression of Stem Cell Niche-Related Biomarkers at the Base of the Human Tricuspid Valve.

Expression of Stem Cell Niche-Related Biomarkers at the Base of the Human Tricuspid Valve.

Expression of Stem Cell Niche-Related Biomarkers at the Base of the Human Tricuspid Valve.

Stem cell niches have been thoroughly investigated in tissue with high regenerative capacity but not in tissues where cell turnover is slow, such as the human heart. The left AtrioVentricular junction (AVj), the base of the mitral valve, has previously been proposed as a niche region for cardiac progenitors in the adult human heart. In the present study, we explore the right side of the human heart, the base of the tricuspid valve, to investigate the potential of this region as a progenitor niche. Paired biopsies from explanted human hearts were collected from multi-organ donors (N = 12). The lateral side of the AVj, right atria (RA), and right ventricle (RV) were compared for the expression of stem cell niche-related biomarkers using RNA sequencing. Gene expression data indicated upregulation of genes related to embryonic development and extracellular matrix (ECM) composition in the proposed niche region, that is, the AVj. In addition, immunohistochemistry showed high expression of the fetal cardiac markers MDR1, SSEA4, and WT1 within the same region. Nuclear expression of HIF1α was detected suggesting hypoxia. Rare cells were found with the co-staining of the proliferation marker PCNA and Ki67 with cardiomyocyte nuclei marker PCM1 and cardiac Troponin T (cTnT), indicating proliferation of small cardiomyocytes. WT1+/cTnT+ and SSEA4+/cTnT+ cells were also found, suggesting cardiomyocyte-specific progenitors. The expression of the stem cell markers gradually decreased with distance from the tricuspid valve. No expression of these markers was observed in the RV tissue. In summary, the base of the tricuspid valve is an ECM-rich region containing cells with expression of several stem cell niche-associated markers. Co-expression of stem cell markers with cTnT indicates cardiomyocyte-specific progenitors. We previously reported similar data from the base of the mitral valve and thus propose that human adult cardiomyocyte progenitors reside around both atrioventricular valves.

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来源期刊
Stem cells and development
Stem cells and development 医学-细胞与组织工程
CiteScore
7.80
自引率
2.50%
发文量
69
审稿时长
3 months
期刊介绍: Stem Cells and Development is globally recognized as the trusted source for critical, even controversial coverage of emerging hypotheses and novel findings. With a focus on stem cells of all tissue types and their potential therapeutic applications, the Journal provides clinical, basic, and translational scientists with cutting-edge research and findings. Stem Cells and Development coverage includes: Embryogenesis and adult counterparts of this process Physical processes linking stem cells, primary cell function, and structural development Hypotheses exploring the relationship between genotype and phenotype Development of vasculature, CNS, and other germ layer development and defects Pluripotentiality of embryonic and somatic stem cells The role of genetic and epigenetic factors in development
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