在共培养模型中骨髓细胞与离体大鼠心肌细胞间细胞间连接的形成

J. Skopalík, M. Pásek, Milan Rychtarik, Z. Kořístek, E. Gabrielova, P. Scheer, P. Matejovič, M. Modriansky, M. Klabusay
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引用次数: 5

摘要

目的:心肌细胞有限的再生潜能导致心脏组织在病理过程中发生不可逆的变化。然而,骨髓单核细胞(BM-MNCs)可以迁移到该组织,融入死亡或缺失的肌细胞区域,并改善整体心脏功能。BMMSCs与CMs结合及相互作用的机制尚不清楚。我们的目标是建立一个体外模型,以研究BM-MNCs与CMs的相互作用,并对这些相互作用进行显微镜描述。方法与结果:从成年大鼠和新生大鼠中分离CMs。BM-MNCs从骨髓中分离。在肌细胞培养中加入BM-MNCs。通过荧光显微镜评估细胞间粘附和Cx43的表达,通过荧光测量在电刺激下心肌细胞- bmc通信中的Ca2+瞬变。利用荧光显微镜分析钙黄蛋白从BM-MNCs到CMs的转运。结论:BM-MNCs对CMs的粘附速度快且稳定。在BM-MNCs与cm的接触区检测到Cx43;在共培养的所有bm - mnc -心肌细胞对中,显示Cx43阳性的对占不到1%。CMs和BM-MNCs之间形成导电结构,并通过成像钙黄蛋白转移和同步Ca2+瞬态来验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formation of Cell-To-Cell Connection between Bone Marrow Cells and Isolated Rat Cardiomyocytes in a Cocultivation Model
Aims: Limited regenerative potential of cardiomyocytes (CMs) causes irreversible changes in heart tissue during pathological processes. However bone marrow mononuclear cells (BM-MNCs) can migrate to this tissue, incorporate to the area of dead or missing myocytes, and improve the global heart function. The mechanism of BMMSCs’ incorporation and interaction with CMs is not clear. Our aim was to create an in vitro model which would enable to study the interaction of BM-MNCs with CMs and to make a microscopy description of these interactions. Methods and Results: CMs were isolated from adult and newborn rats. BM-MNCs were isolated from bone marrow. BM-MNCs were added to the myocyte culture. Cell-to-cell adherence and Cx43 expression were evaluated by fluorescence microscopy, Ca2+ transients were evaluated in cardiomyocyte-BMC communication under electrical stimulation by fluo-4 fluorescence measurement. Analysis of calcein transport from BM-MNCs to CMs was performed using fluorescence microscopy. Conclusions: The adherence of BM-MNCs to CMs occurred quickly and was stable. Cx43 was detected in contact zones between BM-MNCs and CMs; pairs which displayed Cx43 positivity represented less than 1% from all BM-MNC-cardiomyocyte pairs in the coculture. Conductive structures between CMs and BM-MNCs were formed and verified by imaging calcein transfer and synchronous Ca2+ transients.
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