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连接蛋白43在骨骼肌成肌细胞中的过表达:与心脏细胞移植的相关性。

Overexpression of connexin 43 in skeletal myoblasts: Relevance to cell transplantation to the heart.

作者信息

Suzuki K, Brand N J, Allen S, Khan M A, Farrell A O, Murtuza B, Oakley R E, Yacoub M H

机构信息

Department of Cardiothoracic Surgery, National Heart and Lung Institute, Imperial College School of Medicine at the Heart Science Centre, Harefield Hospital, Middlesex, United Kingdom.

出版信息

J Thorac Cardiovasc Surg. 2001 Oct;122(4):759-66. doi: 10.1067/mtc.2001.116210.

Abstract

OBJECTIVE

Skeletal myoblast transplantation is a promising strategy for treating end-stage heart failure. One potential problem in the development of functional, synchronously contracting grafts is the degree of intercellular communication between grafted myoblasts and host cardiomyocytes. Thus it is expected that enhancement of intercellular gap junction formation would result in improved efficiency of skeletal myoblast transplantation. In this study we investigated whether myoblasts overexpressing connexin 43, a major cardiac gap junction protein, would enhance this intercellular communication.

METHODS AND RESULTS

L6 rat skeletal myoblast cell lines overexpressing connexin 43 were generated by means of gene transfection and clonal selection. Connexin 43 overexpression of these myoblasts, which continued both in undifferentiated and differentiated states (up to 17-fold greater protein level in comparison with control-transfected myoblasts, as measured with Western blotting), was observed on cell surfaces where gap junctions should exist. Both dye microinjection and scrape loading with fluorescent dyes showed enhancement in intercellular dye transfer between connexin 43-transfected myoblasts compared with that found in control-transfected cells. Morphologically, these myoblasts fused and differentiated into multinucleated myotubes more rapidly, demonstrating a higher level of cellular creatine kinase activity as a marker of myogenic differentiation throughout the culture period compared with that of control-transfected myoblasts.

CONCLUSIONS

We have generated connexin 43-overexpressing skeletal myoblast cell lines that resulted in improved formation of functional intercellular gap junctions, which could be relevant to synchronous contraction of grafted myoblasts in the heart. In addition, these cells demonstrated more rapid differentiation, which would also be advantageous in a graft for transplantation to the heart.

摘要

目的

骨骼肌成肌细胞移植是治疗终末期心力衰竭的一种很有前景的策略。在构建具有功能的、同步收缩的移植物过程中,一个潜在问题是移植的成肌细胞与宿主心肌细胞之间的细胞间通讯程度。因此,预计增强细胞间缝隙连接的形成将提高骨骼肌成肌细胞移植的效率。在本研究中,我们调查了过表达连接蛋白43(一种主要的心脏缝隙连接蛋白)的成肌细胞是否会增强这种细胞间通讯。

方法与结果

通过基因转染和克隆筛选,构建了过表达连接蛋白43的L6大鼠骨骼肌成肌细胞系。这些成肌细胞在未分化和分化状态下均持续过表达连接蛋白43(与对照转染的成肌细胞相比,蛋白质水平通过蛋白质印迹法测定最高可达17倍),在应该存在缝隙连接的细胞表面观察到这种过表达。与对照转染细胞相比,染料微量注射和荧光染料刮擦加载均显示连接蛋白43转染的成肌细胞之间的细胞间染料转移增强。从形态学上看,这些成肌细胞更快地融合并分化为多核肌管,与对照转染的成肌细胞相比,在整个培养期间作为肌源性分化标志物的细胞肌酸激酶活性水平更高。

结论

我们构建了过表达连接蛋白43的骨骼肌成肌细胞系,其导致功能性细胞间缝隙连接形成改善,这可能与移植到心脏中的成肌细胞的同步收缩有关。此外,这些细胞表现出更快的分化,这在移植到心脏的移植物中也将是有利的。

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