Ischaemia impacts TNT-mediated communication between cardiac cells

Daniela Batista-Almeida , Teresa Ribeiro-Rodrigues , Tânia Martins-Marques , Luisa Cortes , Manuel J. Antunes , Pedro E. Antunes , Lino Gonçalves , Christel Brou , Trond Aasen , Chiara Zurzolo , Henrique Girão
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引用次数: 7

Abstract

Efficient contraction of the heart relies on a highly regulated communication network between cardiac cells. Direct intercellular communication is mediated by gap junctions but can also occur through tubular structures named tunnelling nanotubes (TNTs), which connect the cytoplasm of neighbouring cells and facilitate the transport of various cargoes. Although the formation of TNTs between cardiomyocytes has been reported, the effect of ischaemia on this process remains unclear. In this work, we assessed the impact of ischaemia and oxidative stress on TNT-mediated communication between cardiac cells. We found that cardiac cell lines and neonatal primary cultures of cardiomyocytes subjected to in vitro ischaemia form more TNTs than control cells. Moreover, antioxidants prevented ischaemia-induced TNT formation, suggesting that oxidative stress regulates this process. Furthermore, we identified troponin T as a new specific marker of cardiomyocyte-derived TNTs, which allows for the identification of heterocellular TNT connections between cardiomyocytes and other resident cells in the heart, such as fibroblasts. We also determined the presence of TNT-like structures in rat and human hearts. Rat hearts subjected to global ischaemia in the ex vivo Langendorff system showed increased formation of TNTs. Altogether, this study demonstrates that ischaemia affects the formation of TNTs in the heart and sheds new light on the regulation of TNT-mediated communication between cardiomyocytes.

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缺血影响心肌细胞间tnt介导的通讯
心脏的有效收缩依赖于心脏细胞之间高度调节的通信网络。直接的细胞间通讯是由间隙连接介导的,但也可以通过称为隧道纳米管(TNTs)的管状结构发生,它连接邻近细胞的细胞质并促进各种货物的运输。尽管已经报道了心肌细胞之间形成tnt,但缺血对这一过程的影响尚不清楚。在这项工作中,我们评估了缺血和氧化应激对心肌细胞间tnt介导的通讯的影响。我们发现心脏细胞系和新生儿心肌细胞原代培养物在体外缺血时形成的tnt比对照细胞多。此外,抗氧化剂阻止了缺血诱导的TNT形成,这表明氧化应激调节了这一过程。此外,我们发现肌钙蛋白T是心肌细胞来源的TNT的一种新的特异性标记物,它允许鉴定心肌细胞和心脏中其他常驻细胞(如成纤维细胞)之间的异细胞TNT连接。我们还确定了大鼠和人类心脏中存在类似tnt的结构。在体外Langendorff系统中,遭受全局缺血的大鼠心脏显示tnt的形成增加。总之,这项研究表明,缺血影响心脏中tnt的形成,并为tnt介导的心肌细胞间通讯的调节提供了新的思路。
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