National Heart and Lung Institute, Imperial College London, London, United Kingdom.
Department of Cardiology, Leiden University Medical Center, Leiden, The Netherlands.
FASEB J. 2019 Sep;33(9):10453-10468. doi: 10.1096/fj.201802740RR. Epub 2019 Jul 5.
Healthy cardiomyocytes are electrically coupled at the intercalated discs by gap junctions. In infarcted hearts, adverse gap-junctional remodeling occurs in the border zone, where cardiomyocytes are chemically and electrically influenced by myofibroblasts. The physical movement of these contacts remains unquantified. Using scanning ion conductance microscopy, we show that intercellular contacts between cardiomyocytes and myofibroblasts are highly dynamic, mainly owing to the edge dynamics (lamellipodia) of the myofibroblasts. Decreasing the amount of functional connexin-43 (Cx43) at the membrane through Cx43 silencing, suppression of Cx43 trafficking, or hypoxia-induced Cx43 internalization attenuates heterocellular contact dynamism. However, we found decreased dynamism and stabilized membrane contacts when cellular coupling was strengthened using 4-phenylbutyrate (4PB). Fluorescent-dye transfer between cells showed that the extent of functional coupling between the 2 cell types correlated with contact dynamism. Intercellular calcein transfer from myofibroblasts to cardiomyocytes is reduced after myofibroblast-specific Cx43 down-regulation. Conversely, 4PB-treated myofibroblasts increased their functional coupling to cardiomyocytes. Consistent with lamellipodia-mediated contacts, latrunculin-B decreases dynamism, lowers physical communication between heterocellular pairs, and reduces Cx43 intensity in contact regions. Our data show that heterocellular cardiomyocyte-myofibroblast contacts exhibit high dynamism. Therefore, Cx43 is a potential target for prevention of aberrant cardiomyocyte coupling and myofibroblast proliferation in the infarct border zone.-Schultz, F., Swiatlowska, P., Alvarez-Laviada, A., Sanchez-Alonso, J. L., Song, Q., de Vries, A. A. F., Pijnappels, D. A., Ongstad, E., Braga, V. M. M., Entcheva, E., Gourdie, R. G., Miragoli, M., Gorelik, J. Cardiomyocyte-myofibroblast contact dynamism is modulated by connexin-43.
健康的心肌细胞通过缝隙连接在闰盘处电偶联。在梗死心脏中,边缘区的缝隙连接发生不良重塑,心肌细胞受成纤维细胞的化学和电影响。这些接触点的物理运动仍未被量化。我们使用扫描离子电导显微镜发现,心肌细胞和成纤维细胞之间的细胞间接触是高度动态的,主要归因于成纤维细胞的边缘动态(片状伪足)。通过 Cx43 沉默、Cx43 运输抑制或缺氧诱导的 Cx43 内化减少膜上功能性连接蛋白 43(Cx43)的数量,会减弱异细胞接触的动态性。然而,我们发现当使用 4-苯丁酸(4PB)增强细胞间偶联时,接触的动态性降低,膜接触稳定。细胞间荧光染料转移显示两种细胞类型之间的功能偶联程度与接触动态性相关。成纤维细胞特异性 Cx43 下调后,细胞间钙黄绿素从成纤维细胞向心肌细胞的转移减少。相反,4PB 处理的成纤维细胞增加了它们与心肌细胞的功能偶联。与片状伪足介导的接触一致,拉他丁-B 降低了动态性,降低了异细胞对之间的物理通讯,并降低了接触区域的 Cx43 强度。我们的数据表明,异细胞心肌细胞-成纤维细胞接触表现出高动态性。因此,Cx43 是预防梗死边缘区异常心肌细胞偶联和成纤维细胞增殖的潜在靶点。