Department of Integrative and Systems Physiology, Faculty of Medical Sciences, University of Fukui, Fukui 910-1193, Japan.
Life Science Innovation Center, University of Fukui, Fukui 910-1193, Japan.
Int J Mol Sci. 2022 Jul 19;23(14):7948. doi: 10.3390/ijms23147948.
The mitochondrial Na-Ca exchanger, NCLX, was reported to supply Ca to sarcoplasmic reticulum (SR)/endoplasmic reticulum, thereby modulating various cellular functions such as the rhythmicity of cardiomyocytes, and cellular Ca signaling upon antigen receptor stimulation and chemotaxis in B lymphocytes; however, there is little information on the spatial relationships of NCLX with SR Ca handling proteins, and their physiological impact. Here we examined the issue, focusing on the interaction of NCLX with an SR Ca pump SERCA in cardiomyocytes. A bimolecular fluorescence complementation assay using HEK293 cells revealed that the exogenously expressed NCLX was localized in close proximity to four exogenously expressed SERCA isoforms. Immunofluorescence analyses of isolated ventricular myocytes showed that the NCLX was localized to the edges of the mitochondria, forming a striped pattern. The co-localization coefficients in the super-resolution images were higher for NCLX-SERCA2, than for NCLX-ryanodine receptor and NCLX-Na/K ATPase α-1 subunit, confirming the close localization of endogenous NCLX and SERCA2 in cardiomyocytes. The mathematical model implemented with the spatial and functional coupling of NCLX and SERCA well reproduced the NCLX inhibition-mediated modulations of SR Ca reuptake in HL-1 cardiomyocytes. Taken together, these results indicated that NCLX and SERCA are spatially and functionally coupled in cardiomyocytes.
线粒体 Na-Ca 交换器(NCLX)被报道能向肌浆网(SR)/内质网供应 Ca,从而调节各种细胞功能,如心肌细胞的节律性、抗原受体刺激和 B 淋巴细胞趋化性时的细胞内 Ca 信号;然而,关于 NCLX 与 SR Ca 处理蛋白的空间关系及其生理影响的信息却很少。本文聚焦于心肌细胞中 NCLX 与 SR Ca 泵 SERCA 的相互作用,对此问题进行了研究。使用 HEK293 细胞的双分子荧光互补测定显示,外源性表达的 NCLX 定位于四个外源性表达的 SERCA 同工型附近。分离的心室肌细胞的免疫荧光分析显示,NCLX 定位于线粒体的边缘,形成条纹状图案。超分辨率图像中的共定位系数对于 NCLX-SERCA2 高于 NCLX-ryanodine 受体和 NCLX-Na/K ATPase α-1 亚基,证实了内源性 NCLX 和 SERCA2 在心肌细胞中的紧密定位。用 NCLX 和 SERCA 的空间和功能偶联实现的数学模型很好地再现了 NCLX 抑制介导的 HL-1 心肌细胞中 SR Ca 重摄取的调制。总之,这些结果表明 NCLX 和 SERCA 在心肌细胞中空间上和功能上是偶联的。