College of Life Sciences, Qufu Normal University, Qufu, Shandong, China.
Exp Physiol. 2023 Sep;108(9):1189-1202. doi: 10.1113/EP090518. Epub 2023 Aug 11.
Long-term weightlessness in animals can cause changes in myocardial structure and function, in which mitochondria play an important role. Here, a tail suspension (TS) Kunming mouse (Mus musculus) model was used to simulate the effects of weightlessness on the heart. We investigated the effects of 2 and 4 weeks of TS (TS2 and TS4) on myocardial mitochondrial ultrastructure and oxidative respiratory function and on the molecular mechanisms of apoptosis and mitochondrial fission, autophagy and fusion-related signalling. Our study revealed significant changes in the ultrastructural features of cardiomyocytes in response to TS. The results showed: (1) mitochondrial swelling and disruption of cristae in TS2, but mitochondrial recovery and denser cristae in TS4; (2) an increase in the total number of mitochondria and number of sub-mitochondria in TS4; (3) no significant changes in the nuclear ultrastructure or DNA fragmentation among the two TS groups and the control group; (4) an increase in the bax/bcl-2 protein levels in the two TS groups, indicating increased activation of the bax-mediated apoptosis pathway; (5) no change in the phosphorylation ratio of dynamin-related protein 1 in the two TS groups; (6) an increase in the protein levels of optic atrophy 1 and mitofusin 2 in the two TS groups; and (7) in comparison to the TS2 group, an increase in the phosphorylation ratio of parkin and the ratio of LC3II to LC3I in TS4, suggesting an increase in autophagy. Taken together, these findings suggest that mitochondrial autophagy and fusion levels increased after 4 weeks of TS, leading to a restoration of the bax-mediated myocardial apoptosis pathway observed after 2 weeks of TS. NEW FINDINGS: What is the central question of this study? What are the effects of 2 and 4 weeks of tail suspension on myocardial mitochondrial ultrastructure and oxidative respiratory function and on the molecular mechanisms of apoptosis and mitochondrial fission, autophagy and fusion-related signalling? What is the main finding and its importance? Increased mitochondrial autophagy and fusion levels after 4 weeks of tail suspension help to reshape the morphology and increase the number of myocardial mitochondria.
长期失重会导致动物心肌结构和功能发生变化,其中线粒体起着重要作用。本研究采用尾部悬吊(tail suspension,TS)昆明小鼠模型模拟失重对心脏的影响。我们研究了 2 周和 4 周 TS(TS2 和 TS4)对心肌线粒体超微结构和氧化呼吸功能的影响,以及凋亡和线粒体分裂、自噬和融合相关信号通路的分子机制。研究发现,TS 后心肌细胞超微结构特征发生明显变化:(1)TS2 中线粒体肿胀,嵴断裂,而 TS4 中线粒体恢复,嵴更密集;(2)TS4 中线粒体数量和亚线粒体数量增多;(3)2 个 TS 组和对照组之间,核超微结构或 DNA 片段均无明显变化;(4)2 个 TS 组 bax/bcl-2 蛋白水平升高,表明 bax 介导的凋亡途径激活增加;(5)2 个 TS 组 dynamin-related protein 1 磷酸化比例无变化;(6)2 个 TS 组 optic atrophy 1 和 mitofusin 2 蛋白水平升高;(7)与 TS2 组相比,TS4 组 parkin 磷酸化比例和 LC3II/LC3I 比值增加,提示自噬增加。综上,4 周 TS 后线粒体自噬和融合水平增加,恢复了 2 周 TS 后 bax 介导的心肌凋亡途径。