Wang Lei, Chen Rui, Han Guanqun, Liu Xuan, Huang Taosheng, Diao Jiajie, Sun Yujie
Department of Cancer Biology, College of Medicine, University of Cincinnati, Cincinnati, OH 45267, USA.
Department of Chemistry, University of Cincinnati, Cincinnati, OH 45221, USA.
Exploration (Beijing). 2022 Jun;2(3). doi: 10.1002/exp.20210215. Epub 2022 Mar 22.
Lysosomes are multifunctional organelles involved in macromolecule degradation, nutrient sensing and autophagy. Live imaging has revealed lysosome subpopulations with dynamics and characteristic cellular localization. An as-yet unanswered question is whether lysosomes are spatially organized to coordinate and integrate their functions. Combined with super-resolution microscopy, we designed a small organic fluorescent probe, TPAE, that targeted lysosomes with a large Stokes shift. When we analyzed the spatial organization of lysosomes against mitochondria in different cell lines with this probe, we discovered different distance distribution patterns between lysosomes and mitochondria during increased autophagy flux. By using mutation fibroblasts derived from patients containing highly fused mitochondria with low oxidative phosphorylation, we concluded that unhealthy mitochondria redistributed the subcellular localization of lysosomes, which implies a strong connection between mitochondria and lysosomes.
溶酶体是参与大分子降解、营养感知和自噬的多功能细胞器。实时成像揭示了具有动态变化和特征性细胞定位的溶酶体亚群。一个尚未得到解答的问题是,溶酶体是否在空间上进行组织以协调和整合其功能。结合超分辨率显微镜,我们设计了一种小型有机荧光探针TPAE,它以大斯托克斯位移靶向溶酶体。当我们用该探针分析不同细胞系中溶酶体与线粒体的空间组织时,我们发现在自噬通量增加期间,溶酶体与线粒体之间存在不同的距离分布模式。通过使用来自含有高度融合线粒体且氧化磷酸化水平低的患者的突变成纤维细胞,我们得出结论,不健康的线粒体重新分布了溶酶体的亚细胞定位,这意味着线粒体与溶酶体之间存在紧密联系。