Super-resolution quantification of nanoscale damage to mitochondria in live cells

被引:0
|
作者
Xintian Shao
Qixin Chen
Lianting Hu
Zhiqi Tian
Liuyi Liu
Fei Liu
Fengshan Wang
Peixue Ling
Zong-Wan Mao
Jiajie Diao
机构
[1] National-Local Joint Engineering Laboratory of Polysaccharide Drugs,Shandong Academy of Pharmaceutical Sciences, Key Laboratory of Biopharmaceuticals, Engineering Laboratory of Polysaccharide Drugs
[2] University of Cincinnati College of Medicine,Department of Cancer Biology
[3] Shandong University,School of Pharmaceutical Sciences, Cheeloo College of Medicine
[4] Shandong First Medical University & Shandong Academy of Medical Sciences,School of Information Management
[5] Wuhan University,MOE Key Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry
[6] Sun Yat-Sen University,undefined
来源
Nano Research | 2020年 / 13卷
关键词
mitochondria; structured illumination microscopy; quantification analyze; morphology; cristae;
D O I
暂无
中图分类号
学科分类号
摘要
Mitochondrial damage, characterized by altered morphological distribution and the damage of cristae, is closely associated with mitochondrial disease. However, imaging methods for capturing mitochondrial morphology at the nanoscale level in live samples remain unavailable, which seriously hinders the accurate evaluation and diagnosis of mitochondrial-related diseases. In response, we propose a super-resolution quantification strategy based on structured illumination microscopy (SIM) for the rapid, accurate evaluation of mitochondrial morphology. Using the strategy, we accurately captured the morphological distribution of mitochondria at the nanoscale level in a way generally applicable to checking various cell processes and identifying patients with mitochondrial disease who exhibit the SLC25A46 mutation. We also used algorithm-assisted super-resolution imaging to quantitatively analyze damage to mitochondrial cristae, which supports a novel drug screening strategy—high-resolution drug screening—for investigating drugs’ pharmacodynamics on organelles in living cells. In short, our strategy improves the accurate examination of changes in mitochondrial morphology in living cells and indicates new ways in which SIM-imaging can assist in diagnosing mitochondrial disease at the single-cell level.
引用
收藏
页码:2149 / 2155
页数:6
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