| Literature DB >> 30350549 |
Qixin Chen1,2,3, Chengzhi Jin4, Xintian Shao1,2,3, Ruilin Guan4, Zhiqi Tian1, Chenran Wang1, Fei Liu2,3, Peixue Ling2,3, Jun-Lin Guan1, Liangnian Ji4, Fengshan Wang2, Hui Chao4, Jiajie Diao1.
Abstract
Combining luminescent transition metal complex with super-resolution microscopy is an excellent strategy for the long-term visualization of the dynamics of subcellular structures in living cells. However, it remains unclear whether iridium(III) complexes are applicable for a particular type of super-resolution technique, structured illumination microscopy (SIM), to image subcellular structures. Herein, an iridium(III) dye, to track mitochondrial dynamics in living cells under SIM is described. The dye demonstrates excellent specificity and photostability and satisfactory cell permeability. While using SIM to image mitochondria, an ≈80 nm resolution is achieved that allows the clear observation of the structure of mitochondrial cristae. The dye is used to monitor and quantify mitochondrial dynamics relative to lysosomes, including fusion involved in mitophagy, and newly discovered mitochondria-lysosome contact (MLC) under different conditions. The MLC remains intact and fusion vanishes when five receptors, p62, NDP52, OPTN, NBR1, and TAX1BP1, are knocked out, suggesting that these two processes are independent.Entities:
Keywords: iridium(III) luminophore; mitochondrial dynamic; structured illumination microscopy
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Year: 2018 PMID: 30350549 DOI: 10.1002/smll.201802166
Source DB: PubMed Journal: Small ISSN: 1613-6810 Impact factor: 13.281