Imaging of mitochondria/lysosomes in live cells and

Two rhodamine-phenothiazine conjugates, RP1 and RP2 , were synthesized, and their photophysical properties, subcellular localization, and photocytotoxicity were investigated. We observed robust localization of RP1 in mitochondria and dual localization in mitochondria and lysosomes with RP2 in live c...

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Bibliographic Details
Published inOrganic & biomolecular chemistry Vol. 21; no. 1; pp. 222 - 2231
Main Authors Singh, Deepmala, Regar, Ramprasad, Soppina, Pushpanjali, Soppina, Virupakshi, Kanvah, Sriram
Format Journal Article
Published 08.03.2023
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Summary:Two rhodamine-phenothiazine conjugates, RP1 and RP2 , were synthesized, and their photophysical properties, subcellular localization, and photocytotoxicity were investigated. We observed robust localization of RP1 in mitochondria and dual localization in mitochondria and lysosomes with RP2 in live cells. Live cell imaging with these probes allowed us to track the dynamics of mitochondria and lysosomes during ROS-induced mitochondrial damage and the subsequent lysosomal digestion of the damaged mitochondria. The fluorophores also demonstrated preferential accumulation in cancer cells compared to normal cells and had strong photo-cytotoxicity. However, no cytotoxicity was observed in the dark. The mitochondrial staining and light-induced ROS production were not limited to mammalian cell lines, but were also observed in the animal model C. elegans . The study demonstrated the potential applications of these probes in visualizing the mitochondria-lysosome cross-talk after ROS production and for photodynamic therapy. ROS-mediated cross-talk between mitochondria and lysosomes can be visualized using rhodamine-phenothiazine conjugates.
Bibliography:Electronic supplementary information (ESI) available: Fig. S1-S6, Videos S1 and S2; characterisation spectral data of the synthesized compounds. See DOI
https://doi.org/10.1039/d3ob00086a
ISSN:1477-0520
1477-0539
DOI:10.1039/d3ob00086a