A high-throughput real-time in vitro assay using mitochondrial targeted roGFP for screening of drugs targeting mitochondria
Autor: | Pramod Darvin, Prakash Rajappan Pillai, Asha Lekshmi, Aneesh Chandrasekharan, M. Radhakrishna Pillai, Santhik Subhasingh Lupitha, Leena Chandrasekhar, T.R. Santhoshkumar, Shankara Narayanan Varadarajan |
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Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
NA Numerical Aperture Clinical Biochemistry Gene Expression TMRM Tetramethyl-rhodamine Methyl Ester Apoptosis Mitochondrion FRET Förster Resonance Energy Transfer HyPer-red Red fluorescence-based hydrogen peroxide sensor Biochemistry IMS-RP Inter-Membrane Space Reporter Protein RoGFP 0302 clinical medicine Genes Reporter Drug Discovery Cytotoxicity lcsh:QH301-705.5 bcl-2-Associated X Protein lcsh:R5-920 Microscopy Confocal Smac Second mitochondria-derived activator of caspases Chemistry Cytochromes c H2B-mCherry Histone 2B-mCherry EGCG EpiGalloCatechin Gallate Mitochondria Molecular Imaging Cell biology Drug screening mt-roGFP mitochondrial targeted reduction-oxidation sensitive Green Fluorescent Protein2 Mitochondrial oxidation HTS High-Throughput Screening RPMI 1640 Roswell Park Memorial Institute 1640 lcsh:Medicine (General) Oxidation-Reduction Research Paper Programmed cell death Cell signaling Green Fluorescent Proteins EGFP Enhanced Green Fluorescent Protein DMEM Dulbecco's Modified Eagle Medium 17AAG 17-(Allylamino)-17-demethoxygeldanamycin 03 medical and health sciences Cell Line Tumor medicine Humans roGFP Organic Chemistry Cancer medicine.disease In vitro High-Throughput Screening Assays 030104 developmental biology lcsh:Biology (General) rxYFP redox-sensitive Yellow Fluorescent Protein Reactive Oxygen Species 030217 neurology & neurosurgery |
Zdroj: | Redox Biology, Vol 20, Iss, Pp 379-389 (2019) Redox Biology |
ISSN: | 2213-2317 |
Popis: | Most toxic compounds including cancer drugs target mitochondria culminating in its permeabilization. Cancer drug-screening and toxicological testing of compounds require cost-effective and sensitive high-throughput methods to detect mitochondrial damage. Real-time methods for detection of mitochondrial damage are less toxic, allow kinetic measurements with good spatial resolution and are preferred over end-stage assays. Cancer cell lines stably expressing genetically encoded mitochondrial-targeted redox-GFP2 (mt-roGFP) were developed and validated for its suitability as a mitochondrial damage sensor. Diverse imaging platforms and flow-cytometry were utilized for ratiometric analysis of redox changes with known toxic and cancer drugs. Key events of cell death and mitochondrial damage were studied at single-cell level coupled with mt-roGFP. Cells stably expressing mt-roGFP and H2B-mCherry were developed for high-throughput screening (HTS) application. Most cancer drugs while inducing mitochondrial permeabilization trigger mitochondrial-oxidation that can be detected at single-cell level with mt-roGFP. The image-based assay using mt-roGFP outperformed other quantitative methods of apoptosis in ease of screening. Incorporation of H2B-mCherry ensures accurate and complete automated segmentation with excellent Z value. The results substantiate that most cancer drugs and known plant-derived antioxidants trigger cell-death through mitochondrial redox alterations with pronounced ratio change in the mt-roGFP probe. Real-time analysis of mitochondrial oxidation and mitochondrial permeabilization reveal a biphasic ratio change in dying cells, with an initial redox surge before mitochondrial permeabilization followed by a drastic increase in ratio after complete mitochondrial permeabilization. Overall, the results prove that mitochondrial oxidation is a reliable indicator of mitochondrial damage, which can be readily determined in live cells using mt-roGFP employing diverse imaging techniques. The assay described is highly sensitive, easy to adapt to HTS platforms and is a valuable resource for identifying cytotoxic agents that target mitochondria and also for dissecting cell signaling events relevant to redox biology. Highlights • Mitochondrial oxidation is an universal marker for mitochondrial damage and mitochondrial permeabilization. • Ratiometric imaging of mt-roGFP in high-throughput mode allows rapid screening of compounds that target mitochondria. • Real-time ratiometric imaging of mt-roGFP and mitochondrial permeabilization reveals a biphasic redox alteration in cells undergoing mitochondrial permeabilization. |
Databáze: | OpenAIRE |
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