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
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