Methods for mitochondrial health assessment by High Content Imaging System
1
Issued Date
2022-01-01
Resource Type
eISSN
22150161
Scopus ID
2-s2.0-85128292515
Journal Title
MethodsX
Volume
9
Rights Holder(s)
SCOPUS
Bibliographic Citation
MethodsX Vol.9 (2022)
Suggested Citation
Panusatid C., Thangsiriskul N., Peerapittayamongkol C. Methods for mitochondrial health assessment by High Content Imaging System. MethodsX Vol.9 (2022). doi:10.1016/j.mex.2022.101685 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/84822
Title
Methods for mitochondrial health assessment by High Content Imaging System
Author's Affiliation
Other Contributor(s)
Abstract
Mitochondria are important organelles responsible for energy production. Mitochondrial dysfunction relates to various pathological diseases. The investigation of mitochondrial heath is critical to evaluate the cellular status. Herein, we demonstrated an approach for determining the status of mitochondrial health by observing mitochondrial H2O2 (one type of ROS), membrane potential, and morphology (fragmentation and length) in live primary fibroblast cells. The cells were co-stained with fluorescent dyes (Hoechst 33342 and MITO-ID® Red/MitoPY1/JC-10) and continuously processed by the High Content Imaging System. We employed the Operetta CLSTM to take fluorescent images with its given quickness and high resolution. The CellProfiler image analysis software was further used to identify cell and mitochondrial phenotypes in the thousand fluorescent images. • We could quantitatively analyze fluorescent images with high-throughput and high-speed detection to track the alteration of mitochondrial status. • The MMP assay is sensitive to FCCP even at the concentration of 0.01 µM. • The fibroblast cells treated with stress inducers (H2O2, FCCP, and phenanthroline) revealed a significant change in mitochondrial health parameters, with more ROS accumulation, depolarized MMP, increased fragmentation, and reduced length of mitochondria.