bioRxiv · 10.1101/2024.09.19.613945
Morphological profiling in human dopaminergic neurons identifies mitochondrial uncoupling as a neuroprotective effect
Abstract
Parkinsons disease (PD) involves multiple pathological processes in midbrain dopaminergic (mDA) neurons, including protein degradation defects, vesicular trafficking disruption, endolysosomal dysfunction, mitochondrial issues, and oxidative stress. Current PD models often lack complexity and focus on single phenotypes. We used patient-derived SNCA triplication (SNCA-4x) and isogenic control (SNCA-corr) mDA neurons, applying high-content imaging-based morphological profiling to identify and rescue multiple phenotypes. Screening 1,020 compounds, we identified top-scoring compounds that restored healthy profiles in SNCA-4x neurons, increasing Tyrosine hydroxylase (TH) and decreasing -synuclein (Syn) levels. Several hits were linked to mitochondrial biology. Tyrphostin A9, a mitochondrial uncoupler, and several of its structural analogues decreased ROS levels, normalized mitochondrial membrane potential, and increased respiration. Western blotting confirmed that Tyrphostin A9 reduces Syn levels. Our study highlights the neuroprotective potential of mild mitochondrial uncoupling in mDA neurons.
Source connections
Explore related subjects
Keep this discovery
Explore connections, maps & timelines
Gorgogietas, V., Weiss, A., Cousin, L., Hoffmann, D., Schmitt, K., Ogier, A., Barbuti, P. A., Santos, B. F. R., Boussaad, I., Wittich, A., Zaliani, A., Pless, O., Krueger, R., Sommer, P., Wilbertz, J. H.. 2024-09-20. Morphological profiling in human dopaminergic neurons identifies mitochondrial uncoupling as a neuroprotective effect. https://doi.org/10.1101/2024.09.19.613945
Cite the original work for its findings. Save a collection to share your selection of sources.