Differential ROS-Mediated Phosphorylation of Drp1 in Mitochondrial Fragmentation Induced by Distinct Cell Death Conditions in Cerebellar Granule Neurons

<div>Role of mtROS in the viability of CGN treated with K5 and ST. Cell viability was evaluated by MTT reduction after 24 h of death induction in cells pretreated for 30 min with the mitochondrial antioxidant MitoTEMPO (10 <i>μ</i>M). (a) Viability of CGN treated with K5. (b) Viability of CGN treated with ST. 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Oxidative Medicine and Cellular Longevity

fig3

Figure 3

Figure 3: Differential ROS-Mediated Phosphorylation of Drp1 in Mitochondrial Fragmentation Induced by Distinct Cell Death Conditions in Cerebellar Granule Neurons 

Figure 3 | Differential ROS-Mediated Phosphorylation of Drp1 in Mitochondrial Fragmentation Induced by Distinct Cell Death Conditions in Cerebellar Granule Neurons 