Elevated caspase 3 activity and cytosolic cytochrome c in NT2 cybrids containing amyotrophic lateral sclerosis subject mtDNA. (1st September 2016)

• Record Type: Journal Article
• Authors: Shrivastava, Mohita; Subbiah, Vivekanandhan
• Is Part Of: International journal of neuroscience. Volume 126:Number 9(2016:Sep.)
• Page Start: 839
• Page End: 849
• Publication Date: 2016-09-01
• Subjects: ALS -- cybrids -- apoptosis -- cytochrome c -- caspases; Nervous system -- Periodicals; 612.805
• DOI: 10.3109/00207454.2015.1074902
• Languages: English
• ISSNs: 0020-7454

Abstract

Abstract : Apoptosis of motor neurons is an important feature in amyotrophic lateral sclerosis (ALS). A vital role of mitochondria in apoptosis and cell survival is well documented. Eventually mitochondria have shown to be an early target in the pathogenesis of ALS. On account of these facts, we investigated the involvement of mitochondrial-dependent apoptosis in ALS and control (CTR) cybrids, generated fusing human platelets with mitochondrial DNA-depleted NT2-neuroteratocarcinoma cells. After a 6 week selection process during which transferred subject mtDNA repopulated the NT2 cells and restored mitochondrial oxygen consumption, we assessed cell viability and two programmed cell death parameters, caspase 3 activity and cytosolic cytochrome c levels. Compared to the control cybrid lines ( n = 5), the ALS cybrid lines ( n = 10) showed 45% less XTT reduction and higher caspase 3 activity ( p < 0.05, two-way Student's t test) exhibiting lesser cell viability and execution of apoptosis. Elevated cytosolic cytochrome c levels in ALS cybrid lines ( n = 8) than in CTR ( n = 4) ( p < 0.05, two-way Student's t -test) indicating its mitochondrial release and initiation of apoptosis. This indicates apoptosis as one of the possible mechanisms of cell death in ALS. Our findings support the view that in ALS, subject's mitochondria are altered in non-degenerating tissues in such a way that intrinsic apoptotic pathway activity is relatively increased.