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Macroautophagy-gene...
Macroautophagy-generated increase of lysosomal amyloid β-protein mediates oxidant-induced apoptosis of cultured neuroblastoma cells
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- Zheng, Lin (författare)
- Linköpings universitet,Geriatrik,Hälsouniversitetet
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- Terman, Alexi (författare)
- Karolinska Institutet,Karolinska University Hospital, Stockholm
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- Hallbeck, Martin (författare)
- Östergötlands Läns Landsting,Linköpings universitet,Experimentell patologi,Hälsouniversitetet,Klinisk patologi och klinisk genetik
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- Dehvari, Nodi (författare)
- Karolinska Institutet, Stockholm
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- Cowburn, Richard F. (författare)
- Karolinska Institutet,AstraZeneca, Södertälje
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- Benedikz, Eirikur (författare)
- Karolinska Institutet
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- Kågedal, Katarina (författare)
- Linköpings universitet,Experimentell patologi,Hälsouniversitetet
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- Cedazo-Minguez, Angel (författare)
- Karolinska Institutet
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- Marcusson, Jan (författare)
- Östergötlands Läns Landsting,Linköpings universitet,Geriatrik,Hälsouniversitetet,Geriatriska kliniken
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(creator_code:org_t)
- 2014-10-28
- 2011
- Engelska.
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Ingår i: Autophagy. - : Landes Bioscience. - 1554-8627 .- 1554-8635. ; 7:12, s. 1528-1545
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https://doi.org/10.4...
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Abstract
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- Increasing evidence suggests the toxicity of intracellular amyloid β-protein (Aβ) to neurons, as well as the involvement of oxidative stress in Alzheimer disease (AD). Here we show that normobaric hyperoxia (exposure of cells to 40% oxygen for five days, and consequent activation of macroautophagy and accumulation of Aβ within lysosomes, induced apoptosis in differentiated SH-SY5Y neuroblastoma cells. Cells under hyperoxia showed: (1) increased numbers of autophagic vacuoles that contained amyloid precursor protein (APP) as well as Aβ monomers and oligomers, (2) increased reactive oxygen species production, and (3) enhanced apoptosis. Oxidant-induced apoptosis positively correlated with cellular Aβ production, being the highest in cells that were stably transfected with APP Swedish KM670/671NL double mutation. Inhibition of γ-secretase, prior and/or in parallel to hyperoxia, suggested that the increase of lysosomal Aβ resulted mainly from its autophagic uptake, but also from APP processing within autophagic vacuoles. The oxidative stress-mediated effects were prevented by macroautophagy inhibition using 3-methyladenine or ATG5 downregulation. Our results suggest that upregulation of macroautophagy and resulting lysosomal Aβ accumulation are essential for oxidant-induced apoptosis in cultured neuroblastoma cells and provide aditional support for the interactive role of oxidative stress and the lysosomal system in AD-related neurodegeneration.
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