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Sökning: id:"swepub:oai:DiVA.org:umu-157037" > The molecular patho...

The molecular pathogenesis of superoxide dismutase 1-linked ALS is promoted by low oxygen tension

Keskin, Isil, 1987- (författare)
Umeå universitet,Patologi
Forsgren, Elin (författare)
Umeå universitet,Klinisk neurovetenskap
Lehmann, Manuela (författare)
Umeå universitet,Klinisk neurovetenskap
visa fler...
Andersen, Peter M. (författare)
Umeå universitet,Klinisk neurovetenskap
Brännström, Thomas (författare)
Umeå universitet,Patologi
Lange, Dale J. (författare)
Synofzik, Matthis (författare)
Nordström, Ulrika (författare)
Umeå universitet,Klinisk neurovetenskap
Zetterström, Per (författare)
Umeå universitet,Klinisk kemi
Marklund, Stefan L. (författare)
Umeå universitet,Klinisk kemi
Gilthorpe, Jonathan D. (författare)
Umeå universitet,Klinisk neurovetenskap
visa färre...
 (creator_code:org_t)
2019-03-12
2019
Engelska.
Ingår i: Acta Neuropathologica. - New York : Springer. - 0001-6322 .- 1432-0533. ; 138:1, s. 85-101
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Mutations in superoxide dismutase 1 (SOD1) cause amyotrophic lateral sclerosis (ALS). Disease pathogenesis is linked to destabilization, disorder and aggregation of the SOD1 protein. However, the non-genetic factors that promote disorder and the subsequent aggregation of SOD1 have not been studied. Mainly located to the reducing cytosol, mature SOD1 contains an oxidized disulfide bond that is important for its stability. Since O2 is required for formation of the bond, we reasoned that low O2 tension might be a risk factor for the pathological changes associated with ALS development. By combining biochemical approaches in an extensive range of genetically distinct patient-derived cell lines, we show that the disulfide bond is an Achilles heel of the SOD1 protein. Culture of patient-derived fibroblasts, astrocytes, and induced pluripotent stem cell-derived mixed motor neuron and astrocyte cultures (MNACs) under low oxygen tensions caused reductive bond cleavage and increases in disordered SOD1. The effects were greatest in cells derived from patients carrying ALS-linked mutations in SOD1. However, significant increases also occurred in wild-type SOD1 in cultures derived from non-disease controls, and patients carrying mutations in other common ALS-linked genes. Compared to fibroblasts, MNACs showed far greater increases in SOD1 disorder and even aggregation of mutant SOD1s, in line with the vulnerability of the motor system to SOD1-mediated neurotoxicity. Our results show for the first time that O2 tension is a principal determinant of SOD1 stability in human patient-derived cells. Furthermore, we provide a mechanism by which non-genetic risk factors for ALS, such as aging and other conditions causing reduced vascular perfusion, could promote disease initiation and progression.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Amyotrophic lateral sclerosis (ALS)
Superoxide dismutase 1 (SOD1)
Disulfide bond
Oxygen tension
Protein disorder
Protein aggregation
Patient-derived cells

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