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Superoxide dismutase in CSF from amyotrophic lateral sclerosis patients with and without CuZn-superoxide dismutase mutations

Jacobsson, Johan (author)
Umeå universitet,Klinisk neurovetenskap
Jonsson, Andreas P. (author)
Umeå universitet,Klinisk kemi
Andersen, Peter M. (author)
Umeå universitet,Klinisk neurovetenskap
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Forsgren, Lars (author)
Umeå universitet,Klinisk neurovetenskap
Marklund, Stefan L. (author)
Umeå universitet,Klinisk kemi
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 (creator_code:org_t)
Oxford University Press, 2001
2001
English.
In: Brain. - : Oxford University Press. - 0006-8950 .- 1460-2156. ; 124:7, s. 1461-1466
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Mutations in CuZn-superoxide dismutase (CuZn-SOD) have been linked to familial amyotrophic lateral sclerosis (ALS), and motor neurone death is caused by the gain of a toxic property of the mutant protein. Here we determined amounts, activity and molecular forms of CuZn-SOD in CSF from ALS patients carrying the D90A and other CuZn-SOD mutations and patients without such mutations. There were no differences in amount of protein and enzymic activities of CuZn-SOD between 37 neurological controls, 54 sporadic and 12 familial ALS cases, and 10 cases homozygous for the D90A mutation. Three cases heterozygous for the A89V, S105L and G114A CuZn-SOD mutations showed low amounts of CuZn-SOD. There was no evidence for accumulation of inactive protein in any of the groups. Immunoblots showed no evidence for the presence of any precipitates or other molecular forms of CuZn-SOD with higher molecular weight in the groups. About 25% of the CuZn-SOD subunits in CSF from controls shows an N-terminal truncation. This truncated portion does not differ between controls and ALS groups not carrying CuZn-SOD mutations, but is 70% larger in samples from D90A homozygous ALS patients. The findings suggest an essentially normal amount and activity of D90A mutant CuZn-SOD in CNS tissues of ALS cases. The increased occurrence of N-terminally truncated mutant subunits may indicate a difference in degradation routes compared with the wild-type enzyme, resistance against subsequent proteolytic steps and/or a compromised downstream proteolytic machinery. Molecular fragments accumulated to a greater extent from the D90A mutant enzyme might contribute to the motor neurone degeneration. We also determined the other SOD isoenzymes: in the controls, CuZn-SOD contributed 75%, extracellular SOD 25% and Mn-SOD <5% of the total SOD activity. There was no difference in the amount of extracellular SOD between any of the groups.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Cell- och molekylärbiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Cell and Molecular Biology (hsv//eng)

Keyword

Amyotrophic lateral sclerosis
Cerebrospinal fluid
Oxygen radicals
Superoxide dismutase

Publication and Content Type

ref (subject category)
art (subject category)

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By the author/editor
Jacobsson, Johan
Jonsson, Andreas ...
Andersen, Peter ...
Forsgren, Lars
Marklund, Stefan ...
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Cell and Molecul ...
Articles in the publication
Brain
By the university
Umeå University

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