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Journal article

Mitochondrial dysfunction and increased glycolysis in prodromal and early Parkinson's blood cells

Abstract:

Background: Although primarily a neurodegenerative process, there is increasing awareness of peripheral disease mechanisms in Parkinson's disease. To investigate disease processes in accessible patient cells, we studied peripheral blood mononuclear cells in recently diagnosed PD patients and rapid eye movement‐sleep behavior disorder patients who have a greatly increased risk of developing PD. We hypothesized that peripheral blood mononuclear cells may recapitulate cellular pathology found in the PD brain and investigated these cells for mitochondrial dysfunction and oxidative stress.

Methods: Peripheral blood mononuclear cells were isolated and studied from PD patients, rapid eye movement‐sleep behavior disorder patients and age‐ and sex‐matched control individuals from the well‐characterized Oxford Discovery cohort. All participants underwent thorough clinical assessment.

Results: Initial characterization showed that PD patients had elevated levels of CD14 + monocytes and monocytes expressing C‐C motif chemokine receptor 2. Mitochondrial dysfunction and oxidative stress were increased in PD patient peripheral blood mononuclear cells, with elevated levels of mitochondrial reactive oxygen species specifically in patient monocytes. This was combined with reduced levels of the antioxidant superoxide dismutase in blood cells from PD patients and, importantly, also in rapid eye movement‐sleep behavior disorder patients. This mitochondrial dysfunction was associated with a concomitant increase in glycolysis in both PD and rapid eye movement‐sleep behavior disorder patient blood cells independent of glucose uptake or monocyte activation.

Conclusion: This work demonstrates functional bioenergetic deficits in PD and rapid eye movement‐sleep behavior disorder patient blood cells during the early stages of human disease. © 2018 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.

Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/mds.104

Authors


More by this author
Institution:
University of Oxford
Division:
Medical Sciences
Department:
Physiology Anatomy and Genetics
Role:
Author
More by this author
Institution:
University of Oxford
Division:
Medical Sciences
Department:
Physiology Anatomy and Genetics
Role:
Author


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Funding agency for:
Simon, A
Grant:
Biomedical Research Centre, Oxford
More from this funder
Funding agency for:
Simon, A
Grant:
Biomedical Research Centre, Oxford
More from this funder
Grant:
Monument Trust Discovery Award


Publisher:
John Wiley & Sons, Ltd.
Journal:
Movement Disorders More from this journal
Volume:
33
Issue:
10
Pages:
1580-1590
Publication date:
2018-10-07
Acceptance date:
2018-05-24
DOI:
EISSN:
1531-8257
ISSN:
0885-3185


Keywords:
Pubs id:
pubs:891794
UUID:
uuid:a0ef7bfa-7f30-464a-bfa7-995e40916cba
Local pid:
pubs:891794
Deposit date:
2018-07-31

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