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PARKIN is not required to sustain OXPHOS function in adult mammalian tissues

Filograna, Roberta (author)
Karolinska Institute,Karolinska Institutet
Gerlach, Jule (author)
Karolinska Institute
Choi, Hae-Na (author)
University of Cologne
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Rigoni, Giovanni (author)
Karolinska Institute
Barbaro, Michela (author)
Karolinska University Hospital
Oscarson, Mikael (author)
Karolinska University Hospital
Lee, Seungmin (author)
Karolinska Institute
Tiklova, Katarina (author)
Karolinska Institute
Ringnér, Markus (author)
Lund University,Lunds universitet,Molekylär biovetenskap,Avdelningar vid Biologiska institutionen,Biologiska institutionen,Naturvetenskapliga fakulteten,Molecular biosciences,Sections at the Department of Biology,Department of Biology,Faculty of Science
Koolmeister, Camilla (author)
Karolinska Institute,Karolinska Institutet
Wibom, Rolf (author)
Karolinska Institutet
Riggare, Sara, PhD, 1971- (author)
Uppsala University,Uppsala universitet,E-hälsa och hälsodata
Nennesmo, Inger (author)
Karolinska Institute,Karolinska Institutet
Perlmann, Thomas (author)
Karolinska Institute
Wredenberg, Anna (author)
Karolinska Institute,Karolinska Institutet
Wedell, Anna (author)
Karolinska Institutet,Karolinska University Hospital
Motori, Elisa (author)
University of Cologne
Svenningsson, Per (author)
Karolinska Institute,Karolinska Institutet,Karolinska University Hospital
Larsson, Nils-Göran (author)
Karolinska Institute
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 (creator_code:org_t)
Springer Nature, 2024
2024
English.
In: npj Parkinson's Disease. - : Springer Nature. - 2373-8057. ; 10:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Loss-of-function variants in the PRKN gene encoding the ubiquitin E3 ligase PARKIN cause autosomal recessive early-onset Parkinson’s disease (PD). Extensive in vitro and in vivo studies have reported that PARKIN is involved in multiple pathways of mitochondrial quality control, including mitochondrial degradation and biogenesis. However, these findings are surrounded by substantial controversy due to conflicting experimental data. In addition, the existing PARKIN-deficient mouse models have failed to faithfully recapitulate PD phenotypes. Therefore, we have investigated the mitochondrial role of PARKIN during ageing and in response to stress by employing a series of conditional Parkin knockout mice. We report that PARKIN loss does not affect oxidative phosphorylation (OXPHOS) capacity and mitochondrial DNA (mtDNA) levels in the brain, heart, and skeletal muscle of aged mice. We also demonstrate that PARKIN deficiency does not exacerbate the brain defects and the pro-inflammatory phenotype observed in mice carrying high levels of mtDNA mutations. To rule out compensatory mechanisms activated during embryonic development of Parkin-deficient mice, we generated a mouse model where loss of PARKIN was induced in adult dopaminergic (DA) neurons. Surprisingly, also these mice did not show motor impairment or neurodegeneration, and no major transcriptional changes were found in isolated midbrain DA neurons. Finally, we report a patient with compound heterozygous PRKN pathogenic variants that lacks PARKIN and has developed PD. The PARKIN deficiency did not impair OXPHOS activities or induce mitochondrial pathology in skeletal muscle from the patient. Altogether, our results argue that PARKIN is dispensable for OXPHOS function in adult mammalian tissues.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)
NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)

Keyword

Medicinsk vetenskap
Medical Science

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