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Exposure of alpha-Synuclein Aggregates to Organotypic Slice Cultures Recapitulates Key Molecular Features of Parkinsons Disease

Moudio, Serge (author)
Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten,Region Östergötland, Klinisk patologi
Rodin, Fredrik (author)
Linköpings universitet,Medicinska fakulteten,Avdelningen för neurobiologi,Region Östergötland, Klinisk patologi
Albargothy, Nazira (author)
Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten,Region Östergötland, Klinisk patologi
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Karlsson, Urban (author)
Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten
Reyes, Juan (author)
Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten,Region Östergötland, Klinisk patologi
Hallbeck, Martin (author)
Linköpings universitet,Avdelningen för neurobiologi,Medicinska fakulteten,Region Östergötland, Klinisk patologi
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 (creator_code:org_t)
2022-02-16
2022
English.
In: Frontiers in Neurology. - : Frontiers Media SA. - 1664-2295. ; 13
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The accumulation of proteinaceous deposits comprised largely of the alpha-synuclein protein is one of the main hallmarks of Parkinsons disease (PD) and related synucleinopathies. Their progressive development coincides with site-specific phosphorylation, oxidative stress and eventually, compromised neuronal function. However, modeling protein aggregate formation in animal or in vitro models has proven notably difficult. Here, we took advantage of a preclinical organotypic brain slice culture model to study alpha-synuclein aggregate formation ex vivo. We monitored the progressive and gradual changes induced by alpha-synuclein such as cellular toxicity, autophagy activation, mitochondrial dysfunction, cellular death as well as alpha-synuclein modification including site-specific phosphorylation. Our results demonstrate that organotypic brain slice cultures can be cultured for long periods of time and when cultured in the presence of aggregated alpha-synuclein, the molecular features of PD are recapitulated. Taken together, this ex vivo model allows for detailed modeling of the molecular features of PD, thus enabling studies on the cumulative effects of alpha-synuclein in a complex environment. This provides a platform to screen potential disease-modifying therapeutic candidates aimed at impeding alpha-synuclein aggregation and/or cellular transmission. Moreover, this model provides a robust replacement for in vivo studies that do not include behavioral experiments, thus providing a way to reduce the number of animals used in an accelerated timescale.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

Parkinsons disease; alpha-synuclein; PFF; organotypic slice cultures; autophagy; 3R; Lewy bodies; model of CNS disease

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By the author/editor
Moudio, Serge
Rodin, Fredrik
Albargothy, Nazi ...
Karlsson, Urban
Reyes, Juan
Hallbeck, Martin
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Neurosciences
Articles in the publication
Frontiers in Neu ...
By the university
Linköping University

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