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We are analyzing https://link.springer.com/article/10.1007/s00401-017-1746-2.

Title:
α-Synuclein transfer between neurons and astrocytes indicates that astrocytes play a role in degradation rather than in spreading | Acta Neuropathologica
Description:
Recent evidence suggests that disease progression in Parkinson’s disease (PD) could occur by the spreading of α-synuclein (α-syn) aggregates between neurons. Here we studied the role of astrocytes in the intercellular transfer and fate of α-syn fibrils, using in vitro and ex vivo models. α-Syn fibrils can be transferred to neighboring cells; however, the transfer efficiency changes depending on the cell types. We found that α-syn is efficiently transferred from astrocytes to astrocytes and from neurons to astrocytes, but less efficiently from astrocytes to neurons. Interestingly, α-syn puncta are mainly found inside the lysosomal compartments of the recipient cells. However, differently from neurons, astrocytes are able to efficiently degrade fibrillar α-syn, suggesting an active role for these cells in clearing α-syn deposits. Astrocytes co-cultured with organotypic brain slices are able to take up α-syn fibrils from the slices. Altogether our data support a role for astrocytes in trapping and clearing α-syn pathological deposits in PD.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Telecommunications

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

The income method remains a mystery to us.

Websites don't always need to be profitable; some serve as platforms for education or personal expression. Websites can serve multiple purposes. And this might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {🔍}

pubmed, article, google, scholar, cas, alphasynuclein, central, astrocytes, disease, neurons, cell, parkinsons, supplementary, material, pdf, αsyn, cells, bousset, aggregates, human, acta, αsynuclein, transfer, melki, fibrils, access, france, spreading, loria, lysosomal, transmission, neurosci, recherche, privacy, cookies, content, role, zurzolo, astrocyte, protein, plos, doijournalpone, nat, neurobiol, biol, lewy, lee, institut, fondation, data,

Topics {✒️}

month download article/chapter clearing α-syn deposits neuronal-glial cultures van der perren région ile-de-france marie skłodowska-curie fellowship extracellular alpha-synuclein species astrocyte-neuron metabolic cooperation jpnd-neutargets-anr-14-jpcd-0002-02 alpha-synuclein locus triplication neuron-specific protein localized extracellular alpha-synuclein aggregates alpha-synuclein lewy neurite alpha-synuclein amyloid aggregates vitro alpha-synuclein neurotoxicity alpha-synuclein immunoreactive astrocytes full article pdf endo-lysosomal system α-synuclein transfer di monte da ec joint programme fondation de france organotypic brain slices α-synuclein spread privacy choices/manage cookies α-syn fibrils α-syn puncta manning-bog ab alpha-synuclein spreading alpha-synuclein transfers institut de france article loria neuronal cell death rey nl robust rat model alpha-synuclein fibrils alpha-synuclein strains alpha-synuclein assembly alpha-synuclein propagates lee hj astrocyte activation fondation bettencourt-schueller human neuroblastoma cells chiara zurzolo alpha-synuclein aggregates disease suggest host lysosomal storage disorder france parkinson grant cultured human cells alpha-synuclein mice

Questions {❓}

  • α-Synuclein and Glia in Parkinson’s Disease: A Beneficial or a Detrimental Duet for the Endo-Lysosomal System?

Schema {🗺️}

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         description:Recent evidence suggests that disease progression in Parkinson’s disease (PD) could occur by the spreading of α-synuclein (α-syn) aggregates between neurons. Here we studied the role of astrocytes in the intercellular transfer and fate of α-syn fibrils, using in vitro and ex vivo models. α-Syn fibrils can be transferred to neighboring cells; however, the transfer efficiency changes depending on the cell types. We found that α-syn is efficiently transferred from astrocytes to astrocytes and from neurons to astrocytes, but less efficiently from astrocytes to neurons. Interestingly, α-syn puncta are mainly found inside the lysosomal compartments of the recipient cells. However, differently from neurons, astrocytes are able to efficiently degrade fibrillar α-syn, suggesting an active role for these cells in clearing α-syn deposits. Astrocytes co-cultured with organotypic brain slices are able to take up α-syn fibrils from the slices. Altogether our data support a role for astrocytes in trapping and clearing α-syn pathological deposits in PD.
         datePublished:2017-07-19T00:00:00Z
         dateModified:2017-07-19T00:00:00Z
         pageStart:789
         pageEnd:808
         sameAs:https://doi.org/10.1007/s00401-017-1746-2
         keywords:
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            Intercellular spreading
            Primary cultures
            Organotypic cultures
            Parkinson’s disease
            Pathology
            Neurosciences
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      headline:α-Synuclein transfer between neurons and astrocytes indicates that astrocytes play a role in degradation rather than in spreading
      description:Recent evidence suggests that disease progression in Parkinson’s disease (PD) could occur by the spreading of α-synuclein (α-syn) aggregates between neurons. Here we studied the role of astrocytes in the intercellular transfer and fate of α-syn fibrils, using in vitro and ex vivo models. α-Syn fibrils can be transferred to neighboring cells; however, the transfer efficiency changes depending on the cell types. We found that α-syn is efficiently transferred from astrocytes to astrocytes and from neurons to astrocytes, but less efficiently from astrocytes to neurons. Interestingly, α-syn puncta are mainly found inside the lysosomal compartments of the recipient cells. However, differently from neurons, astrocytes are able to efficiently degrade fibrillar α-syn, suggesting an active role for these cells in clearing α-syn deposits. Astrocytes co-cultured with organotypic brain slices are able to take up α-syn fibrils from the slices. Altogether our data support a role for astrocytes in trapping and clearing α-syn pathological deposits in PD.
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      dateModified:2017-07-19T00:00:00Z
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         α-Synuclein
         Intercellular spreading
         Primary cultures
         Organotypic cultures
         Parkinson’s disease
         Pathology
         Neurosciences
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