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  Phagocyte-mediated synapse removal in cortical neuroinflammation is promoted by local calcium accumulation

Jafari, M., Schumacher, A.-M., Snaidero, N., Ullrich Gavilanes, E. M., Neziraj, T., Kocsis-Jutka, V., et al. (2021). Phagocyte-mediated synapse removal in cortical neuroinflammation is promoted by local calcium accumulation. Nature Neuroscience, 24, 355-367. doi:10.1038/s41593-020-00780-7.

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Jafari, Mehrnoosh, Author
Schumacher, Adrian-Minh, Author
Snaidero, Nicolas, Author
Ullrich Gavilanes, Emily M., Author
Neziraj, Tradite, Author
Kocsis-Jutka, Virág, Author
Engels, Daniel, Author
Jürgens, Tanja, Author
Wagner, Ingrid, Author
Flórez-Weidinger, Juan Daniel1, Author           
Schmidt, Stephanie S., Author
Beltrán, Eduardo, Author
Hagan, Nellwyn, Author
Woodworth, Lisa, Author
Ofengeim, Dimitry, Author
Gans, Joseph, Author
Wolf, Fred1, Author           
Kreutzfeldt, Mario, Author
Portugues, Ruben, Author
Merkler, Doron, Author
Misgeld, Thomas, AuthorKerschensteiner, Martin, Author more..
Affiliations:
1Research Group Theoretical Neurophysics, Max Planck Institute for Dynamics and Self-Organization, Max Planck Society, ou_2063289              

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 Abstract: Cortical pathology contributes to chronic cognitive impairment of patients suffering from the neuroinflammatory disease multiple sclerosis (MS). How such gray matter inflammation affects neuronal structure and function is not well understood. In
the present study, we use functional and structural in vivo imaging in a mouse model of cortical MS to demonstrate that bouts
of cortical inflammation disrupt cortical circuit activity coincident with a widespread, but transient, loss of dendritic spines.
Spines destined for removal show local calcium accumulations and are subsequently removed by invading macrophages or
activated microglia. Targeting phagocyte activation with a new antagonist of the colony-stimulating factor 1 receptor prevents
cortical synapse loss. Overall, our study identifies synapse loss as a key pathological feature of inflammatory gray matter
lesions that is amenable to immunomodulatory therapy.

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 Dates: 2021-01-252021
 Publication Status: Issued
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 Publishing info: -
 Table of Contents: -
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 Identifiers: DOI: 10.1038/s41593-020-00780-7
 Degree: -

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Title: Nature Neuroscience
Source Genre: Journal
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Pages: - Volume / Issue: 24 Sequence Number: - Start / End Page: 355 - 367 Identifier: ISSN: 1097-6256
ISSN: 1546-1726