Microglia deficiency accelerates prion disease but does not enhance prion accumulation in the brain
© 2022 The Authors. GLIA published by Wiley Periodicals LLC..
Prion diseases are transmissible, neurodegenerative disorders associated with misfolding of the prion protein. Previous studies show that reduction of microglia accelerates central nervous system (CNS) prion disease and increases the accumulation of prions in the brain, suggesting that microglia provide neuroprotection by phagocytosing and destroying prions. In Csf1rΔFIRE mice, the deletion of an enhancer within Csf1r specifically blocks microglia development, however, their brains develop normally and show none of the deficits reported in other microglia-deficient models. Csf1rΔFIRE mice were used as a refined model in which to study the impact of microglia-deficiency on CNS prion disease. Although Csf1rΔFIRE mice succumbed to CNS prion disease much earlier than wild-type mice, the accumulation of prions in their brains was reduced. Instead, astrocytes displayed earlier, non-polarized reactive activation with enhanced phagocytosis of neuronal contents and unfolded protein responses. Our data suggest that rather than simply phagocytosing and destroying prions, the microglia instead provide host-protection during CNS prion disease and restrict the harmful activities of reactive astrocytes.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2022 |
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| Erschienen: |
2022 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:70 |
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| Enthalten in: |
Glia - 70(2022), 11 vom: 19. Nov., Seite 2169-2187 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Bradford, Barry M [VerfasserIn] |
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| Links: |
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| Themen: |
Central nervous system |
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| Anmerkungen: |
Date Completed 14.09.2022 Date Revised 22.03.2023 published: Print-Electronic Citation Status MEDLINE |
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| doi: |
10.1002/glia.24244 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM343721856 |
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| 245 | 1 | 0 | |a Microglia deficiency accelerates prion disease but does not enhance prion accumulation in the brain |
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| 520 | |a © 2022 The Authors. GLIA published by Wiley Periodicals LLC. | ||
| 520 | |a Prion diseases are transmissible, neurodegenerative disorders associated with misfolding of the prion protein. Previous studies show that reduction of microglia accelerates central nervous system (CNS) prion disease and increases the accumulation of prions in the brain, suggesting that microglia provide neuroprotection by phagocytosing and destroying prions. In Csf1rΔFIRE mice, the deletion of an enhancer within Csf1r specifically blocks microglia development, however, their brains develop normally and show none of the deficits reported in other microglia-deficient models. Csf1rΔFIRE mice were used as a refined model in which to study the impact of microglia-deficiency on CNS prion disease. Although Csf1rΔFIRE mice succumbed to CNS prion disease much earlier than wild-type mice, the accumulation of prions in their brains was reduced. Instead, astrocytes displayed earlier, non-polarized reactive activation with enhanced phagocytosis of neuronal contents and unfolded protein responses. Our data suggest that rather than simply phagocytosing and destroying prions, the microglia instead provide host-protection during CNS prion disease and restrict the harmful activities of reactive astrocytes | ||
| 650 | 4 | |a Journal Article | |
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| 650 | 4 | |a central nervous system | |
| 650 | 4 | |a microglia | |
| 650 | 4 | |a neurodegeneration | |
| 650 | 4 | |a prion disease | |
| 650 | 4 | |a reactive astrocyte | |
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| 700 | 1 | |a McGuire, Lynne I |e verfasserin |4 aut | |
| 700 | 1 | |a Hume, David A |e verfasserin |4 aut | |
| 700 | 1 | |a Pridans, Clare |e verfasserin |4 aut | |
| 700 | 1 | |a Mabbott, Neil A |e verfasserin |4 aut | |
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