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Microglia response following acute demyelination is heterogeneous and limits infiltrating macrophage dispersion.
Plemel, Jason R; Stratton, Jo Anne; Michaels, Nathan J; Rawji, Khalil S; Zhang, Eric; Sinha, Sarthak; Baaklini, Charbel S; Dong, Yifei; Ho, Madelene; Thorburn, Kevin; Friedman, Timothy N; Jawad, Sana; Silva, Claudia; Caprariello, Andrew V; Hoghooghi, Vahid; Yue, Julie; Jaffer, Arzina; Lee, Kelly; Kerr, Bradley J; Midha, Raj; Stys, Peter K; Biernaskie, Jeff; Yong, V Wee.
Afiliação
  • Plemel JR; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Stratton JA; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Michaels NJ; Department of Medicine, Division of Neurology, University of Alberta, Edmonton, Alberta, Canada.
  • Rawji KS; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Zhang E; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Sinha S; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Baaklini CS; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Dong Y; Department of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Ho M; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Thorburn K; Department of Medicine, Division of Neurology, University of Alberta, Edmonton, Alberta, Canada.
  • Friedman TN; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Jawad S; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Silva C; Department of Pharmacology, University of Alberta, Edmonton, Alberta, Canada.
  • Caprariello AV; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Hoghooghi V; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Yue J; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Jaffer A; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Lee K; Hotchkiss Brain Institute and Department of Clinical Neurosciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Kerr BJ; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Midha R; Department of Comparative Biology and Experimental Medicine, Faculty of Veterinary Medicine, University of Calgary, Calgary, Alberta, Canada.
  • Stys PK; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Biernaskie J; Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Alberta, Canada.
  • Yong VW; Department of Anesthesiology and Pain Medicine, University of Alberta, Edmonton, Alberta, Canada.
Sci Adv ; 6(3): eaay6324, 2020 01.
Article em En | MEDLINE | ID: mdl-31998844
ABSTRACT
Microglia and infiltrating macrophages are thought to orchestrate the central nervous system (CNS) response to injury; however, the similarities between these cells make it challenging to distinguish their relative contributions. We genetically labeled microglia and CNS-associated macrophages to distinguish them from infiltrating macrophages. Using single-cell RNA sequencing, we describe multiple microglia activation states, one of which was enriched for interferon associated signaling. Although blood-derived macrophages acutely infiltrated the demyelinated lesion, microglia progressively monopolized the lesion environment where they surrounded infiltrating macrophages. In the microglia-devoid sciatic nerve, the infiltrating macrophage response was sustained. In the CNS, the preferential proliferation of microglia and sparse microglia death contributed to microglia dominating the lesion. Microglia ablation reversed the spatial restriction of macrophages with the demyelinated spinal cord, highlighting an unrealized macrophages-microglia interaction. The restriction of peripheral inflammation by microglia may be a previously unidentified mechanism by which the CNS maintains its "immune privileged" status.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Desmielinizantes / Microglia / Macrófagos Idioma: En Revista: Sci Adv Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Desmielinizantes / Microglia / Macrófagos Idioma: En Revista: Sci Adv Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá