Your browser doesn't support javascript.
loading
CSF-1 controls cerebellar microglia and is required for motor function and social interaction.
Kana, Veronika; Desland, Fiona A; Casanova-Acebes, Maria; Ayata, Pinar; Badimon, Ana; Nabel, Elisa; Yamamuro, Kazuhiko; Sneeboer, Marjolein; Tan, I-Li; Flanigan, Meghan E; Rose, Samuel A; Chang, Christie; Leader, Andrew; Le Bourhis, Hortense; Sweet, Eric S; Tung, Navpreet; Wroblewska, Aleksandra; Lavin, Yonit; See, Peter; Baccarini, Alessia; Ginhoux, Florent; Chitu, Violeta; Stanley, E Richard; Russo, Scott J; Yue, Zhenyu; Brown, Brian D; Joyner, Alexandra L; De Witte, Lotje D; Morishita, Hirofumi; Schaefer, Anne; Merad, Miriam.
Afiliação
  • Kana V; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Desland FA; Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Casanova-Acebes M; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Ayata P; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Badimon A; Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Nabel E; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Yamamuro K; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Sneeboer M; Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Tan IL; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Flanigan ME; Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Rose SA; Ronald M. Loeb Center for Alzheimer's Disease, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Chang C; Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Leader A; Ronald M. Loeb Center for Alzheimer's Disease, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Le Bourhis H; Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Sweet ES; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Tung N; Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Wroblewska A; Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Lavin Y; Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • See P; Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Baccarini A; Department of Ophthalmology, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Ginhoux F; Mindich Child Health and Development Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Chitu V; Department of Psychiatry, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Stanley ER; Department of Translational Neuroscience, Brain Center Rudolf Magnus, University Medical Center Utrecht, Utrecht University, Utrecht, Netherlands.
  • Russo SJ; Developmental Biology Program, Memorial Sloan-Kettering Cancer Center, New York, NY.
  • Yue Z; Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Brown BD; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Joyner AL; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
  • De Witte LD; Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Morishita H; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Schaefer A; Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY.
  • Merad M; Precision Immunology Institute, Icahn School of Medicine at Mount Sinai, New York, NY.
J Exp Med ; 216(10): 2265-2281, 2019 10 07.
Article em En | MEDLINE | ID: mdl-31350310
ABSTRACT
Microglia, the brain resident macrophages, critically shape forebrain neuronal circuits. However, their precise function in the cerebellum is unknown. Here we show that human and mouse cerebellar microglia express a unique molecular program distinct from forebrain microglia. Cerebellar microglial identity was driven by the CSF-1R ligand CSF-1, independently of the alternate CSF-1R ligand, IL-34. Accordingly, CSF-1 depletion from Nestin+ cells led to severe depletion and transcriptional alterations of cerebellar microglia, while microglia in the forebrain remained intact. Strikingly, CSF-1 deficiency and alteration of cerebellar microglia were associated with reduced Purkinje cells, altered neuronal function, and defects in motor learning and social novelty interactions. These findings reveal a novel CSF-1-CSF-1R signaling-mediated mechanism that contributes to motor function and social behavior.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células de Purkinje / Comportamento Social / Comportamento Animal / Transdução de Sinais / Fator Estimulador de Colônias de Macrófagos / Microglia / Atividade Motora Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Células de Purkinje / Comportamento Social / Comportamento Animal / Transdução de Sinais / Fator Estimulador de Colônias de Macrófagos / Microglia / Atividade Motora Idioma: En Ano de publicação: 2019 Tipo de documento: Article