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New tools for studying microglia in the mouse and human CNS.
Bennett, Mariko L; Bennett, F Chris; Liddelow, Shane A; Ajami, Bahareh; Zamanian, Jennifer L; Fernhoff, Nathaniel B; Mulinyawe, Sara B; Bohlen, Christopher J; Adil, Aykezar; Tucker, Andrew; Weissman, Irving L; Chang, Edward F; Li, Gordon; Grant, Gerald A; Hayden Gephart, Melanie G; Barres, Ben A.
Afiliação
  • Bennett ML; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; marikobennett@stanford.edu barres@stanford.edu.
  • Bennett FC; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305;
  • Liddelow SA; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; Department of Pharmacology and Therapeutics, University of Melbourne, Melbourne, VIC, Australia, 3010;
  • Ajami B; Department of Neurology, Stanford University School of Medicine, Stanford, CA 94305;
  • Zamanian JL; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305;
  • Fernhoff NB; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305; Ludwig Center for Cancer Stem Cell Research and Medicine, Stanford University School of Medicine, Stanford, CA 94305; Stanford Cancer Institute, Stanford University School of Medici
  • Mulinyawe SB; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305;
  • Bohlen CJ; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305;
  • Adil A; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305;
  • Tucker A; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305;
  • Weissman IL; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305; Ludwig Center for Cancer Stem Cell Research and Medicine, Stanford University School of Medicine, Stanford, CA 94305; Stanford Cancer Institute, Stanford University School of Medici
  • Chang EF; University of California, San Francisco Epilepsy Center, University of California, San Francisco, CA 94143;
  • Li G; Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305.
  • Grant GA; Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305.
  • Hayden Gephart MG; Department of Neurosurgery, Stanford University School of Medicine, Stanford, CA 94305.
  • Barres BA; Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305; marikobennett@stanford.edu barres@stanford.edu.
Proc Natl Acad Sci U S A ; 113(12): E1738-46, 2016 Mar 22.
Article em En | MEDLINE | ID: mdl-26884166
ABSTRACT
The specific function of microglia, the tissue resident macrophages of the brain and spinal cord, has been difficult to ascertain because of a lack of tools to distinguish microglia from other immune cells, thereby limiting specific immunostaining, purification, and manipulation. Because of their unique developmental origins and predicted functions, the distinction of microglia from other myeloid cells is critically important for understanding brain development and disease; better tools would greatly facilitate studies of microglia function in the developing, adult, and injured CNS. Here, we identify transmembrane protein 119 (Tmem119), a cell-surface protein of unknown function, as a highly expressed microglia-specific marker in both mouse and human. We developed monoclonal antibodies to its intracellular and extracellular domains that enable the immunostaining of microglia in histological sections in healthy and diseased brains, as well as isolation of pure nonactivated microglia by FACS. Using our antibodies, we provide, to our knowledge, the first RNAseq profiles of highly pure mouse microglia during development and after an immune challenge. We used these to demonstrate that mouse microglia mature by the second postnatal week and to predict novel microglial functions. Together, we anticipate these resources will be valuable for the future study and understanding of microglia in health and disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Microglia / Proteínas de Membrana / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Microglia / Proteínas de Membrana / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2016 Tipo de documento: Article
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