Your browser doesn't support javascript.
loading
Astrocytes mediate synapse elimination through MEGF10 and MERTK pathways.
Chung, Won-Suk; Clarke, Laura E; Wang, Gordon X; Stafford, Benjamin K; Sher, Alexander; Chakraborty, Chandrani; Joung, Julia; Foo, Lynette C; Thompson, Andrew; Chen, Chinfei; Smith, Stephen J; Barres, Ben A.
Afiliação
  • Chung WS; Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
  • Clarke LE; Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
  • Wang GX; Department of Molecular and Cellular Physiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
  • Stafford BK; Department of Ophthalmology and Visual Sciences, University of Michigan, Ann Arbor, MI 48105, USA.
  • Sher A; Santa Cruz Institute of Particle Physic and Department of Physics, University of California, Santa Cruz, CA 95064.
  • Chakraborty C; Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
  • Joung J; Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
  • Foo LC; Institute of Molecular and Cell Biology, AStar, 61 Biopolis Drive, Proteos Building, Singapore 138673.
  • Thompson A; Children's Hospital, Harvard Medical School, 300 Longwood Ave., CLS12250, Boston, MA 02115.
  • Chen C; Children's Hospital, Harvard Medical School, 300 Longwood Ave., CLS12250, Boston, MA 02115.
  • Smith SJ; Department of Molecular and Cellular Physiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
  • Barres BA; Department of Neurobiology, Stanford University, School of Medicine, Stanford, CA 94305, USA.
Nature ; 504(7480): 394-400, 2013 Dec 19.
Article em En | MEDLINE | ID: mdl-24270812
To achieve its precise neural connectivity, the developing mammalian nervous system undergoes extensive activity-dependent synapse remodelling. Recently, microglial cells have been shown to be responsible for a portion of synaptic pruning, but the remaining mechanisms remain unknown. Here we report a new role for astrocytes in actively engulfing central nervous system synapses. This process helps to mediate synapse elimination, requires the MEGF10 and MERTK phagocytic pathways, and is strongly dependent on neuronal activity. Developing mice deficient in both astrocyte pathways fail to refine their retinogeniculate connections normally and retain excess functional synapses. Finally, we show that in the adult mouse brain, astrocytes continuously engulf both excitatory and inhibitory synapses. These studies reveal a novel role for astrocytes in mediating synapse elimination in the developing and adult brain, identify MEGF10 and MERTK as critical proteins in the synapse remodelling underlying neural circuit refinement, and have important implications for understanding learning and memory as well as neurological disease processes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fagocitose / Sinapses / Astrócitos / Proteínas Proto-Oncogênicas / Receptores Proteína Tirosina Quinases / Proteínas de Membrana / Vias Neurais Idioma: En Ano de publicação: 2013 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fagocitose / Sinapses / Astrócitos / Proteínas Proto-Oncogênicas / Receptores Proteína Tirosina Quinases / Proteínas de Membrana / Vias Neurais Idioma: En Ano de publicação: 2013 Tipo de documento: Article