Your browser doesn't support javascript.
loading
Chemico-genetic discovery of astrocytic control of inhibition in vivo.
Takano, Tetsuya; Wallace, John T; Baldwin, Katherine T; Purkey, Alicia M; Uezu, Akiyoshi; Courtland, Jamie L; Soderblom, Erik J; Shimogori, Tomomi; Maness, Patricia F; Eroglu, Cagla; Soderling, Scott H.
Afiliação
  • Takano T; The Department of Cell Biology, Duke University Medical School, Durham, NC, USA. tetsuya.takano@keio.jp.
  • Wallace JT; The Department of Cell Biology, Duke University Medical School, Durham, NC, USA.
  • Baldwin KT; The Department of Cell Biology, Duke University Medical School, Durham, NC, USA.
  • Purkey AM; The Department of Cell Biology, Duke University Medical School, Durham, NC, USA.
  • Uezu A; The Department of Cell Biology, Duke University Medical School, Durham, NC, USA.
  • Courtland JL; Department of Neurobiology, Duke University Medical School, Durham, NC, USA.
  • Soderblom EJ; The Department of Cell Biology, Duke University Medical School, Durham, NC, USA.
  • Shimogori T; Duke Proteomics and Metabolomics Shared Resource and Duke Center for Genomic and Computational Biology, Duke University Medical School, Durham, NC, USA.
  • Maness PF; Molecular Mechanisms of Brain Development, Center for Brain Science (CBS), RIKEN, Saitama, Japan.
  • Eroglu C; Department of Biochemistry, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
  • Soderling SH; Department of Biophysics, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Nature ; 588(7837): 296-302, 2020 12.
Article em En | MEDLINE | ID: mdl-33177716
Perisynaptic astrocytic processes are an integral part of central nervous system synapses1,2; however, the molecular mechanisms that govern astrocyte-synapse adhesions and how astrocyte contacts control synapse formation and function are largely unknown. Here we use an in vivo chemico-genetic approach that applies a cell-surface fragment complementation strategy, Split-TurboID, and identify a proteome that is enriched at astrocyte-neuron junctions in vivo, which includes neuronal cell adhesion molecule (NRCAM). We find that NRCAM is expressed in cortical astrocytes, localizes to perisynaptic contacts and is required to restrict neuropil infiltration by astrocytic processes. Furthermore, we show that astrocytic NRCAM interacts transcellularly with neuronal NRCAM coupled to gephyrin at inhibitory postsynapses. Depletion of astrocytic NRCAM reduces numbers of inhibitory synapses without altering glutamatergic synaptic density. Moreover, loss of astrocytic NRCAM markedly decreases inhibitory synaptic function, with minor effects on excitation. Thus, our results present a proteomic framework for how astrocytes interface with neurons and reveal how astrocytes control GABAergic synapse formation and function.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinapses / Astrócitos / Proteoma / Proteômica / Neurônios Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sinapses / Astrócitos / Proteoma / Proteômica / Neurônios Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article