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Underpinning heterogeneity in synaptic transmission by presynaptic ensembles of distinct morphological modules.
Fekete, Adam; Nakamura, Yukihiro; Yang, Yi-Mei; Herlitze, Stefan; Mark, Melanie D; DiGregorio, David A; Wang, Lu-Yang.
Afiliação
  • Fekete A; Program in Neurosciences and Mental Health, The Hospital for Sick Children, 555 University Ave, Toronto, ON, M5G 1X8, Canada.
  • Nakamura Y; Department of Physiology, University of Toronto, Toronto, ON, M5S 1A8, Canada.
  • Yang YM; Department of Pharmacology, Jikei University School of Medicine, Nishishinbashi, Minato-ku, Tokyo, 1058461, Japan.
  • Herlitze S; Program in Neurosciences and Mental Health, The Hospital for Sick Children, 555 University Ave, Toronto, ON, M5G 1X8, Canada.
  • Mark MD; Department of Physiology, University of Toronto, Toronto, ON, M5S 1A8, Canada.
  • DiGregorio DA; Department of Biomedical Sciences, University of Minnesota Medical School, 1035 University Drive, Duluth, MN, 55812, USA.
  • Wang LY; Department of General Zoology and Neurobiology, Ruhr-University Bochum, Universitätsstrasse 150, D-44780, Bochum, Germany.
Nat Commun ; 10(1): 826, 2019 02 18.
Article em En | MEDLINE | ID: mdl-30778063
ABSTRACT
Synaptic heterogeneity is widely observed but its underpinnings remain elusive. We addressed this issue using mature calyx of Held synapses whose numbers of bouton-like swellings on stalks of the nerve terminals inversely correlate with release probability (Pr). We examined presynaptic Ca2+ currents and transients, topology of fluorescently tagged knock-in Ca2+ channels, and Ca2+ channel-synaptic vesicle (SV) coupling distance using Ca2+ chelator and inhibitor of septin cytomatrix in morphologically diverse synapses. We found that larger clusters of Ca2+ channels with tighter coupling distance to SVs elevate Pr in stalks, while smaller clusters with looser coupling distance lower Pr in swellings. Septin is a molecular determinant of the differences in coupling distance. Supported by numerical simulations, we propose that varying the ensemble of two morphological modules containing distinct Ca2+ channel-SV topographies diversifies Pr in the terminal, thereby establishing a morpho-functional continuum that expands the coding capacity within a single synapse population.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Commun Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Nat Commun Ano de publicação: 2019 Tipo de documento: Article