Literature DB >> 15182716

Modulation of glutamate mobility reveals the mechanism underlying slow-rising AMPAR EPSCs and the diffusion coefficient in the synaptic cleft.

Thomas A Nielsen1, David A DiGregorio, R Angus Silver.   

Abstract

Fast- and slow-rising AMPA receptor-mediated EPSCs occur at central synapses. Fast-rising EPSCs are thought to be mediated by rapid local release of glutamate. However, two controversial mechanisms have been proposed to underlie slow-rising EPSCs: prolonged local release of transmitter via a fusion pore, and spillover of transmitter released rapidly from distant sites. We have investigated the mechanism underlying slow-rising EPSCs and the diffusion coefficient of glutamate in the synaptic cleft (Dglut) at cerebellar mossy fiber-granule cell synapses using a combination of diffusion modeling and patch-clamp recording. Simulations show that modulating Dglut has different effects on the peak amplitudes and time courses of EPSCs mediated by these two mechanisms. Slowing diffusion with the macromolecule dextran slowed slow-rising EPSCs and had little effect on their amplitude, indicating that glutamate spillover underlies these currents. Our results also suggest that under control conditions Dglut is approximately 3-fold lower than in free solution.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 15182716     DOI: 10.1016/j.neuron.2004.04.003

Source DB:  PubMed          Journal:  Neuron        ISSN: 0896-6273            Impact factor:   17.173


  99 in total

1.  Hydrodynamic flow in a synaptic cleft during exocytosis.

Authors:  M N Shneider; R S Gimatdinov; A I Skorinkin; I V Kovyazina; E E Nikolsky
Journal:  Eur Biophys J       Date:  2011-11-01       Impact factor: 1.733

2.  Mechanisms underlying signal filtering at a multisynapse contact.

Authors:  Timotheus Budisantoso; Ko Matsui; Naomi Kamasawa; Yugo Fukazawa; Ryuichi Shigemoto
Journal:  J Neurosci       Date:  2012-02-15       Impact factor: 6.167

3.  Measuring action potential-evoked transmission at individual synaptic contacts.

Authors:  David W Nauen; Guo-Qiang Bi
Journal:  J Neural Eng       Date:  2012-06       Impact factor: 5.379

4.  Channel-opening kinetic mechanism for human wild-type GluK2 and the M867I mutant kainate receptor.

Authors:  Yan Han; Congzhou Wang; Jae Seon Park; Li Niu
Journal:  Biochemistry       Date:  2010-11-02       Impact factor: 3.162

5.  GABAA receptor kinetics in the cerebellar nuclei: evidence for detection of transmitter from distant release sites.

Authors:  Jason R Pugh; Indira M Raman
Journal:  Biophys J       Date:  2004-12-30       Impact factor: 4.033

6.  Deriving the glutamate clearance time course from transporter currents in CA1 hippocampal astrocytes: transmitter uptake gets faster during development.

Authors:  Jeffrey S Diamond
Journal:  J Neurosci       Date:  2005-03-16       Impact factor: 6.167

7.  Differential control of synaptic and ectopic vesicular release of glutamate.

Authors:  Ko Matsui; Craig E Jahr
Journal:  J Neurosci       Date:  2004-10-13       Impact factor: 6.167

8.  Release kinetics, quantal parameters and their modulation during short-term depression at a developing synapse in the rat CNS.

Authors:  Holger Taschenberger; Volker Scheuss; Erwin Neher
Journal:  J Physiol       Date:  2005-08-11       Impact factor: 5.182

9.  Dynamics of fast and slow inhibition from cerebellar golgi cells allow flexible control of synaptic integration.

Authors:  John J Crowley; Diasynou Fioravante; Wade G Regehr
Journal:  Neuron       Date:  2009-09-24       Impact factor: 17.173

10.  Input-specific GABAergic signaling to newborn neurons in adult dentate gyrus.

Authors:  Sean J Markwardt; Jacques I Wadiche; Linda S Overstreet-Wadiche
Journal:  J Neurosci       Date:  2009-12-02       Impact factor: 6.167

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.