Literature DB >> 11600626

Characterization of the spontaneous synaptic activity of amacrine cells in the mouse retina.

M J Frech1, J Pérez-León, H Wässle, K H Backus.   

Abstract

Amacrine cells are a heterogeneous class of interneurons that modulate the transfer of the light signals through the retina. In addition to ionotropic glutamate receptors, amacrine cells express two types of inhibitory receptors, GABA(A) receptors (GABA(A)Rs) and glycine receptors (GlyRs). To characterize the functional contribution of these different receptors, spontaneous postsynaptic currents (sPSCs) were recorded with the whole cell configuration of the patch-clamp technique in acutely isolated slices of the adult mouse retina. All amacrine cells investigated (n = 47) showed spontaneous synaptic activity. In six amacrine cells, spontaneous excitatory postsynaptic currents could be identified by their sensitivity to kynurenic acid. They were characterized by small amplitudes [mean: -13.7 +/- 1.5 (SE) pA] and rapid decay kinetics (mean tau: 1.35 +/- 0.16 ms). In contrast, the reversal potential of sPSCs characterized by slow decay kinetics (amplitude-weighted time constant, tau(w), >4 ms) was dependent on the intracellular Cl(-) concentration (n = 7), indicating that they were spontaneous inhibitory postsynaptic currents (sIPSCs). In 14 of 34 amacrine cells sIPSCs were blocked by bicuculline (10 microM), indicating that they were mediated by GABA(A)Rs. Only four amacrine cells showed glycinergic sIPSCs that were inhibited by strychnine (1 microM). In one amacrine cell, sIPSCs mediated by GABA(A)Rs and GlyRs were found simultaneously. GABAergic sIPSCs could be subdivided into one group best fit by a monoexponential decay function and another biexponentially decaying group. The mean amplitude of GABAergic sIPSCs (-42.1 +/- 5.8 pA) was not significantly different from that of glycinergic sIPSCs (-28.0 +/- 8.5 pA). However, GlyRs (mean T10/90: 2.4 +/- 0.08 ms) activated significantly slower than GABA(A)Rs (mean T10/90: 1.2 +/- 0.03 ms). In addition, the decay kinetics of monoexponentially decaying GABA(A)Rs (mean tau(w): 20.3 +/- 0.50), biexponentially decaying GABA(A)Rs (mean tau(w): 30.7 +/- 0.95), and GlyRs (mean tau(w) = 25.3 +/- 1.94) were significantly different. These differences in the activation and decay kinetics of sIPSCs indicate that amacrine cells of the mouse retina express at least three types of functionally different inhibitory receptors: GlyRs and possibly two subtypes of GABA(A)Rs.

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Year:  2001        PMID: 11600626     DOI: 10.1152/jn.2001.86.4.1632

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  7 in total

1.  Functional properties of spontaneous EPSCs and non-NMDA receptors in rod amacrine (AII) cells in the rat retina.

Authors:  Margaret Lin Veruki; Svein Harald Mørkve; Espen Hartveit
Journal:  J Physiol       Date:  2003-04-17       Impact factor: 5.182

2.  Functional properties of spontaneous IPSCs and glycine receptors in rod amacrine (AII) cells in the rat retina.

Authors:  Silje Bakken Gill; Margaret Lin Veruki; Espen Hartveit
Journal:  J Physiol       Date:  2006-07-06       Impact factor: 5.182

3.  Spontaneous IPSCs and glycine receptors with slow kinetics in wide-field amacrine cells in the mature rat retina.

Authors:  Margaret Lin Veruki; Silje Bakken Gill; Espen Hartveit
Journal:  J Physiol       Date:  2007-03-01       Impact factor: 5.182

4.  Glycinergic input of widefield, displaced amacrine cells of the mouse retina.

Authors:  Sriparna Majumdar; Jan Weiss; Heinz Wässle
Journal:  J Physiol       Date:  2009-06-15       Impact factor: 5.182

Review 5.  Receptor targets of amacrine cells.

Authors:  Chi Zhang; Maureen A McCall
Journal:  Vis Neurosci       Date:  2012-01       Impact factor: 3.241

6.  A novel machine learning-based approach for the detection and analysis of spontaneous synaptic currents.

Authors:  Thomas Pircher; Bianca Pircher; Andreas Feigenspan
Journal:  PLoS One       Date:  2022-09-19       Impact factor: 3.752

7.  Niemann-Pick type C1 patient-specific induced pluripotent stem cells display disease specific hallmarks.

Authors:  Michaela Trilck; Rayk Hübner; Philip Seibler; Christine Klein; Arndt Rolfs; Moritz J Frech
Journal:  Orphanet J Rare Dis       Date:  2013-09-18       Impact factor: 4.123

  7 in total

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