Relative contributions of rod and cone bipolar cell inputs to AII amacrine cell light responses in the mouse retina.

Journal Article (Journal Article)

AII amacrine cells (AIIACs) are crucial relay stations for rod-mediated signals in the mammalian retina and they receive synaptic inputs from depolarizing and hyperpolarizing bipolar cells (DBCs and HBCs) as well as from other amacrine cells. Using whole-cell voltage-clamp technique in conjunction with pharmacological tools, we found that the light-evoked current response of AIIACs in the mouse retina is almost completely mediated by two DBC synaptic inputs: a 6,7-dinitro-quinoxaline-2,3-dione (DNQX)-resistant component mediated by cone DBCs (DBC(C)s) through an electrical synapse, and a DNQX-sensitive component mediated by rod DBCs (DBC(R)s). This scheme is supported by AIIAC current responses recorded from two knockout mice. The dynamic range of the AIIAC light response in the Bhlhb4-/- mouse (which lacks DBC(R)s) resembles that of the DNQX-resistant component, and that of the connexin36 (Cx36)-/- mouse resembles the DNQX-sensitive component. By comparing the light responses of the DBC(C)s with the DNQX-resistant AIIAC component, and light responses of the DBC(R)s with the DNQX-sensitive AIIAC component, we obtained the input-output relations of the DBC(C)-->AIIAC electrical synapse and the DBC(R)-->AIIAC chemical synapse. Similar to other glutamatergic chemical synapses in the retina, the DBC(R)-->AIIAC synapse is non-linear. Its highest voltage gain (approximately 5) is found near the dark membrane potential, and it saturates for presynaptic signals larger than 5.5 mV. The DBC(C)-->AIIAC electrical synapse is approximately linear (voltage gain of 0.92), consistent with the linear junctional conductance found in retinal electrical synapses. Moreover, relative DBC(R) and DBC(C) contributions to the AIIAC response at various light intensity levels are determined.

Full Text

Duke Authors

Cited Authors

  • Pang, J-J; Abd-El-Barr, MM; Gao, F; Bramblett, DE; Paul, DL; Wu, SM

Published Date

  • April 15, 2007

Published In

Volume / Issue

  • 580 / Pt. 2

Start / End Page

  • 397 - 410

PubMed ID

  • 17255172

Pubmed Central ID

  • PMC2075551

International Standard Serial Number (ISSN)

  • 0022-3751

Digital Object Identifier (DOI)

  • 10.1113/jphysiol.2006.120790


  • eng

Conference Location

  • England