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Updated: Aug 24, 2026
Patch Clamp Recording of Starburst Amacrine Cells in a Flat-mount Preparation of Deafferentated Mouse Retina
Published on: October 13, 2016
Inward rectifying currents stabilize the membrane potential in dendrites of mouse amacrine cells: patch-clamp
Amane Koizumi1, Tatjana C Jakobs, Richard H Masland
1Howard Hughes Medical Institute, Massachusetts General Hospital, Wellman 429, Boston, MA 02114, USA. akoizumi-ns@umin.ac.jp
Purpose:
To explore the possible existence of inward rectifying currents in the distal dendrites of amacrine cells.
Methods:
Patch-clamp recordings were made from amacrine cells in a new horizontal slice preparation of mouse retina. Single-cell RT-PCR studies were performed after the patch-clamp recordings.
Results:
In contrast to results from vertical slices or dissociated cells, all amacrine cells tested demonstrated inward rectifying currents, IIR. Within the limits of our sample, this current did not depend on the morphological and physiological type of the amacrine cell. Amacrine cells from which the dendrites had been removed did not possess detectable amounts of IIR. Pharmacological experiments with ZD7288 (100 microM) and single-cell RT-PCR from recorded cells revealed that IIR includes an h-current (I(H)) carried by hyperpolarization-activated cyclic nucleotide gated channels (HCN), HCN1 and/or HCN2 subtypes. In the presence of extracellular Cs+ (5 mM), which greatly suppressed IIR, the resting membrane conductance was reduced. IIR suppressed the generation of oscillatory potentials. Intracellular cAMP (8-cpt-cAMP, 1 mM) activated IIR.
Conclusions:
IIR appears to occur within dendrites of many amacrine cells, where it tends to stabilize the resting membrane potential. HCN1 and/or HCN2 channels contribute to IIR in amacrine cells. Dendritic IIR would be expected to contribute to functional independence of the distal dendrites of amacrine cells that express it.
