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  HCN channels are expressed differentially in retinal bipolar cells and concentrated at synaptic terminals

Müller, F., Scholten, A., Ivanova, E., Haverkamp, S., Kremmer, E., & Kaupp, U. B. (2003). HCN channels are expressed differentially in retinal bipolar cells and concentrated at synaptic terminals. European Journal of Neuroscience, 17(10), 2084-2096.

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 Creators:
Müller, F.1, Author           
Scholten, A., Author
Ivanova, E.2, Author           
Haverkamp, S.3, Author           
Kremmer, E., Author
Kaupp, U. B., Author
Affiliations:
1Neurochemistry Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461704              
2Neuroanatomy Department, Max Planck Institute for Brain Research, Max Planck Society, ou_2461703              
3Neuroanatomical studies on retinal circuitry and synaptic mechanisms Group, Max Planck Institute for Brain Research, Max Planck Society, ou_2461702              

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Free keywords: bipolar cell, electrophysiology, HCN channels, I-h, immunocytochemistry, retina
 Abstract: Hyperpolarization-activated and cyclic nucleotide-gated (HCN) channels codetermine the integrative behaviour of neurons and shape their response to synaptic stimulation. We used immunohistochemistry and patch-clamp recording to study the composition and distribution of HCN channels in the rat retina. All four HCN channel isoforms (HCN1-4) are expressed differentially in the retina. In particular, different classes of bipolar cells have a different inventory of HCN channels. We found no evidence for the formation of heterooligomeric HCN channels. HCN channels are densely clustered at synaptic terminals of bipolar cells and photoreceptors. This suggests that HCN channels are involved in the control of transmitter release.

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Language(s): eng - English
 Dates: 2003
 Publication Status: Issued
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: eDoc: 64984
ISI: 000183481500011
 Degree: -

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Title: European Journal of Neuroscience
  Alternative Title : Eur. J. Neurosci.
Source Genre: Journal
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Pages: - Volume / Issue: 17 (10) Sequence Number: - Start / End Page: 2084 - 2096 Identifier: ISSN: 0953-816X