Literature DB >> 15356203

KChIPs and Kv4 alpha subunits as integral components of A-type potassium channels in mammalian brain.

Kenneth J Rhodes1, Karen I Carroll, M Amy Sung, Lisa C Doliveira, Michael M Monaghan, Sharon L Burke, Brian W Strassle, Lynn Buchwalder, Milena Menegola, Jie Cao, W Frank An, James S Trimmer.   

Abstract

Voltage-gated potassium (Kv) channels from the Kv4, or Shal-related, gene family underlie a major component of the A-type potassium current in mammalian central neurons. We recently identified a family of calcium-binding proteins, termed KChIPs (Kv channel interacting proteins), that bind to the cytoplasmic N termini of Kv4 family alpha subunits and modulate their surface density, inactivation kinetics, and rate of recovery from inactivation (An et al., 2000). Here, we used single and double-label immunohistochemistry, together with circumscribed lesions and coimmunoprecipitation analyses, to examine the regional and subcellular distribution of KChIPs1-4 and Kv4 family alpha subunits in adult rat brain. Immunohistochemical staining using KChIP-specific monoclonal antibodies revealed that the KChIP polypeptides are concentrated in neuronal somata and dendrites where their cellular and subcellular distribution overlaps, in an isoform-specific manner, with that of Kv4.2 and Kv4.3. For example, immunoreactivity for KChIP1 and Kv4.3 is concentrated in the somata and dendrites of hippocampal, striatal, and neocortical interneurons. Immunoreactivity for KChIP2, KChIP4, and Kv4.2 is concentrated in the apical and basal dendrites of hippocampal and neocortical pyramidal cells. Double-label immunofluorescence labeling revealed that throughout the forebrain, KChIP2 and KChIP4 are frequently colocalized with Kv4.2, whereas in cortical, hippocampal, and striatal interneurons, KChIP1 is frequently colocalized with Kv4.3. Coimmunoprecipitation analyses confirmed that all KChIPs coassociate with Kv4 alpha subunits in brain membranes, indicating that KChIPs 1-4 are integral components of native A-type Kv channel complexes and are likely to play a major role as modulators of somatodendritic excitability.

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Year:  2004        PMID: 15356203      PMCID: PMC6729940          DOI: 10.1523/JNEUROSCI.0776-04.2004

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  129 in total

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Journal:  J Physiol       Date:  2005-09-01       Impact factor: 5.182

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Authors:  Aaron Lauver; Li-Lian Yuan; Andreas Jeromin; Brian M Nadin; José J Rodríguez; Heather A Davies; Michael G Stewart; Gang-Yi Wu; Paul J Pfaffinger
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Review 6.  Polarized targeting of ion channels in neurons.

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7.  Three-dimensional structure of the KChIP1-Kv4.3 T1 complex reveals a cross-shaped octamer.

Authors:  Marta Pioletti; Felix Findeisen; Greg L Hura; Daniel L Minor
Journal:  Nat Struct Mol Biol       Date:  2006-10-22       Impact factor: 15.369

8.  Kv4 accessory protein DPPX (DPP6) is a critical regulator of membrane excitability in hippocampal CA1 pyramidal neurons.

Authors:  Jinhyun Kim; Marcela S Nadal; Ann M Clemens; Matthew Baron; Sung-Cherl Jung; Yoshio Misumi; Bernardo Rudy; Dax A Hoffman
Journal:  J Neurophysiol       Date:  2008-07-30       Impact factor: 2.714

9.  Tetraethylammonium (TEA) increases the inactivation time constant of the transient K+ current in suprachiasmatic nucleus neurons.

Authors:  Ludovic Alvado; Charles N Allen
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10.  The auxiliary subunit KChIP2 is an essential regulator of homeostatic excitability.

Authors:  Hong-Gang Wang; Xiao Ping He; Qiang Li; Roger D Madison; Scott D Moore; James O McNamara; Geoffrey S Pitt
Journal:  J Biol Chem       Date:  2013-03-27       Impact factor: 5.157

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