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The Kelch‐Like 1 Actin Binding Protein Modulates Neuronal Voltage Gated Calcium Channels
Author(s) -
PiedrasRenteria Erika Sofia,
Perissinotti Paula Patricia,
Ethington Elizabeth Gibbs,
He Yungui,
Martin Jody,
Cribbs Leanne,
Koob Michael D
Publication year - 2013
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.27.1_supplement.913.51
Subject(s) - chemistry , calcium , microbiology and biotechnology , neuroscience , biophysics , calcium channel , voltage dependent calcium channel , cytosol , endocrinology , medicine , biology , biochemistry , enzyme , organic chemistry
Kelch‐like 1 (KLHL1) is a neuronal actin‐binding protein first identified in humans as part of the genetic locus of the neurological movement disorder Spinocerebellar Ataxia type 8. KLHL1 is expressed in the cytosol, axons and dendrites. KLHL1 KO causes loss of post‐synaptic structures, loss of motor coordination and gait abnormalities. KLHL1 is an ion channel modulator and upregulates HVA and LVA calcium currents in vitro by increased recycling endosome activity and by alteration of the kinetics of τ deactivation . We analyzed the endogenous HVA and LVA calcium currents in neurons from WT and KLHL1 KO mice, and compared these data with the acute down‐regulation of KLHL1 using a knock‐down shRNA (KD) strategy. KLHL1 KD caused decreased HVA and LVA calcium current expression. In contrast, the KO had no differences in total LVA current density, yet changes in current kinetics suggest there is a down‐regulation of α 1H and compensatory expression of α 1I . HVA current density was also decreased in KO (40%) at 4–6 DIV but not at 7–10 DIV, suggesting this deficit was also compensated for after 7 DIV. Our data confirm that KLHL1 modulates LVA and HVA channel function in vivo ; the compensatory modulation of currents in the KO may contribute to the mild motor phenotype seen in these mice. This material is based upon work supported by the National Science Foundation under Grant No. 1022075