BKβ1 Subunits Contribute to BK Channel Diversity in Rat Hypothalamic Neurons

Large conductance Ca²⁺-activated BK channels are important regulators of action potential duration and firing frequency in many neurons. As the pore-forming subunits of BK channels are encoded by a single gene, channel diversity is mainly generated by alternative splicing and interaction with auxili...

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Bibliographic Details
Published in:Cellular and molecular neurobiology 2010-08, Vol.30 (6), p.967-976
Main Authors: Salzmann, Mikhail, Seidel, Katharina N, Bernard, René, Prüss, Harald, Veh, Rüdiger W, Derst, Christian
Format: Article
Language:English
Subjects:
Biomedical and Life Sciences
Biomedicine
Cell Biology
hypothalamus
Ion channel
MaxiK
Ncl. paraventricularis
Ncl. supraopticus
Neurobiology
Neurosciences
Original Research
Slo
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Summary:Large conductance Ca²⁺-activated BK channels are important regulators of action potential duration and firing frequency in many neurons. As the pore-forming subunits of BK channels are encoded by a single gene, channel diversity is mainly generated by alternative splicing and interaction with auxiliary β-subunits (BKβ1-4). In hypothalamic neurons several BK channel subtypes have been described electrophysiologically; however, the distribution of BKβ subunits is unknown so far. Therefore, an antibody against the large extracellular loop of the BKβ1 subunit was raised, freed from cross-reactivity against BKβ2-4 and affinity-purified. The resulting polyclonal monospecific BKβ1 antibody was characterized by Western blot analysis, ELISA techniques and immunocytochemical staining of BKβ1-4-transfected CHO and COS-1 cells. Regional and cellular distribution in the rat hypothalamus was analysed by immunocytochemistry and in situ hybridization experiments. Immunocytochemical staining of rat hypothalamic neurons indicates strong BKβ1 expression in the supraoptic nucleus and the magno- and parvocellular parts of the paraventricular nucleus. Lower expression was found in periventricular nucleus, the arcuate nucleus and in the median eminence. Immunostaining was predominantly localized to somata. In addition, pericytes and ependymal epithelial cells showed BKβ1 labelling. In all cases immunocytochemical results were supported by in situ hybridization.
ISSN:0272-4340
1573-6830
DOI:10.1007/s10571-010-9527-7