Literature DB >> 8938732

Xenopus laevis oocytes contain endogenous large conductance Ca2(+)-activated K+ channels.

J D Krause1, C D Foster, P H Reinhart.   

Abstract

Xenopus laevis oocytes have become a pre-eminent tool for studying cloned ion channels, primarily because they intrinsically express low levels of most types of ion channels. However, when these cells are used for single channel studies, it is essential to determine whether or not oocytes contain even low levels of endogenous ion channels with properties similar to the channel being investigated. We show here that X. laevis oocytes express endogenous large-conductance Ca2(+)-activated K+ channels with properties similar to mammalian isoforms of this channel. The endogenous channels exhibit a voltage-dependence of 12-14 mV per e-fold change in open probability (po), can be activated by micromolar Ca2+ concentrations, and have a single channel conductance of approximately 200 pS in symmetrical 110 mM K+ solutions. Patch clamp experiments indicate that this endogenous channel is present at low densities (approximately 1 channel/3000 microns2). If endogenous channel subunits can form functional tetramers with other exogenous potassium channel subunits, then they will give rise to the expression of a heterogeneous channel population. Therefore, studies involving the heterologous expression of large-conductance Ca2(+)-activated K+ channels in Xenopus laevis oocytes require careful analysis and interpretation.

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Year:  1996        PMID: 8938732     DOI: 10.1016/0028-3908(96)00134-7

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  11 in total

1.  Ca2+-dependent gating mechanisms for dSlo, a large-conductance Ca2+-activated K+ (BK) channel.

Authors:  B L Moss; S D Silberberg; C M Nimigean; K L Magleby
Journal:  Biophys J       Date:  1999-06       Impact factor: 4.033

2.  Neuronal fast activating and meningeal silent modulatory BK channel splice variants cloned from rat.

Authors:  Asser Nyander Poulsen; Inger Jansen-Olesen; Jes Olesen; Dan Arne Klaerke
Journal:  Pflugers Arch       Date:  2010-10-12       Impact factor: 3.657

3.  Redox modulation of hslo Ca2+-activated K+ channels.

Authors:  T J DiChiara; P H Reinhart
Journal:  J Neurosci       Date:  1997-07-01       Impact factor: 6.167

4.  Probing the geometry of the inner vestibule of BK channels with sugars.

Authors:  Tinatin I Brelidze; Karl L Magleby
Journal:  J Gen Physiol       Date:  2005-08       Impact factor: 4.086

5.  Gating and conductance properties of BK channels are modulated by the S9-S10 tail domain of the alpha subunit. A study of mSlo1 and mSlo3 wild-type and chimeric channels.

Authors:  B L Moss; K L Magleby
Journal:  J Gen Physiol       Date:  2001-12       Impact factor: 4.086

6.  Slo1 tail domains, but not the Ca2+ bowl, are required for the beta 1 subunit to increase the apparent Ca2+ sensitivity of BK channels.

Authors:  Xiang Qian; Crina M Nimigean; Xiaowei Niu; Brenda L Moss; Karl L Magleby
Journal:  J Gen Physiol       Date:  2002-12       Impact factor: 4.086

7.  Characterization of the human fMLP receptor in neutrophils and in Xenopus oocytes.

Authors:  Sigrid Wittmann; Dieter Fröhlich; Stephen Daniels
Journal:  Br J Pharmacol       Date:  2002-03       Impact factor: 8.739

Review 8.  Molecular mechanisms of BK channel activation.

Authors:  J Cui; H Yang; U S Lee
Journal:  Cell Mol Life Sci       Date:  2009-03       Impact factor: 9.261

9.  Beta1 subunits facilitate gating of BK channels by acting through the Ca2+, but not the Mg2+, activating mechanisms.

Authors:  Xiang Qian; Karl L Magleby
Journal:  Proc Natl Acad Sci U S A       Date:  2003-07-31       Impact factor: 11.205

10.  Protons block BK channels by competitive inhibition with K+ and contribute to the limits of unitary currents at high voltages.

Authors:  Tinatin I Brelidze; Karl L Magleby
Journal:  J Gen Physiol       Date:  2004-03       Impact factor: 4.086

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