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Am J Physiol Cell Physiol 287: C1596-C1604, 2004. First published July 28, 2004; doi:10.1152/ajpcell.00225.2004
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

Biophysical characterization of zebrafish connexin35 hemichannels

Virginijus Valiunas,1 Rickie Mui,1 Elizabeth McLachlan,2 Gunnar Valdimarsson,2 Peter R. Brink,1 and Thomas W. White1

1Department of Physiology and Biophysics, State University of New York, Stony Brook, New York 11794; and 2Department of Zoology, University of Manitoba, Winnipeg, Canada R3T 2N2

Submitted 6 May 2004 ; accepted in final form 23 July 2004

A subset of connexins can form unopposed hemichannels in expression systems, providing an opportunity for comparison of hemichannel gating properties with those of intact gap junction channels. Zebrafish connexin35 (Cx35) is a member of the Cx35/Cx36 subgroup of connexins highly expressed in the retina and brain. In the present study, we have shown that Cx35 expression in Xenopus oocytes and N2A cells produced large outward whole cell currents on cell depolarization. Using whole cell, cell-attached, and excised patch configurations, we obtained multichannel and single-channel current recordings attributable to the Cx35 hemichannels (Ihc) that were activated and increased by stepwise depolarization of membrane potential (Vm) and deactivated by hyperpolarization. The currents were not detected in untransfected N2A cells or in control oocytes injected with antisense Cx38. However, water-injected oocytes that were not treated with antisense showed activities attributable to Cx38 hemichannels that were easily distinguishable from Cx35 hemichannels by a significantly larger unitary conductance ({gamma}hc: 250–320 pS). The {gamma}hc of Cx35 hemichannels exhibited a pronounced Vm dependence; i.e., {gamma}hc increased/decreased with relative hyperpolarization/depolarization ({gamma}hc was 72 pS at Vm = –100 mV and 35 pS at Vm = 100 mV). Extrapolation to Vm = 0 mV predicted a {gamma}hc of 48 pS, suggesting a unitary conductance of intact Cx35 gap junction channels of ~24 pS. Channel gating was also Vm dependent: open time declined with negative Vm and increased with positive Vm. The ability to break down the complex gating of intact intercellular channels into component hemichannels in vitro will help to evaluate putative physiological roles for hemichannels in vivo.

connexin; gating; retina



Address for reprint requests and other correspondence: T. W. White, Dept. of Physiology and Biophysics, State Univ. of New York, T5-147, Basic Science Tower, Stony Brook, NY 11794-8661 (E-mail: thomas.white{at}sunysb.edu)




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