|
||
Address correspondence to Michael Puljung, 5841 South Maryland Ave., MC6094, Chicago, IL 60637. Fax: (773) 702-6789; email: mpuljung{at}uchicago.edu
Connexins oligomerize to form intercellular channels that gate in response to voltage and chemical agents such as divalent cations. Historically, these are believed to be two independent processes. Here, data for human connexin37 (hCx37) hemichannels indicate that voltage gating can be explained as block/unblock without the necessity for an independent voltage gate. hCx37 hemichannels closed at negative potentials and opened in a time-dependent fashion at positive potentials. In the absence of polyvalent cations, however, the channels were open at relatively negative potentials, passing current linearly with respect to voltage. Current at negative potentials could be inhibited in a concentration-dependent manner by the addition of polyvalent cations to the bathing solution. Inhibition could be explained as voltage-dependent block of hCx37, with the field acting directly on polyvalent cations, driving them through the pore to an intracellular site. At positive potentials, in the presence of polyvalent cations, the field favored polyvalent efflux from the intracellular blocking site, allowing current flow. The rate of appearance of current depended on the species and valence of the polyvalent cation in the bathing solution. The rate of current decay upon repolarization depended on the concentration of polyvalent cations in the bathing solution, consistent with deactivation by polyvalent block, and was rapid (time constants of tens of milliseconds), implying a high local concentration of polyvalents in or near the channel pore. Sustained depolarization slowed deactivation in a flux-dependent, voltage- and time-independent fashion. The model for hCx37 voltage gating as polyvalent block/unblock can be expanded to account for observations in the literature regarding hCx37 gap junction channel behavior.
Key Words: gap junction gating mechanism divalent cation chemical gating voltage-dependent block
This article has been cited by other articles:
![]() |
J. W. Kyle, V. M. Berthoud, J. Kurutz, P. J. Minogue, M. Greenspan, D. A. Hanck, and E. C. Beyer The N Terminus of Connexin37 Contains an {alpha}-Helix That Is Required for Channel Function J. Biol. Chem., July 24, 2009; 284(30): 20418 - 20427. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. L. Harris Gating on the outside J. Gen. Physiol., June 1, 2009; 133(6): 549 - 553. [Full Text] [PDF] |
||||
![]() |
V. K. Verselis, M. P. Trelles, C. Rubinos, T. A. Bargiello, and M. Srinivas Loop Gating of Connexin Hemichannels Involves Movement of Pore-lining Residues in the First Extracellular Loop Domain J. Biol. Chem., February 13, 2009; 284(7): 4484 - 4493. [Abstract] [Full Text] [PDF] |
||||
![]() |
V. K. Verselis and M. Srinivas Divalent Cations Regulate Connexin Hemichannels by Modulating Intrinsic Voltage-dependent Gating J. Gen. Physiol., August 25, 2008; 132(3): 315 - 327. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. W. Kyle, P. J. Minogue, B. C. Thomas, D. A. L. Domowicz, V. M. Berthoud, D. A. Hanck, and E. C. Beyer An intact connexin N-terminus is required for function but not gap junction formation J. Cell Sci., August 15, 2008; 121(16): 2744 - 2750. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Srinivas, D. P. Calderon, J. Kronengold, and V. K. Verselis Regulation of Connexin Hemichannels by Monovalent Cations J. Gen. Physiol., December 27, 2005; 127(1): 67 - 75. [Abstract] [Full Text] [PDF] |
||||
|
|