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PMID: 7603841 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Heterotypic gap junction channels (connexin26-connexin32) violate the paradigm of unitary conductance.

Pflugers Archiv : European journal of physiology ·Vol. 429 ·No. 6 ·1995-04-00 ·Pages 870-2

Bukauskas FF, Elfgang C, Willecke K, Weingart R

Abstract

Human HeLa cells transfected with mouse DNA coding for connexin26 (Cx26) or connexin32 (Cx32) were used to examine the properties of heterotypic Cx26-Cx32 gap junction channels. Intercellular current flow was examined in induced cell pairs by means of the dual voltage-clamp method. We found that Cx26-Cx32 channels exhibit voltage-dependent conductances, gamma j: gamma j(main state) increases with increasing positivity at the cytoplasmic aspect of the Cx26 connexon and decreases with increasing negativity (slope: 32 pS/100 mV; gamma j(main state) reaches 48 pS as Vj approaches 0 mV); gamma j(residual state) with a similar Vj-dependence is present when the cytoplasmic end of Cx26 connexon is positive, but absent when it is negative. The single channel data provide an explanation for the asymmetric relationships between the gap junction conductance, gj, and Vj. The results are consistent with the notion that docking of two connexons co-determines the biophysical properties of a gap junction channel.

MeSH Terms
Animals Connexin 26 Connexins/genetics,physiology Electric Conductivity Gap Junctions/physiology HeLa Cells Humans Mice Transfection
Chemicals
Connexins GJB2 protein, human connexin 32 Connexin 26
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bukauskas F F
Physiologisches Institut, Universität Bern, Switzerland.
Elfgang C
Willecke K
Weingart R
References (7)
7 references, click to expand
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Article Info
Journal
Pflugers Archiv : European journal of physiology
Abbr.
Pflugers Arch
ISSN
0031-6768
Published
1995-04-00
Pages
870-2
Language
English
Region
Germany
NLM ID
0154720
Subset
IM
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