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From the Departments of Pharmacology (H.G., J.F.E.-V., M.D.) and Microbiology and Immunology (S.M.T.), SUNY Upstate Medical University, Syracuse NY.
Correspondence to Mario Delmar, MD, PhD, Department of Pharmacology, 766 Irving Ave, Syracuse NY 13210. E-mail delmarm{at}mail.upstate.edu
AbstractGap junctions are formed
by oligomerization of a protein called connexin. Most cells express
more than one connexin isotype. Atrial myocytes, for example, coexpress
connexin (Cx) 40 and Cx43. The consequence of connexin coexpression on
the regulation of gap junctions is not well understood. In the
present study, we show that cells coexpressing Cx40 and Cx43 are
more susceptible to acidification-induced uncoupling than those cells
expressing only one connexin isotype. Xenopus oocytes
were injected with mRNA for Cx40, Cx43, or a combination of both.
Intracellular pH and junctional conductance were
simultaneously measured while cells were progressively
acidified by superfusion with a bicarbonate-buffered solution gassed
with increasing concentrations of carbon dioxide. The data show that
the pKa (ie, the pH at which junctional conductance decreased to 50%
from maximum) shifted from
6.7 when cells expressed only Cx40 or
only Cx43 to
7.0 when one of the oocytes was coexpressing both
connexins. Truncation of the carboxyl terminal domains of the connexins
caused the loss of pH sensitivity even after coexpression. The data are
interpreted on the basis of previous studies from our laboratory that
demonstrated heterodomain interactions in the regulation of Cx40 and
Cx43 gap junctions. The possible implications of these findings on the
regulation of native gap junctions that express both connexins remain
to be determined. The full text of this article is available at
http://www.circresaha.org.
Key Words: connexin gap junctions pHi
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