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Biophys J, January 1999, p. 198-206, Vol. 76, No. 1
*Department of Physiology and Biophysics, Finch University of Health Sciences/The Chicago Medical School, North Chicago, Illinois 60064, and #Department of Pediatrics, University of Chicago, Chicago, Illinois 60637 USA
Lens fiber cells contain two gap junction proteins (Cx56
and Cx45.6 in the chicken). Biochemical studies have suggested that these two proteins can form heteromeric connexons. To investigate the
biophysical properties of heteromeric lens connexons, Cx56 was
co-expressed with Cx45.6 (or its mouse counterpart, Cx50) in
Xenopus oocytes. Whole-cell and single-channel currents
were measured in single oocytes by conventional two-microelectrode voltage-clamp and patch clamp techniques, respectively. Injection of
Cx56 cRNA induced a slowly activating, nonselective cation current that
activated on depolarization to potentials higher than
10 mV. In
contrast, little or no hemichannel current was induced by injection of
Cx50 or Cx45.6 cRNA. Co-expression of Cx56 with Cx45.6 or Cx50 led to a
shift in the threshold for activation to
40 or
70 mV, respectively.
It also slowed the rate of deactivation of the hemichannel currents.
Moreover, an increase in the unitary conductance, steady state
probability of hemichannel opening and mean open times at negative
potentials, was observed in (Cx56 + Cx45.6) cRNA-injected oocytes
compared with Cx56 cRNA-injected oocytes. These results indicate that
co-expression of lens fiber connexins gives rise to novel channels that
may be explained by the formation of heteromeric hemichannels that
contain both connexins.
Biophys J, January 1999, p. 198-206, Vol. 76, No. 1
© 1999 by the Biophysical Society 0006-3495/99/01/198/09 $2.00
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