The cataract causing Cx50-S50P mutant inhibits Cx43 and intercellular communication in the lens epithelium
Experimental cell research, 2009•Elsevier
Mutations in Connexin50 (Cx50) cause cataracts in both humans and mice. The mechanism
(s) behind how mutated connexins lead to a variety of cataracts have yet to be fully
elucidated. Here, we tested whether the cataract inducing Cx50-S50P mutant interacts with
wild-type Connexin43 (Cx43) to form mixed channels with attenuated function. Using dual
whole-cell voltage clamp, immunofluorescent microscopy and in situ dye transfer analysis
we identified a unique interaction between the mutant subunit and wild-type Cx43. In paired …
(s) behind how mutated connexins lead to a variety of cataracts have yet to be fully
elucidated. Here, we tested whether the cataract inducing Cx50-S50P mutant interacts with
wild-type Connexin43 (Cx43) to form mixed channels with attenuated function. Using dual
whole-cell voltage clamp, immunofluorescent microscopy and in situ dye transfer analysis
we identified a unique interaction between the mutant subunit and wild-type Cx43. In paired …
Mutations in Connexin50 (Cx50) cause cataracts in both humans and mice. The mechanism(s) behind how mutated connexins lead to a variety of cataracts have yet to be fully elucidated. Here, we tested whether the cataract inducing Cx50-S50P mutant interacts with wild-type Connexin43 (Cx43) to form mixed channels with attenuated function. Using dual whole-cell voltage clamp, immunofluorescent microscopy and in situ dye transfer analysis we identified a unique interaction between the mutant subunit and wild-type Cx43. In paired Xenopus oocytes, co-expression of Cx50-S50P with Cx43 reduced electrical coupling ≥90%, without a reduction in protein expression. In transfected cells, Cx50-S50P did not target to cell–cell interfaces by itself, but co-expression of Cx50-S50P with Cx43 resulted in its localization at areas of cell–cell contact. We used Cx43 conditional knockout, Cx50 knockout and Cx50-S50P mutant mice to examine this interaction in vivo. Mice expressing both Cx43 and Cx50-S50P in the lens epithelium revealed a unique expression pattern for Cx43 and a reduction in Cx43 protein. In situ dye transfer experiments showed that the Cx50-S50P mutant, but not the Cx50, or Cx43 conditional knockout, greatly inhibited epithelial cell gap junctional communication in a manner similar to a double knockout of Cx43 and Cx50. The inhibitory affects of Cx50-S50P lead to diminished electrical coupling in vitro, as well as a discernable reduction in epithelial cell dye permeation. These data suggest that dominant inhibition of Cx43 mediated epithelial cell coupling may play a role in the lens pathophysiology caused by the Cx50-S50P mutation.
Elsevier