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Dominant cataracts result from incongruous mixing of wild-type lens connexins
Gap junctions are composed of proteins called connexins (Cx) and facilitate both ionic and biochemical modes of intercellular communication. In the lens, Cx46 and Cx50 provide the gap junctional coupling needed for homeostasis and growth. In mice, deletion of Cx46 produced severe cataracts, whereas...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2003
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172970/ https://www.ncbi.nlm.nih.gov/pubmed/12782682 http://dx.doi.org/10.1083/jcb.200303068 |
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author | Martinez-Wittinghan, Francisco J. Sellitto, Caterina Li, Leping Gong, Xiaohua Brink, Peter R. Mathias, Richard T. White, Thomas W. |
author_facet | Martinez-Wittinghan, Francisco J. Sellitto, Caterina Li, Leping Gong, Xiaohua Brink, Peter R. Mathias, Richard T. White, Thomas W. |
author_sort | Martinez-Wittinghan, Francisco J. |
collection | PubMed |
description | Gap junctions are composed of proteins called connexins (Cx) and facilitate both ionic and biochemical modes of intercellular communication. In the lens, Cx46 and Cx50 provide the gap junctional coupling needed for homeostasis and growth. In mice, deletion of Cx46 produced severe cataracts, whereas knockout of Cx50 resulted in significantly reduced lens growth and milder cataracts. Genetic replacement of Cx50 with Cx46 by knockin rescued clarity but not growth. By mating knockin and knockout mice, we show that heterozygous replacement of Cx50 with Cx46 rescued growth but produced dominant cataracts that resulted from disruption of lens fiber morphology and crystallin precipitation. Impedance measurements revealed normal levels of ionic gap junctional coupling, whereas the passage of fluorescent dyes that mimic biochemical coupling was altered in heterozygous knockin lenses. In addition, double heterozygous knockout lenses retained normal growth and clarity, whereas knockover lenses, where native Cx46 was deleted and homozygously knocked into the Cx50 locus, displayed significantly deficient growth but maintained clarity. Together, these findings suggest that unique biochemical modes of gap junctional communication influence lens clarity and lens growth, and this biochemical coupling is modulated by the connexin composition of the gap junction channels. |
format | Text |
id | pubmed-2172970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21729702008-05-01 Dominant cataracts result from incongruous mixing of wild-type lens connexins Martinez-Wittinghan, Francisco J. Sellitto, Caterina Li, Leping Gong, Xiaohua Brink, Peter R. Mathias, Richard T. White, Thomas W. J Cell Biol Article Gap junctions are composed of proteins called connexins (Cx) and facilitate both ionic and biochemical modes of intercellular communication. In the lens, Cx46 and Cx50 provide the gap junctional coupling needed for homeostasis and growth. In mice, deletion of Cx46 produced severe cataracts, whereas knockout of Cx50 resulted in significantly reduced lens growth and milder cataracts. Genetic replacement of Cx50 with Cx46 by knockin rescued clarity but not growth. By mating knockin and knockout mice, we show that heterozygous replacement of Cx50 with Cx46 rescued growth but produced dominant cataracts that resulted from disruption of lens fiber morphology and crystallin precipitation. Impedance measurements revealed normal levels of ionic gap junctional coupling, whereas the passage of fluorescent dyes that mimic biochemical coupling was altered in heterozygous knockin lenses. In addition, double heterozygous knockout lenses retained normal growth and clarity, whereas knockover lenses, where native Cx46 was deleted and homozygously knocked into the Cx50 locus, displayed significantly deficient growth but maintained clarity. Together, these findings suggest that unique biochemical modes of gap junctional communication influence lens clarity and lens growth, and this biochemical coupling is modulated by the connexin composition of the gap junction channels. The Rockefeller University Press 2003-06-09 /pmc/articles/PMC2172970/ /pubmed/12782682 http://dx.doi.org/10.1083/jcb.200303068 Text en Copyright © 2003, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Martinez-Wittinghan, Francisco J. Sellitto, Caterina Li, Leping Gong, Xiaohua Brink, Peter R. Mathias, Richard T. White, Thomas W. Dominant cataracts result from incongruous mixing of wild-type lens connexins |
title | Dominant cataracts result from incongruous mixing of wild-type lens connexins |
title_full | Dominant cataracts result from incongruous mixing of wild-type lens connexins |
title_fullStr | Dominant cataracts result from incongruous mixing of wild-type lens connexins |
title_full_unstemmed | Dominant cataracts result from incongruous mixing of wild-type lens connexins |
title_short | Dominant cataracts result from incongruous mixing of wild-type lens connexins |
title_sort | dominant cataracts result from incongruous mixing of wild-type lens connexins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2172970/ https://www.ncbi.nlm.nih.gov/pubmed/12782682 http://dx.doi.org/10.1083/jcb.200303068 |
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