| Literature DB >> 15282340 |
Karen Maass1, Alexander Ghanem, Jung-Sun Kim, Manuela Saathoff, Stephanie Urschel, Gregor Kirfel, Ruth Grümmer, Markus Kretz, Thorsten Lewalter, Klaus Tiemann, Elke Winterhager, Volker Herzog, Klaus Willecke.
Abstract
More than 97% of mice in which the C-terminal region of connexin43 (Cx43) was removed (designated as Cx43K258stop) die shortly after birth due to a defect of the epidermal barrier. The abnormal expression of Cx43K258stop protein in the uppermost layers of the epidermis seems to perturb terminal differentiation of keratinocytes. In contrast to Cx43-deficient mice, neonatal Cx43K258stop hearts show no lethal obstruction of the right ventricular outflow tract, but signs of dilatation. Electrocardiographies of neonatal hearts reveal repolarization abnormalities in 20% of homozygous Cx43K258stop animals. The very rare adult Cx43K258stop mice show a compensation of the epidermal barrier defect but persisting impairment of cardiac function in echocardiography. Female Cx43K258stop mice are infertile due to impaired folliculogenesis. Our results indicate that the C-terminally truncated Cx43K258stop mice lack essential functions of Cx43, although the truncated Cx43 protein can form open gap junctional channels.Entities:
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Year: 2004 PMID: 15282340 PMCID: PMC519152 DOI: 10.1091/mbc.e04-04-0324
Source DB: PubMed Journal: Mol Biol Cell ISSN: 1059-1524 Impact factor: 4.138