Defective Epidermal Barrier in Neonatal Mice Lacking the C-Terminal Region of Connexin43

Author:

Maass Karen1,Ghanem Alexander2,Kim Jung-Sun3,Saathoff Manuela4,Urschel Stephanie1,Kirfel Gregor4,Grümmer Ruth5,Kretz Markus1,Lewalter Thorsten2,Tiemann Klaus2,Winterhager Elke5,Herzog Volker4,Willecke Klaus1

Affiliation:

1. Institut für Genetik, Universitaẗ Bonn, D-53117 Bonn, Germany

2. Medizinische Klinik und Poliklinik II, Kardiologie und Pneumologie, Universitaẗ Bonn, D-53105 Bonn, Germany

3. University of Ulsan, College of Medicine, Seoul, Republic of Korea

4. Institut für Zellbiologie, Universitaẗ Bonn, D-53121 Bonn, Germany

5. Medizinische Fakultaẗ der Universitaẗ Duisburg-Essen, D-45122 Essen, Germany

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.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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