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缺乏连接蛋白43 C末端区域的新生小鼠的表皮屏障缺陷。

Defective epidermal barrier in neonatal mice lacking the C-terminal region of connexin43.

作者信息

Maass Karen, Ghanem Alexander, Kim Jung-Sun, Saathoff Manuela, Urschel Stephanie, Kirfel Gregor, Grümmer Ruth, Kretz Markus, Lewalter Thorsten, Tiemann Klaus, Winterhager Elke, Herzog Volker, Willecke Klaus

机构信息

Institut für Genetik, Universitat Bonn, D-53117 Bonn, Germany.

出版信息

Mol Biol Cell. 2004 Oct;15(10):4597-608. doi: 10.1091/mbc.e04-04-0324. Epub 2004 Jul 28.

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.

摘要

连接蛋白43(Cx43)的C末端区域被去除的小鼠(命名为Cx43K258stop)中,超过97%在出生后不久因表皮屏障缺陷而死亡。Cx43K258stop蛋白在表皮最上层的异常表达似乎扰乱了角质形成细胞的终末分化。与Cx43缺陷小鼠不同,新生的Cx43K258stop心脏未出现右心室流出道的致命梗阻,但有扩张迹象。新生心脏的心电图显示,20%的纯合Cx43K258stop动物存在复极异常。非常罕见的成年Cx43K258stop小鼠表现出表皮屏障缺陷的代偿,但超声心动图显示心脏功能持续受损。雌性Cx43K258stop小鼠因卵泡发生受损而不育。我们的结果表明,C末端截短的Cx43K258stop小鼠缺乏Cx43的基本功能,尽管截短的Cx43蛋白可以形成开放的间隙连接通道。

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