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

被引:107
作者
Maass, K
Ghanem, A
Kim, JS
Saathoff, M
Urschel, S
Kirfel, G
Grümmer, R
Kretz, M
Lewalter, T
Tiemann, K
Winterhager, E
Herzog, V
Willecke, K [1 ]
机构
[1] Univ Bonn, Inst Genet, D-53117 Bonn, Germany
[2] Univ Bonn, Med Klin & Poliklin 2, D-53105 Bonn, Germany
[3] Univ Ulsan, Coll Med, Seoul, South Korea
[4] Univ Bonn, Inst Zellbiol, D-53121 Bonn, Germany
[5] Univ Essen Gesamthsch, Fak Med, D-45122 Essen, Germany
关键词
D O I
10.1091/mbc.E04-04-0324
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:4597 / 4608
页数:12
相关论文
共 73 条
[1]   Intercellular communication via connexin43 gap junctions is required for ovarian folliculogenesis in the mouse [J].
Ackert, CL ;
Gittens, JEI ;
O'Brien, MJ ;
Eppig, JJ ;
Kidder, GM .
DEVELOPMENTAL BIOLOGY, 2001, 233 (02) :258-270
[2]  
[Anonymous], 1994, MANIPULATING MOUSE E
[3]   Targeted epidermal expression of mutant Connexin 26(D66H) mimics true Vohwinkel syndrome and provides a model for the pathogenesis of dominant connexin disorders [J].
Bakirtzis, G ;
Choudhry, R ;
Aasen, T ;
Shore, L ;
Brown, K ;
Bryson, S ;
Forrow, S ;
Tetley, L ;
Finbow, M ;
Greenhalgh, D ;
Hodgins, M .
HUMAN MOLECULAR GENETICS, 2003, 12 (14) :1737-1744
[4]   Increased association of ZO-1 with connexin43 during remodeling of cardiac gap junctions [J].
Barker, RJ ;
Price, RL ;
Gourdie, RG .
CIRCULATION RESEARCH, 2002, 90 (03) :317-324
[5]   SWITCH IN GAP JUNCTION PROTEIN EXPRESSION IS ASSOCIATED WITH SELECTIVE CHANGES IN JUNCTIONAL PERMEABILITY DURING KERATINOCYTE DIFFERENTIATION [J].
BRISSETTE, JL ;
KUMAR, NM ;
GILULA, NB ;
HALL, JE ;
DOTTO, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6453-6457
[6]  
Cartlidge P, 2000, Semin Neonatol, V5, P273, DOI 10.1053/siny.2000.0013
[7]   Mice lacking desmocollin 1 show epidermal fragility accompanied by barrier defects and abnormal differentiation [J].
Chidgey, M ;
Brakebusch, C ;
Gustafsson, E ;
Cruchley, A ;
Hail, C ;
Kirk, S ;
Merritt, A ;
North, A ;
Tselepis, C ;
Hewitt, J ;
Byrne, C ;
Fassler, R ;
Garrod, D .
JOURNAL OF CELL BIOLOGY, 2001, 155 (05) :821-832
[8]  
Choudhry R, 1997, DEV DYNAM, V210, P417, DOI 10.1002/(SICI)1097-0177(199712)210:4<417::AID-AJA6>3.0.CO
[9]  
2-J
[10]   Identification of connexin43 (α1) gap junction gene mutations in patients with hypoplastic left heart syndrome by denaturing gradient gel electrophoresis (DGGE) [J].
Dasgupta, C ;
Martinez, AM ;
Zuppan, CW ;
Shah, MM ;
Bailey, LL ;
Fletcher, WH .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2001, 479 (1-2) :173-186