Expression and function of connexins in the epidermis, analyzed with transgenic mouse mutants

被引:60
作者
Kretz, M [1 ]
Maass, K [1 ]
Willecke, K [1 ]
机构
[1] Univ Bonn, Inst Genet, Abt Mol Genet, D-53117 Bonn, Germany
关键词
gap junctions; connexin43; epidermal perineability barrier; wound healing;
D O I
10.1078/0171-9335-00422
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Eight different connexins are expressed in mouse epidermis with overlapping expression patterns in different epidermal layers. Analyses of mice with deficiency or modifications of distinct connexins yielded insights into the large variety of connexins in the epidermis. Connexin43 (Cx43) deficiency in mouse epidermis resulted in a significant acceleration of wound closure. Truncation by 125 amino acid residues of the Cx43 C-terminal region led to an altered epidermal expression pattern of Cx43 and defective development of the epidermal water barrier in transgenic mice, although the truncated Cx43 protein could still form open gap junctional channels in transfected HeLa cells. Thus, the phenotypic abnormalities observed in mice with truncated Cx43 protein (Cx43K258Stop) are more likely due to defective regulation of this protein rather than the closed Cx43 channel. Our studies of connexin-deficient mice revealed an extensive redundancy of connexins expressed in mouse epidermis. Epidermal connexins seem to form two functional groups in which deficiency of one connexin isoform can be compensated by other connexin isoforms of the same group.
引用
收藏
页码:647 / 654
页数:8
相关论文
共 59 条
[1]   Post-translational integration and oligomerization of connexin 26 in plasma membranes and evidence of formation of membrane pores: implications for the assembly of gap junctions [J].
Ahmad, S ;
Evans, WH .
BIOCHEMICAL JOURNAL, 2002, 365 (03) :693-699
[2]   Stem cells of the skin epithelium [J].
Alonso, L ;
Fuchs, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 :11830-11835
[3]   Erythrokeratoderma variabilis without connexin 31 or connexin 30.3 gene mutation: Immunohistological, ultrastructural and genetic studies [J].
Arita, K ;
Akiyama, M ;
Tsuji, Y ;
Onozuka, T ;
Shimizu, H .
ACTA DERMATO-VENEREOLOGICA, 2003, 83 (04) :266-270
[4]   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
[5]   Connexins 26, 30, and 43:: Differences among spontaneous, chronic, and accelerated human wound healing [J].
Brandner, JM ;
Houdek, P ;
Hüsing, B ;
Kaiser, C ;
Moll, I .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2004, 122 (05) :1310-1320
[6]   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
[7]  
Budunova IV, 1996, MOL CARCINOGEN, V15, P202
[8]  
Cartlidge P, 2000, Semin Neonatol, V5, P273, DOI 10.1053/siny.2000.0013
[9]   Wound epithelialization: Accelerationg the pace of discovery [J].
Coulombe, PA .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (02) :219-230
[10]   Dynamic changes in connexin expression correlate with key events in the wound healing process [J].
Coutinho, P ;
Qiu, C ;
Frank, S ;
Tamber, K ;
Becker, D .
CELL BIOLOGY INTERNATIONAL, 2003, 27 (07) :525-541