Targeted mutation of plakoglobin in mice reveals essential functions of desmosomes in the embryonic heart

被引:271
作者
Ruiz, P
Brinkmann, V
Ledermann, B
Behrend, M
Grund, C
Thalhammer, C
Vogel, F
Birchmeier, C
Gunthert, U
Franke, WW
Birchmeier, W
机构
[1] SANDOZ PHARMA AG,PRECLIN RES,CH-4002 BASEL,SWITZERLAND
[2] HUMBOLDT UNIV BERLIN,FRANZ VOLHARD CLIN,BERLIN,GERMANY
[3] BASEL INST IMMUNOL,BASEL,SWITZERLAND
[4] GERMAN CANC RES CTR,D-6900 HEIDELBERG,GERMANY
关键词
D O I
10.1083/jcb.135.1.215
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Plakoglobin (gamma-catenin), a member of the armadillo family of proteins, is a constituent of the cytoplasmic plaque of desmosomes, as well as of other adhering cell junctions, and is involved in anchorage of cytoskeletal filaments to specific cadherins. We have generated a null mutation of the plakoglobin gene in mice. Homozygous -/- mutant animals die between days 12-16 of embryogenesis due to defects in heart function. Often, heart ventricles burst and blood floods the pericard. This tissue instability correlates with the absence of desmosomes in heart, but not in epithelial organs. Instead, extended adherens junctions are formed in the heart, which contain desmosomal proteins, i.e., desmoplakin. Thus, plakoglobin is an essential component of myocardiac desmosomes and seems to play a crucial role in the sorting out of desmosomal and adherens junction components, and consequently in the architecture of intercalated discs and the stabilization of heart tissue.
引用
收藏
页码:215 / 225
页数:11
相关论文
共 83 条
  • [1] THE HUMAN PLAKOGLOBIN GENE LOCALIZES ON CHROMOSOME 17Q21 AND IS SUBJECTED TO LOSS OF HETEROZYGOSITY IN BREAST AND OVARIAN CANCERS
    ABERLE, H
    BIERKAMP, C
    TORCHARD, D
    SEROVA, O
    WAGNER, T
    NATT, E
    WIRSCHING, J
    HEIDKAMPER, C
    MONTAGNA, M
    LYNCH, HT
    LENOIR, GM
    SCHERER, G
    FEUNTEUN, J
    KEMLER, R
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (14) : 6384 - 6388
  • [2] ABERLE H, 1994, J CELL SCI, V107, P3655
  • [3] AUTOANTIBODIES AGAINST A NOVEL EPITHELIAL CADHERIN IN PEMPHIGUS-VULGARIS, A DISEASE OF CELL-ADHESION
    AMAGAI, M
    KLAUSKOVTUN, V
    STANLEY, JR
    [J]. CELL, 1991, 67 (05) : 869 - 877
  • [4] ATHERTON BT, 1986, J CELL SCI, V86, P233
  • [5] Functional interaction of beta-catenin with the transcription factor LEF-1
    Behrens, J
    vonKries, JP
    Kuhl, M
    Bruhn, L
    Wedlich, D
    Grosschedl, R
    Birchmeier, W
    [J]. NATURE, 1996, 382 (6592) : 638 - 642
  • [6] LOSS OF EPITHELIAL DIFFERENTIATION AND GAIN OF INVASIVENESS CORRELATES WITH TYROSINE PHOSPHORYLATION OF THE E-CADHERIN BETA-CATENIN COMPLEX IN CELLS TRANSFORMED WITH A TEMPERATURE-SENSITIVE V-SRC GENE
    BEHRENS, J
    VAKAET, L
    FRIIS, R
    WINTERHAGER, E
    VANROY, F
    MAREEL, MM
    BIRCHMEIER, W
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 120 (03) : 757 - 766
  • [7] A new member of the frizzled family from Drosophila functions as a Wingless receptor
    Bhanot, P
    Brink, M
    Samos, CH
    Hsieh, JC
    Wang, YS
    Macke, JP
    Andrew, D
    Nathans, J
    Nusse, R
    [J]. NATURE, 1996, 382 (6588) : 225 - 230
  • [8] EXPRESSION OF WNT-1 IN PC12 CELLS RESULTS IN MODULATION OF PLAKOGLOBIN AND E-CADHERIN AND INCREASED CELLULAR ADHESION
    BRADLEY, RS
    COWIN, P
    BROWN, AMC
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 123 (06) : 1857 - 1865
  • [9] STRUCTURAL-CHANGES AT CARDIAC CELL-JUNCTIONS DURING ISCHEMIA
    BULLOCK, GR
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1986, 18 : 1 - 5
  • [10] NOMENCLATURE OF THE DESMOSOMAL CADHERINS
    BUXTON, RS
    COWIN, P
    FRANKE, WW
    GARROD, DR
    GREEN, KJ
    KING, IA
    KOCH, PJ
    MAGEE, AI
    REES, DA
    STANLEY, JR
    STEINBERG, MS
    [J]. JOURNAL OF CELL BIOLOGY, 1993, 121 (03) : 481 - 483