SPECIFIC MOTIFS IN THE EXTERNAL LOOPS OF CONNEXIN PROTEINS CAN DETERMINE GAP JUNCTION FORMATION BETWEEN CHICK HEART MYOCYTES

被引:106
作者
WARNER, A
CLEMENTS, DK
PARIKH, S
EVANS, WH
DEHAAN, RL
机构
[1] EMORY UNIV,DEPT ANAT & CELL BIOL,ATLANTA,GA 30322
[2] NATL INST MED RES,LONDON NW7 1AA,ENGLAND
[3] UNIV WALES COLL MED,DEPT BIOCHEM MED,CARDIFF CF4 4XN,S GLAM,WALES
来源
JOURNAL OF PHYSIOLOGY-LONDON | 1995年 / 488卷 / 03期
基金
英国惠康基金;
关键词
D O I
10.1113/jphysiol.1995.sp021003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
1. Gap junction formation was compared in the absence and presence of small peptides containing extracellular loop sequences of gap junction (connexin) proteins by measuring the time taken for pairs of spontaneously beating embryonic chick heart myoballs to synchronize beat rates. Test peptides were derived from connexin 32. Non-homologous peptides were used as controls. Control pairs took 42 +/- 0 . 5 min (mean +/- S.E.M.; n = 1088) to synchronize. 2. Connexins 32 and 43, but not 26, were detected in gap junction plaques. The density and distribution of connexin immunolabelling varied between myoballs. 3. Peptides containing conserved motifs from extracellular loops 1 and 2 delayed gap junction formation. The steep portion of the dose-response relation lay between 30 and 300 mu M peptide. 4. In loop 1, the conserved motifs QPG and SHVR were identified as being involved in junction formation. In loop 2, the conserved SRPTEK motif was important. The ability of peptides containing the SRPTEK motif to interfere with the formation of gap junctions was enhanced by amino acids from the putative membrane-spanning region. 5. Peptides from loop 1 and loop 2 were equivalently effective; there was no synergism between them. 6. The inclusion of conserved cysteines in test peptides did not make them more effective in the competition assay.
引用
收藏
页码:721 / 728
页数:8
相关论文
共 17 条
[1]  
BECKER DL, 1995, J CELL SCI, V108, P1455
[2]  
BENNETT MVL, 1991, NEURON, V6, P305, DOI 10.1016/0896-6273(91)90241-Q
[3]  
BOWMAN WC, 1980, TXB PHARM
[4]   CONNEXIN40, A COMPONENT OF GAP-JUNCTIONS IN VASCULAR ENDOTHELIUM, IS RESTRICTED IN ITS ABILITY TO INTERACT WITH OTHER CONNEXINS [J].
BRUZZONE, R ;
HAEFLIGER, JA ;
GIMLICH, RL ;
PAUL, DL .
MOLECULAR BIOLOGY OF THE CELL, 1993, 4 (01) :7-20
[5]   JUNCTIONAL RESISTANCE AND ACTION-POTENTIAL DELAY BETWEEN EMBRYONIC HEART CELL AGGREGATES [J].
CLAPHAM, DE ;
SHRIER, A ;
DEHAAN, RL .
JOURNAL OF GENERAL PHYSIOLOGY, 1980, 75 (06) :633-654
[6]   ATTEMPTS TO DEFINE FUNCTIONAL DOMAINS OF GAP JUNCTION PROTEINS WITH SYNTHETIC PEPTIDES [J].
DAHL, G ;
NONNER, W ;
WERNER, R .
BIOPHYSICAL JOURNAL, 1994, 67 (05) :1816-1822
[7]   MUTATIONAL ANALYSIS OF GAP JUNCTION FORMATION [J].
DAHL, G ;
WERNER, R ;
LEVINE, E ;
RABADANDIEHL, C .
BIOPHYSICAL JOURNAL, 1992, 62 (01) :172-182
[8]  
DEHAAN RL, 1995, PROG CELL R, V4, P187
[9]  
HARFST E, 1990, J CELL SCI, V96, P591
[10]  
Kumar N M, 1992, Semin Cell Biol, V3, P3