The molecular basis of selective permeability of connexins is complex and includes both size and charge

被引:99
作者
Nicholson, BJ
Weber, PA
Cao, F
Chang, HC
Lampe, P
Goldberg, G
机构
[1] SUNY Buffalo, Dept Biol Sci, Buffalo, NY 14260 USA
[2] SUNY Buffalo, Dept Chem Engn, Buffalo, NY 14260 USA
[3] Fred Hutchinson Canc Res Ctr, Seattle, WA 98104 USA
关键词
intercellular channels; permeability; channel selectivity; gap junctions;
D O I
10.1590/S0100-879X2000000400002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although gap junction channels are still widely viewed as large, nonspecific pores connecting cells, the diversity in the connexin family has led more attention to be focused on their permeability characteristics. We summarize here the current status of these investigations, both published and on-going, that reveal both charge and size selectivity between gap junction channels composed of different connexins. In particular, this review will focus on quantitative approaches that monitor the expression level of the connexins, so that it is clear that differences that are seen can be attributed to channel properties. The degree of selectivity that is observed is modest compared to other channels, but is likely to be significant for biological molecules that are labile within the cell. Of particular relevance to the in vivo function of gap junctions, recent studies are summarized that demonstrate that the connexin phenotype can control the nature of the endogenous traffic between cells, with consequent effects on biological effects of gap junctions such as tumor suppression.
引用
收藏
页码:369 / 378
页数:10
相关论文
共 46 条
  • [1] Monovalent cation permeation through the connexin40 gap junction channel - Cs, Rb, K, Na, Li, TEA, TMA, TBA, and effects of anions Br, Cl, F, acetate, aspartate, glutamate, and NO3
    Beblo, DA
    Veenstra, RD
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 1997, 109 (04) : 509 - 522
  • [2] Isoform composition of connexin channels determines selectivity among second messengers and uncharged molecules
    Bevans, CG
    Kordel, M
    Rhee, SK
    Harris, AL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (05) : 2808 - 2816
  • [3] BONDI H, 1994, AEROSPACE AM, V32, P5
  • [4] HETEROTYPIC GAP JUNCTION CHANNELS (CONNEXIN26 OR CONNEXIN32) VIOLATE THE PARADIGM OF UNITARY CONDUCTANCE
    BUKAUSKAS, FF
    ELFGANG, C
    WILLECKE, K
    WEINGART, R
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1995, 429 (06): : 870 - 872
  • [5] Cao FL, 1998, J CELL SCI, V111, P31
  • [6] SPECIFIC PERMEABILITY AND SELECTIVE FORMATION OF GAP JUNCTION CHANNELS IN CONNEXIN-TRANSFECTED HELA-CELLS
    ELFGANG, C
    ECKERT, R
    LICHTENBERGFRATE, H
    BUTTERWECK, A
    TRAUB, O
    KLEIN, RA
    HULSER, DF
    WILLECKE, K
    [J]. JOURNAL OF CELL BIOLOGY, 1995, 129 (03) : 805 - 817
  • [7] PERMEABILITY OF THE CELL-TO-CELL MEMBRANE CHANNELS IN MAMMALIAN-CELL JUNCTION
    FLAGGNEWTON, J
    SIMPSON, I
    LOEWENSTEIN, WR
    [J]. SCIENCE, 1979, 205 (4404) : 404 - 407
  • [8] GOLDBERG G, 1999, IN PRESS NATURE CELL
  • [9] GOLDBERG GS, 1995, BIOTECHNIQUES, V18, P490
  • [10] Disruption of alpha(3) connexin gene leads to proteolysis and cataractogenesis in mice
    Gong, XH
    Li, E
    Klier, G
    Huang, QL
    Wu, Y
    Lei, H
    Kumar, NM
    Horwitz, J
    Gilula, NB
    [J]. CELL, 1997, 91 (06) : 833 - 843