Transfer of biologically important molecules between cells through gap junction channels

被引:187
作者
Alexander, DB [1 ]
Goldberg, GS [1 ]
机构
[1] SUNY Stony Brook, Dept Physiol & Biophys, Sch Med, Stony Brook, NY 11796 USA
关键词
D O I
10.2174/0929867033456927
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gap junctions are unique intercellular channels that connect the cytoplasm of adjacent cells. They are the only channels that mediate the direct cytoplasmic exchange of small hydrophilic molecules between cells - a process called gap junctional communication. Formed by a family of integral membrane proteins called connexins, gap junctions are dynamic multifunctional complexes that are essential for healthy vertebrate development and physiology. Defects in connexin proteins, and, therefore, in gap junctional communication, are associated with a large variety of pathologies in humans and experimental animals. Thus, knowledge of the molecules that pass through gap junction channels is extremely important. However, aside from some notable cases, the repertoire of biologically important transjunctional molecules remains relatively unexplored. Indeed, the study of the intercellular transfer of endogenous molecules presents formidable challenges. Here we review developments in identifying biologically relevant molecules that pass between cells through gap junction channels.
引用
收藏
页码:2045 / 2058
页数:14
相关论文
共 96 条
  • [1] RAPID AND REVERSIBLE REDUCTION OF JUNCTIONAL PERMEABILITY IN CELLS INFECTED WITH A TEMPERATURE-SENSITIVE MUTANT OF AVIAN-SARCOMA VIRUS
    ATKINSON, MM
    MENKO, AS
    JOHNSON, RG
    SHEPPARD, JR
    SHERIDAN, JD
    [J]. JOURNAL OF CELL BIOLOGY, 1981, 91 (02) : 573 - 578
  • [2] 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
  • [3] CONNEXIN MUTATIONS IN X-LINKED CHARCOT-MARIE-TOOTH DISEASE
    BERGOFFEN, J
    SCHERER, SS
    WANG, S
    SCOTT, MO
    BONE, LJ
    PAUL, DL
    CHEN, K
    LENSCH, MW
    CHANCE, PF
    FISCHBECK, KH
    [J]. SCIENCE, 1993, 262 (5142) : 2039 - 2042
  • [4] Heteromeric connexons formed by the lens connexins, connexin43 and connexin56
    Berthoud, VM
    Montegna, EA
    Atal, N
    Aithal, NH
    Brink, PR
    Beyer, EC
    [J]. EUROPEAN JOURNAL OF CELL BIOLOGY, 2001, 80 (01) : 11 - 19
  • [5] 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
  • [6] Direct high affinity modulation of connexin channel activity by cyclic nucleotides
    Bevans, CG
    Harris, AL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (06) : 3720 - 3725
  • [7] Heteromeric mixing of connexins:: Compatibility of partners and functional consequences
    Beyer, EC
    Gemel, J
    Martínez, A
    Berthoud, VM
    Valiunas, V
    Moreno, AP
    Brink, PR
    [J]. CELL COMMUNICATION AND ADHESION, 2001, 8 (4-6): : 199 - 204
  • [8] CONNEXIN43 - A PROTEIN FROM RAT-HEART HOMOLOGOUS TO A GAP JUNCTION PROTEIN FROM LIVER
    BEYER, EC
    PAUL, DL
    GOODENOUGH, DA
    [J]. JOURNAL OF CELL BIOLOGY, 1987, 105 (06) : 2621 - 2629
  • [9] BOND SL, 1994, CELL GROWTH DIFFER, V5, P179
  • [10] NULL MUTATIONS OF CONNEXIN32 IN PATIENTS WITH X-LINKED CHARCOT-MARIE-TOOTH DISEASE
    BRUZZONE, R
    WHITE, TW
    SCHERER, SS
    FISCHBECK, KH
    PAUL, DL
    [J]. NEURON, 1994, 13 (05) : 1253 - 1260