Interactions of connexins with other membrane channels and transporters

被引:44
作者
Chanson, Marc
Kotsias, Basilio A.
Peracchia, Camillo
O'Grady, Scott M.
机构
[1] Univ Minnesota, Dept Physiol, St Paul, MN 55108 USA
[2] Univ Hosp Geneva, Dept Pediat, Geneva, Switzerland
[3] Univ Buenos Aires, Inst Invest Med Alfredo Lanari, RA-1053 Buenos Aires, DF, Argentina
[4] Univ Rochester, Sch Med, Dept Physiol & Pharmacol, Rochester, NY 14642 USA
关键词
CFTR; aquaporin; glutamate receptors; pannexin;
D O I
10.1016/j.pbiomolbio.2007.03.002
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
Cell-to-cell communication through gap junctions exists in most animal cells and is essential for many important biological processes including rapid transmission of electric signals to coordinate contraction of cardiac and smooth muscle, the intercellular propagation of Ca2+ waves and synchronization of physiological processes between adjacent cells within a tissue. Recent studies have shown that connexins (Cx) can have either direct or indirect interactions with other plasma membrane ion channels or membrane transport proteins with important functional consequences. For example, in tissues most severely affected by cystic fibrosis (CF), activation of the CF Transmembrane Conductance Regulator (CFTR) has been shown to influence connexin function. Moreover, a direct interaction between Cx45.6 and the Major Intrinsic Protein/AQPO in lens appears to influence the process of cell differentiation whereas interactions between aquaporin 4 (AQP4) and Cx43 in mouse astrocytes may coordinate the intercellular movement of ions and water between astrocytes. In this review, we discuss evidence supporting interactions between Cx and membrane channels/transporters including CFTR, aquaporins, ionotropic glutamate receptors, and between pannexinl, another class of putative gapjunction-forming proteins, and Kv beta 3, a regulatory beta-subunit of voltage gated potassium channels. Although the precise molecular nature of these interactions has yet to be defined, their consequences may be critical for normal tissue homeostasis. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:233 / 244
页数:12
相关论文
共 82 条
  • [1] Erythrocyte membrane ATP binding cassette (ABC) proteins: MRP1 and CFTR as well as CD39 (ecto-apyrase) involved in RBC ATP transport and elevated blood plasma ATP of cystic fibrosis
    Abraham, EH
    Sterling, KM
    Kim, RJ
    Salikhova, AY
    Huffman, HB
    Crockett, MA
    Johnston, N
    Parker, HW
    Boyle, WE
    Hartov, A
    Demidenko, E
    Efird, J
    Kahn, J
    Grubman, SA
    Jefferson, DM
    Robson, SC
    Thakar, JH
    Lorico, A
    Rappa, G
    Sartorelli, AC
    Okunieff, P
    [J]. BLOOD CELLS MOLECULES AND DISEASES, 2001, 27 (01) : 165 - 180
  • [2] Lens structure in MIP-deficient mice
    Al-Ghoul, KJ
    Kirk, T
    Kuszak, AJ
    Zoltoski, RK
    Shiels, A
    Kuszak, JR
    [J]. ANATOMICAL RECORD PART A-DISCOVERIES IN MOLECULAR CELLULAR AND EVOLUTIONARY BIOLOGY, 2003, 273A (02): : 714 - 730
  • [3] NMDA receptors regulate developmental gap junction uncoupling via CREB signaling
    Arumugam, H
    Liu, XH
    Colombo, PJ
    Corriveau, RA
    Belousov, AB
    [J]. NATURE NEUROSCIENCE, 2005, 8 (12) : 1720 - 1726
  • [4] Ionic currents in multidrug resistant K562 human leukemic cells
    Assef, YA
    Cavarra, SM
    Damiano, AE
    Ibarra, C
    Kotsias, BA
    [J]. LEUKEMIA RESEARCH, 2005, 29 (09) : 1039 - 1047
  • [5] ASSEF YA, 2003, AM J PHYSIOL, V285, pC470
  • [6] The mammalian pannexin family is homologous to the invertebrate innexin gap junction proteins
    Baranova, A
    Ivanova, DV
    Petrash, N
    Pestova, A
    Skoblov, M
    Kelmanson, I
    Shagin, D
    Nazarenko, S
    Geraymovych, E
    Litvin, O
    Tiunova, A
    Born, TL
    Usman, N
    Staroverov, D
    Lukyanov, S
    Panchin, Y
    [J]. GENOMICS, 2004, 83 (04) : 706 - 716
  • [7] Cell-cell communication beyond connexins: The pannexin channels
    Barbe, MT
    Monyer, H
    Bruzzone, R
    [J]. PHYSIOLOGY, 2006, 21 : 103 - 114
  • [8] Interaction between two adapter proteins, PAG and EBP50:: a possible link between membrane rafts and actin cytoskeleton
    Brdicková, N
    Brdicka, T
    Andera, L
    Spicka, J
    Angelisová, P
    Milgram, SL
    Horejsí, V
    [J]. FEBS LETTERS, 2001, 507 (02) : 133 - 136
  • [9] BREZILLON S, 1997, J BIOL CHEM, V272, P27380
  • [10] Pharmacological properties of homomeric and heteromeric pannexin hemichannels expressed in Xenopus oocytes
    Bruzzone, R
    Barbe, MT
    Jakob, NJ
    Monyer, H
    [J]. JOURNAL OF NEUROCHEMISTRY, 2005, 92 (05) : 1033 - 1043