Connexin-made channels as pharmacological targets

被引:41
作者
Hervé, JC
Sarrouilhe, D
机构
[1] Univ Poitiers, CNRS, UMR 6187, Equipe Interact & Commun Cellulaires,Fac Sci Fund, F-86022 Poitiers, France
[2] Univ Poitiers, Fac Med & Pharm, Lab Physiol Humaine, F-86022 Poitiers, France
关键词
Gap junctions; connexin; junctional uncoipling;
D O I
10.2174/1381612054021060
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Gap junctions are clusters of intercellular channels that provide morphological support for direct diffusion of ions and low-molecular-weight molecules between adjacent coupled cells. Each gap junction channel is made by docking of two hemichannels or connexons, each formed by assembly of six proteins (connexins). 21 members of the connexin gene family are likely to be expressed in the human genome. These ubiquitous gated channels, allowing rapid intercellular communication and synchronisation of coupled cell activities, play critical roles in many signalling processes, including co-ordinated cardiac and smooth muscle contractions, neuronal excitability, neurotransmitter release, insulin secretion, epithelial electrolyte transport, etc. Mutational alterations in the connexin genes are associated with the occurrence of multiple pathologies, such as peripheral neuropathies, cardiovascular diseases, dermatological diseases, hereditary deafness and cataract. But the neuro- and cardioprotective effects of blocking agents of junctional channels show that closure of these channels may also be beneficial in certain pathological situations. Consequently, modulation of gap junctional intercellular communication is a potential pharmacological target. In contrast to most other membrane channels, no natural toxin or specific inhibitor of junctional channels has been identified yet and most uncoupling agents generally also affect other ionic channels and receptors. Future research, based for example on the recent developments in genetics, may clarify gap junction physiology. This will in turn provide promising perspectives for the development of targeted drugs.
引用
收藏
页码:1941 / 1958
页数:18
相关论文
共 219 条
[31]   Regulation of gap junctional communication by a pro-inflammatory cytokine in cystic fibrosis transmembrane conductance regulator-expressing but not cystic fibrosis airway cells [J].
Chanson, M ;
Berclaz, PY ;
Scerri, I ;
Dudez, T ;
Wernke-Dollries, K ;
Pizurki, L ;
Pavirani, A ;
Fiedler, MA ;
Suter, S .
AMERICAN JOURNAL OF PATHOLOGY, 2001, 158 (05) :1775-1784
[32]   Zinc modulation of hemichannel currents in Xenopus oocytes [J].
Chappell, RL ;
Zakevicius, J ;
Ripps, H .
BIOLOGICAL BULLETIN, 2003, 205 (02) :209-211
[33]   APIGENIN AND TANGERETIN ENHANCE GAP JUNCTIONAL INTERCELLULAR COMMUNICATION IN RAT-LIVER EPITHELIAL-CELLS [J].
CHAUMONTET, C ;
BEX, V ;
GAILLARDSANCHEZ, I ;
SEILLANHEBERDEN, C ;
SUSCHETET, M ;
MARTEL, P .
CARCINOGENESIS, 1994, 15 (10) :2325-2330
[34]   Peptides homologous to extracellular loop motifs of connexin 43 reversibly abolish rhythmic contractile activity in rabbit arteries [J].
Chaytor, AT ;
Evans, WH ;
Griffith, TM .
JOURNAL OF PHYSIOLOGY-LONDON, 1997, 503 (01) :99-110
[35]   Protein half-lives of two subunits of an NMDA receptor-like complex, the 71-kDa glutamate-binding and the 80-kDa CPP-binding protein [J].
Chen, XY ;
Ferrington, DA ;
Bigelow, DJ ;
Michaelis, EK .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 241 (01) :132-135
[36]  
Civitelli R, 1998, J CELL BIOCHEM, V68, P8, DOI 10.1002/(SICI)1097-4644(19980101)68:1<8::AID-JCB2>3.0.CO
[37]  
2-#
[38]   Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death [J].
Cohen-Salmon, M ;
Ott, T ;
Michel, V ;
Hardelin, JP ;
Perfettini, I ;
Eybalin, M ;
Wu, T ;
Marcus, DC ;
Wangemann, P ;
Willecke, K ;
Petit, C .
CURRENT BIOLOGY, 2002, 12 (13) :1106-1111
[39]   K+ currents underlying the action of endothelium-derived hyperpolarizing factor in guinea-pig, rat and human blood vessels [J].
Coleman, HA ;
Tare, M ;
Parkington, HC .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 531 (02) :359-373
[40]   The use of structure-activity relationships and markers of cell toxicity to detect non-genotoxic carcinogens [J].
Combes, RD .
TOXICOLOGY IN VITRO, 2000, 14 (04) :387-399