The impact of sub-cellular location and intracellular neuronal proteins on properties of GABAA receptors

被引:40
作者
Birnir, Bryndis [1 ]
Korpi, Esa R. [2 ]
机构
[1] Lund Univ, Sch Med, CRC, UMAS, S-20502 Malmo, Sweden
[2] Univ Helsinki, Inst Biomed, Biomedicum, FI-00014 Helsinki, Finland
关键词
D O I
10.2174/138161207782341330
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Most studies of GABA(A) receptor accessory proteins have focused on trafficking, clustering and phosphorylation state of the channel-forming subunits and as a result a number of proteins and mechanisms have been identified that can influence the GABAA channel expression and function in the cell plasma membrane. In the light of a growing list of intracellular and transmembrane neuronal proteins shown to affect the fate, function and pharmacology of the GABAA receptors in neurons, the concept of what constitutes the native GABAA receptor complex may need to be re-examined. It is perhaps more appropriate to consider the associated proteins or some of them to be parts of the receptor channel complex in the capacity of ancillary proteins. Here we highlight some of the effects the intracellular environment has on the GABA-activated channel function and pharmacology. The studies demonstrate the need for co-expression of accessory proteins with the GABAA channel-forming subunits in heterologous expression systems in order to obtain the full repertoire of GABAA receptors characteristics recorded in the native neuronal environment. Further studies e. g. on gene-modified animal models are needed for most of the accessory proteins to establish their significance in normal physiology and in pathophysiology of neurological and psychiatric diseases. The challenge remains to elucidate the effects that the accessory proteins and processes ( e. g. phosphorylation) plus the sub-cellular location have on the "fine-tuning" of the functional and pharmacological properties of the GABAA receptor channels.
引用
收藏
页码:3169 / 3177
页数:9
相关论文
共 136 条
[1]   Gabaa receptor structure-function studies:: A reexamination in light of new acetylcholine receptor structures [J].
Akabas, MH .
INTERNATIONAL REVIEW OF NEUROBIOLOGY, VOL 62, 2004, 62 :1-43
[2]   Neurosteroid access to the GABAA receptor [J].
Akk, G ;
Shu, HJ ;
Wang, C ;
Steinbach, JH ;
Zorumski, CF ;
Covey, DF ;
Mennerick, S .
JOURNAL OF NEUROSCIENCE, 2005, 25 (50) :11605-11613
[3]   Distinct γ2 subunit domains mediate clustering and synaptic function of postsynaptic GABAA receptors and gephyrin [J].
Alldred, MJ ;
Mulder-Rosi, J ;
Lingenfelter, SE ;
Chen, G ;
Lüscher, B .
JOURNAL OF NEUROSCIENCE, 2005, 25 (03) :594-603
[4]  
ANGELOTTI TP, 1993, J NEUROSCI, V13, P1429
[5]   Ion channels and epilepsy [J].
Armijo, JA ;
Shushtarian, M ;
Valdizan, EM ;
Cuadrado, A ;
de las Cuevas, I ;
Adín, J .
CURRENT PHARMACEUTICAL DESIGN, 2005, 11 (15) :1975-2003
[6]   The location of a closed channel gate in the GABAA receptor channel [J].
Bali, Moez ;
Akabas, Myles H. .
JOURNAL OF GENERAL PHYSIOLOGY, 2007, 129 (02) :145-159
[7]   Ligand-gated channels [J].
Barry, PH ;
Lynch, JW .
IEEE TRANSACTIONS ON NANOBIOSCIENCE, 2005, 4 (01) :70-80
[8]   The interaction between stargazin and PSD-95 regulates AMPA receptor surface trafficking [J].
Bats, Cecile ;
Groc, Laurent ;
Choquet, Daniel .
NEURON, 2007, 53 (05) :719-734
[9]   Immunoreactivity for the GABAA receptor α1 subunit, somatostatin and connexin36 distinguishes axoaxonic, basket, and bistratified interneurons of the rat hippocampus [J].
Baude, Agnes ;
Bleasdale, Catherine ;
Dalezios, Yannis ;
Somogyi, Peter ;
Klausberger, Thomas .
CEREBRAL CORTEX, 2007, 17 (09) :2094-2107
[10]   Identification, molecular cloning, and characterization of a novel GABAA receptor-associated protein, GRIF-1 [J].
Beck, M ;
Brickley, K ;
Wilkinson, HL ;
Sharma, S ;
Smith, M ;
Chazot, PL ;
Pollard, S ;
Stephenson, FA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (33) :30079-30090