期刊
BRITISH JOURNAL OF PHARMACOLOGY
卷 153, 期 7, 页码 1474-1484出版社
WILEY
DOI: 10.1038/sj.bjp.0707676
关键词
nicotinic acetylcholine receptor; receptor assembly; receptor targeting; single-channel conductance
资金
- Wellcome Trust Funding Source: Medline
Background and purpose: The aim of this study was to investigate the influence of the intracellular domain of nicotinic acetylcholine receptor ( nAChR) subunits upon receptor assembly, targeting and functional properties. Experimental approach: Because most nAChR subunits form functional receptors only as heteromeric complexes, it can be difficult to examine the influence of individual subunits or subunit domains in isolation. A series of subunit chimaeras was constructed which contain the intracellular loop region ( located between the M3 and M4 transmembrane domains) from nAChR subunits alpha 1-alpha 10 or beta 1-beta 4. All of these chimaeras contain common extracellular and transmembrane domains ( from the nAChR alpha 7 subunit and the 5-hydroxytryptamine receptor 5-HT3A subunit, respectively), thereby facilitating both homomeric receptor assembly and detection with radiolabelled or fluorescent alpha-bungarotoxin. Key results: The nAChR M3-M4 intracellular loop domain had no significant effect upon levels of total subunit protein detected in transfected cells but had a significant influence upon levels of both cell surface and intracellular assembled receptors. Comparisons of functional properties revealed a significant influence of the intracellular loop domain upon both single-channel conductance and receptor desensitization. In addition, studies conducted in polarized epithelial cells demonstrate that the nAChR loop can influence receptor targeting, resulting in either polarized ( apical) or non-polarized distribution. Conclusions and implications: Evidence has been obtained which demonstrates that the large intracellular loop domain of nAChR subunits can exert a profound influence upon receptor assembly, targeting and ion channel properties.
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