Yuan Chunbo, O'Connell Robert J, Wilson Andrew, Pietrzykowski Andrzej Z, Treistman Steven N
Brudnick Neuropsychiatric Research Institute, University of Massachusetts Medical School, Worcester, Massachusetts 01604, USA.
J Biol Chem. 2008 Feb 22;283(8):5090-8. doi: 10.1074/jbc.M708214200. Epub 2007 Dec 15.
Ethanol tolerance, in which exposure leads to reduced sensitivity, is an important component of alcohol abuse and addiction. The molecular mechanisms underlying this process remain poorly understood. The BKCa channel plays a central role in the behavioral response to ethanol in Caenorhabditis elegans (Davies, A. G., Pierce-Shimomura, J. T., Kim, H., VanHoven, M. K., Thiele, T. R., Bonci, A., Bargmann, C. I., and McIntire, S. L. (2003) Cell 115, 655-666) and Drosophila (Cowmeadow, R. B., Krishnan, H. R., and Atkinson, N. S. (2005) Alcohol. Clin. Exp. Res. 29, 1777-1786) . In neurons, ethanol tolerance in BKCa channels has two components: a reduced number of membrane channels and decreased potentiation of the remaining channels (Pietrzykowski, A. Z., Martin, G. E., Puig, S. I., Knott, T. K., Lemos, J. R., and Treistman, S. N. (2004) J. Neurosci. 24, 8322-8332) . Here, heterologous expression coupled with planar bilayer techniques examines two additional aspects of tolerance in human BKCa channels. 1) Is acute tolerance observed in a single channel protein complex within a lipid environment reduced to only two lipids? 2) Does lipid bilayer composition affect the appearance of acute tolerance? We found that tolerance was observable in BKCa channels in membrane patches pulled from HEK cells and when they are placed into reconstituted 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylethanolamine/1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylserine membranes. Furthermore, altering bilayer thickness by incorporating the channel into lipid mixtures of 1,2-dioleoyl-3-phosphatidylethanolamine with phosphatidylcholines of increasing chain length, or with sphingomyelin, strongly affected the sensitivity of the channel, as well as the time course of the acute response. Ethanol sensitivity changed from a strong potentiation in thin bilayers to inhibition in thick sphingomyelin/1,2-dioleoyl-3-phosphatidylethanolamine bilayers. Thus, tolerance can be an intrinsic property of the channel protein-lipid complex, and bilayer thickness plays an important role in shaping the pattern of response to ethanol. As a consequence of these findings the protein-lipid complex should be treated as a unit when studying ethanol action.
乙醇耐受性是酒精滥用和成瘾的一个重要组成部分,在这种情况下,接触乙醇会导致敏感性降低。然而,这一过程背后的分子机制仍知之甚少。大电导钙激活钾通道(BKCa通道)在秀丽隐杆线虫(戴维斯,A.G.,皮尔斯 - 岛村,J.T.,金,H.,范霍文,M.K.,蒂勒,T.R.,博尼,A.,巴格曼,C.I.,和麦金太尔,S.L.(2003年)《细胞》115卷,655 - 666页)和果蝇(考梅多,R.B.,克里希南,H.R.,和阿特金森,N.S.(2005年)《酒精.临床与实验研究》29卷,1777 - 1786页)对乙醇的行为反应中起着核心作用。在神经元中,BKCa通道的乙醇耐受性有两个组成部分:膜通道数量减少以及剩余通道的增强作用减弱(彼得日科夫斯基,A.Z.,马丁,G.E.,皮格,S.I.,诺特,T.K.,莱莫斯,J.R.,和特雷斯特曼,S.N.(2004年)《神经科学杂志》24卷,8322 - 8332页)。在此,通过异源表达结合平面双层技术研究了人类BKCa通道耐受性的另外两个方面。1)在脂质环境中,单个通道蛋白复合物中的急性耐受性是否在仅含两种脂质的情况下就会降低?2)脂质双层组成是否会影响急性耐受性的表现?我们发现,从人胚肾(HEK)细胞中提取的膜片中的BKCa通道以及将其置于重构的1 - 棕榈酰 - 2 - 油酰 - sn - 甘油 - 3 - 磷脂酰乙醇胺/1 - 棕榈酰 - 2 - 油酰 - sn - 甘油 - 3 - 磷脂酰丝氨酸膜中时,耐受性是可观察到的。此外,通过将通道整合到1,2 - 二油酰 - 3 - 磷脂酰乙醇胺与链长增加的磷脂酰胆碱或鞘磷脂的脂质混合物中改变双层厚度,会强烈影响通道的敏感性以及急性反应过程。乙醇敏感性从薄双层中的强烈增强转变为厚鞘磷脂/1,2 - 二油酰 - 3 - 磷脂酰乙醇胺双层中的抑制。因此,耐受性可能是通道蛋白 - 脂质复合物的一种内在特性,并且双层厚度在塑造对乙醇的反应模式中起着重要作用。基于这些发现,在研究乙醇作用时,应将蛋白 - 脂质复合物视为一个整体。