Egozi Y, Sokolovsky M, Schejter E, Blatt I, Zakut H, Matzkel A, Soreq H
Cell Mol Neurobiol. 1986 Mar;6(1):55-70. doi: 10.1007/BF00742976.
The expression of muscarinic acetylcholine binding sites and of cholinesterases was studied in extracts prepared from discrete regions of the human fetal brain, between the gestational ages of 14 and 24 weeks. The specific binding of [3H]N-methyl-4-piperidyl benzilate [( 4H]-4NMPB) to muscarinic binding sites ranged between 0.05 and 1.30 pmol/mg protein in the different brain regions, with Kd values of 1.2 +/- 0.2 nM. Binding of the cholinergic agonist oxotremorine fitted, in most of the brain regions examined, with a two-site model for the muscarinic binding sites. The density of muscarinic binding sites increased with development in most regions, with different rates and onset times. It was higher by about sixfold in some areas destined to become cholinergic, such as the cortex and midbrain, than in noncholinergic areas such as the cerebellum. In other areas destined to become cholinergic, such as the hippocampus and the caudate putamen, the receptor density remained low. Average density values increased from 0.1 +/- 0.1 at 14 weeks up to 0.7 +/- 0.4 pmol/mg protein at 24 weeks. The variability in the specific activities of cholinesterase was relatively low, and extracts from different brain regions hydrolyzed from 5 to 30 nmol of [3H]acetylcholine/min/mg protein. These were mostly "true" acetylcholinesterase (EC 3.1.1.7) activities, inhibited by 10(-5) M BW284C51, with minor pseudocholinesterase (EC 3.1.1.8) activities, inhibited by 10(-5) M iso-OMPA. The enzyme from different brain regions and developmental stages displayed similar Km values toward [3H]acetylcholine (ca. 4 X 10(-4) M-1). The ontogenetic changes in cholinesterase specific activities had no unifying pattern and/or relationship to the cholinergic nature of the various brain areas. In most of the brain regions, the arbitrary ratio between the specific activity of cholinesterase and the density of muscarinic binding sites decreased with development, with average values and variability ranges of 83 +/- 50 and 19 +/- 19 at 14 and 24 weeks, respectively. Our findings suggest divergent regulation for cholinergic binding sites and cholinesterase in the fetal human brain and imply that the expression of muscarinic receptors is related to the development of cholinergic transmission, while acetylcholinesterase is also involved in other functions in the fetal human brain.
对妊娠14至24周的人胎儿脑不同区域提取物中毒蕈碱型乙酰胆碱结合位点和胆碱酯酶的表达进行了研究。在不同脑区,[3H]N-甲基-4-哌啶基苯甲酸酯([3H]-4NMPB)与毒蕈碱结合位点的特异性结合在0.05至1.30 pmol/mg蛋白质之间,解离常数(Kd)值为1.2±0.2 nM。在所检测的大多数脑区,胆碱能激动剂氧化震颤素的结合符合毒蕈碱结合位点的双位点模型。在大多数区域,毒蕈碱结合位点的密度随发育而增加,速率和起始时间各不相同。在一些注定要成为胆碱能的区域,如皮质和中脑,其密度比非胆碱能区域如小脑高约六倍。在其他注定要成为胆碱能的区域,如海马体和尾状壳核,受体密度仍然较低。平均密度值从14周时的0.1±0.1增加到24周时的0.7±0.4 pmol/mg蛋白质。胆碱酯酶比活性的变异性相对较低,不同脑区提取物每分钟每毫克蛋白质水解5至30 nmol的[3H]乙酰胆碱。这些大多是被10^(-5)M BW284C51抑制的“真正的”乙酰胆碱酯酶(EC 3.1.1.7)活性,以及被10^(-5)M异氟磷抑制的少量假性胆碱酯酶(EC 3.1.1.8)活性。来自不同脑区和发育阶段的酶对[3H]乙酰胆碱的米氏常数(Km)值相似(约4×10^(-4)M^(-1))。胆碱酯酶比活性的个体发育变化没有统一的模式和/或与各脑区胆碱能性质的关系。在大多数脑区,胆碱酯酶比活性与毒蕈碱结合位点密度之间的任意比值随发育而降低,14周和24周时的平均值和变异性范围分别为83±50和19±19。我们的研究结果表明,人胎儿脑中胆碱能结合位点和胆碱酯酶受到不同的调节,这意味着毒蕈碱受体的表达与胆碱能传递的发育有关,而乙酰胆碱酯酶也参与人胎儿脑的其他功能。