Guizzetti M, Costa L G
Department of Environmental Health, University of Washington, Seattle 98105-6099, USA.
Neurotoxicology. 2000 Dec;21(6):1117-21.
Activation of cholinergic muscarinic receptors (primarily the M3 subtype) causes proliferation of astroglial cells and this effect is inhibited by low concentrations (10-50 mM) of ethanol. Investigations on the signal transduction pathways activated by muscarinic receptors in a human astrocytoma cell line (1321N1) have focused on protein kinases C (PKC). Among PKC isozymes expressed in this cell line (alpha, epsilon, zeta), the atypical PKCzeta appears to play a primary role in the mitogenic action of muscarinic agonists. We investigated whether activation of these PKC isozymes may be affected by ethanol at concentrations that can inhibit muscarinic receptor-induced proliferation. Carbachol caused an increase in phorbol ester binding and translocation of PKCepsilon, however, these were inhibited only by 100-200 mM ethanol. On the other hand, translocation of the atypical PKCzeta to the perinuclear area by carbachol was inhibited by ethanol in a dose-dependent manner (10-100 mM). These results suggest that activation of PKCzeta may represent a relevant target for the inhibitory effect of ethanol on muscarinic receptor-induced glial cell proliferation.
胆碱能毒蕈碱受体(主要是M3亚型)的激活会导致星形胶质细胞增殖,而低浓度(10 - 50 mM)的乙醇可抑制这种效应。对人星形细胞瘤细胞系(1321N1)中由毒蕈碱受体激活的信号转导途径的研究主要集中在蛋白激酶C(PKC)上。在该细胞系中表达的PKC同工酶(α、ε、ζ)中,非典型PKCζ似乎在毒蕈碱激动剂的促有丝分裂作用中起主要作用。我们研究了这些PKC同工酶的激活是否会受到能抑制毒蕈碱受体诱导增殖的乙醇浓度的影响。卡巴胆碱导致佛波酯结合增加和PKCε易位,然而,这些仅被100 - 200 mM乙醇抑制。另一方面,卡巴胆碱引起的非典型PKCζ向核周区域的易位被乙醇以剂量依赖方式(10 - 100 mM)抑制。这些结果表明,PKCζ的激活可能是乙醇对毒蕈碱受体诱导的胶质细胞增殖抑制作用的一个相关靶点。