Bergquist J, Josefsson E, Tarkowski A, Ekman R, Ewing A
Department of Psychiatry and Neurochemistry, Göteborg University, Sahlgrenska University Hospital, Mölndal, Sweden.
Electrophoresis. 1997 Sep;18(10):1760-6. doi: 10.1002/elps.1150181009.
Single cell analysis with capillary electrophoresis, a technique capable of detecting zeptomole quantities (10(-21) mole) of neurochemical species, has been used to demonstrate that lymphocytes are capable of active synthesis of dopamine and norepinephrine. Exposure of lymphocytes to catecholamines at concentrations as low as 10 nM leads to decreased proliferation and differentiation, e.g. interferon-gamma (IFN-gamma), interleukin-4 (IL-4) and immunoglobulin (Ig). In addition, both inhibition of dopamine uptake with nomifensine and inhibition of packing of catecholamines into vesicles with tetrabenazine, results in significantly lower levels of dopamine and norepinephrine (p < 0.01 and p < 0.05, respectively). The catecholamine-dependent inhibition of T- and B-lymphocyte activity is mediated via an induction of a Bcl-2/Bax and Fas/FasL involved apoptosis. These findings indicate a novel mechanism for regulation of lymphocyte activity in the central nervous system, whereby elevated regional levels of catecholamines might lead to the immunoprivilege of the brain.
采用毛细管电泳进行单细胞分析,该技术能够检测zeptomole数量级(10(-21)摩尔)的神经化学物质,已被用于证明淋巴细胞能够主动合成多巴胺和去甲肾上腺素。淋巴细胞暴露于低至10 nM浓度的儿茶酚胺会导致增殖和分化减少,例如γ干扰素(IFN-γ)、白细胞介素-4(IL-4)和免疫球蛋白(Ig)。此外,用诺米芬辛抑制多巴胺摄取以及用丁苯那嗪抑制儿茶酚胺包装到囊泡中,都会导致多巴胺和去甲肾上腺素水平显著降低(分别为p < 0.01和p < 0.05)。儿茶酚胺依赖性的T和B淋巴细胞活性抑制是通过诱导Bcl-2/Bax和Fas/FasL相关的细胞凋亡介导的。这些发现表明了中枢神经系统中淋巴细胞活性调节的一种新机制,由此儿茶酚胺区域水平升高可能导致大脑的免疫特权。