Giorelli Maurizio, Livrea Paolo, Trojano Maria
Department of Neurologic and Psychiatric Sciences, University of Bari, Bari, Italy.
J Interferon Cytokine Res. 2005 Jul;25(7):395-406. doi: 10.1089/jir.2005.25.395.
The neurotransmitter dopamine counteracts T cell functions through its specific receptor subtype D5R but favors T cell proliferation and adhesion when acting on D3R. We found diminished mRNA and protein levels of D5R, but not of D3R, in peripheral blood mononuclear cells (PBMCs) from untreated multiple sclerosis (MS) patients. Dopamine reduced T cell proliferation, secretion of interferon-gamma (IFN-gamma), and production of matrix metalloproteinase-9 (MMP-9) mRNA in PBMCs from controls but not from MS patients. By contrast, reduced levels of D3R and renewed dopamine-associated regulatory functions were found in PBMCs from IFN-beta treated MS patients. Failure of the dopaminergic system of lymphocytes may lessen the threshold of T cell activation and sustain the pathogenic cascade of MS.
神经递质多巴胺通过其特定受体亚型D5R对抗T细胞功能,但作用于D3R时则有利于T细胞增殖和黏附。我们发现,未经治疗的多发性硬化症(MS)患者外周血单个核细胞(PBMC)中D5R的mRNA和蛋白水平降低,而D3R则未降低。多巴胺可降低对照组PBMC中T细胞的增殖、γ-干扰素(IFN-γ)的分泌以及基质金属蛋白酶-9(MMP-9)mRNA的产生,但对MS患者的PBMC无此作用。相比之下,接受IFN-β治疗的MS患者的PBMC中D3R水平降低,且多巴胺相关调节功能恢复。淋巴细胞多巴胺能系统功能失调可能会降低T细胞活化阈值,并维持MS的致病级联反应。