Guyon A, Skrzydelski D, Rovère C, Apartis E, Rostène W, Kitabgi P, Mélik Parsadaniantz S, Nahon J L
Institut de Pharmacologie Moléculaire et Cellulaire, UNSA-CNRS UMR 6097, Université de Nice Sophia Antipolis, Sophia Antipolis, Valbonne, France.
Eur J Neurosci. 2008 Sep;28(5):862-70. doi: 10.1111/j.1460-9568.2008.06367.x. Epub 2008 Jul 26.
Dopaminergic neurons of the substantia nigra constitutively express the CXCR4 receptor for the chemokine stromal-cell-derived factor 1alpha (CXCL12) but, to date, no direct effect of CXCR4 activation by CXCL12 on membrane conductance of dopaminergic neurons has been demonstrated. We tested the effects of CXCL12 on whole-cell currents of dopaminergic neurons recorded in patch clamp in substantia nigra slices and showed that CXCL12 (0.01-10 nm) increased the amplitude of total high-voltage-activated (HVA) Ca currents through CXCR4 activation. This effect was reversibly reduced by varpi-conotoxin-GVIA, suggesting that CXCL12 acted on N-type Ca currents, known to be involved in dopamine (DA) release. We therefore investigated the effects of CXCL12 on DA release from cultured dopaminergic neurons from the rat mesencephalon. In basal conditions, CXCL12 alone had no effect on DA release. When neurons were depolarized with KCl (20 mm), and thus when HVA Ca currents were activated, low CXCL12 concentrations (1-50 nm) increased DA release via CXCR4 stimulation. These data strongly suggest that the chemokine CXCL12 can act directly as a neuromodulator of dopaminergic neuronal electrical activity through the modulation of HVA currents.
黑质的多巴胺能神经元组成性地表达趋化因子基质细胞衍生因子1α(CXCL12)的CXCR4受体,但迄今为止,尚未证实CXCL12激活CXCR4对多巴胺能神经元膜电导有直接影响。我们测试了CXCL12对在黑质切片中用膜片钳记录的多巴胺能神经元全细胞电流的影响,结果表明CXCL12(0.01 - 10 nM)通过激活CXCR4增加了总高压激活(HVA)钙电流的幅度。这种效应被ω-芋螺毒素-GVIA可逆性降低,表明CXCL12作用于已知参与多巴胺(DA)释放的N型钙电流。因此,我们研究了CXCL12对大鼠中脑培养的多巴胺能神经元释放DA的影响。在基础条件下,单独的CXCL12对DA释放没有影响。当神经元用氯化钾(20 mM)去极化,从而激活HVA钙电流时,低浓度的CXCL12(1 - 50 nM)通过刺激CXCR4增加DA释放。这些数据强烈表明,趋化因子CXCL12可通过调节HVA电流直接作为多巴胺能神经元电活动的神经调节剂。