Santini Emanuela, Alcacer Cristina, Cacciatore Silvia, Heiman Myriam, Hervé Denis, Greengard Paul, Girault Jean-Antoine, Valjent Emmanuel, Fisone Gilberto
Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
J Neurochem. 2009 Feb;108(3):621-33. doi: 10.1111/j.1471-4159.2008.05831.x.
In the dopamine-depleted striatum, extracellular signal-regulated kinase (ERK) signaling is implicated in the development of L-DOPA-induced dyskinesia. To gain insights on its role in this disorder, we examined the effects of L-DOPA on the state of phosphorylation of ERK and downstream target proteins in striatopallidal and striatonigral medium spiny neurons (MSNs). For this purpose, we employed mice expressing enhanced green fluorescent protein (EGFP) under the control of the promoters for the dopamine D(2) receptor (Drd2-EGFP mice) or the dopamine D(1) receptor (Drd1a-EGFP mice), which are expressed in striatopallidal and striatonigral MSNs, respectively. In 6-hydroxydopamine-lesioned Drd2-EGFP mice, L-DOPA increased the phosphorylation of ERK, mitogen- and stress-activated kinase 1 and histone H3, selectively in EGFP-negative MSNs. Conversely, a complete co-localization between EGFP and these phosphoproteins was observed in Drd1a-EGFP mice. The effect of L-DOPA was prevented by blockade of dopamine D(1) receptors. The same pattern of activation of ERK signaling was observed in dyskinetic mice, after repeated administration of L-DOPA. Our results demonstrate that in the dopamine-depleted striatum, L-DOPA activates ERK signaling specifically in striatonigral MSNs. This regulation may result in ERK-dependent changes in striatal plasticity leading to dyskinesia.
在多巴胺耗竭的纹状体中,细胞外信号调节激酶(ERK)信号传导与左旋多巴诱导的运动障碍的发生有关。为了深入了解其在这种疾病中的作用,我们研究了左旋多巴对纹状体苍白球和纹状体黑质中型多棘神经元(MSNs)中ERK及下游靶蛋白磷酸化状态的影响。为此,我们使用了在多巴胺D(2)受体(Drd2-EGFP小鼠)或多巴胺D(1)受体(Drd1a-EGFP小鼠)启动子控制下表达增强型绿色荧光蛋白(EGFP)的小鼠,它们分别在纹状体苍白球和纹状体黑质MSNs中表达。在6-羟基多巴胺损伤的Drd2-EGFP小鼠中,左旋多巴选择性地在EGFP阴性的MSNs中增加了ERK、丝裂原和应激激活激酶1以及组蛋白H3的磷酸化。相反,在Drd1a-EGFP小鼠中观察到EGFP与这些磷酸化蛋白完全共定位。多巴胺D(1)受体的阻断可阻止左旋多巴的作用。在反复给予左旋多巴后的运动障碍小鼠中也观察到了相同模式的ERK信号激活。我们的结果表明,在多巴胺耗竭的纹状体中,左旋多巴特异性地激活纹状体黑质MSNs中的ERK信号传导。这种调节可能导致纹状体可塑性的ERK依赖性变化,从而导致运动障碍。