Wang Xinsheng, Wiesinger Jason, Beard John, Felt Barbara, Menzies Sharon, Earley Christopher, Allen Richard, Connor James
Department of Neural and Behavioral Science (H109), Penn State College of Medicine, 500 University Drive, Hershey, PA 17033, USA.
J Neurol Sci. 2004 May 15;220(1-2):59-66. doi: 10.1016/j.jns.2004.02.004.
Thy-1 is a cell adhesion molecule that plays a regulatory role in the vesicular release of neurotransmitters. The objective of this study is to examine the relationship between iron status and Thy1 expression in neuronal systems of varying complexity. Pheochromocytoma cell (PC12) cells were used to explore whether there was a direct relation between cellular iron status and Thy1 expression. Iron chelation significantly decreased expression of Thy1 in PC12 cells in a dose and time dependent manner. Transferrin receptor expression was increased with iron chelation demonstrating that a global decrease in protein synthesis could not account for the Thy1 changes. We also examined brain homogenates from adult rats that were nursed by dams on an iron deficient (ID) diet and found a significant decrease in Thy1 compared to control rats. Finally, the substantia nigra from individuals with Restless Legs Syndrome reportedly has lower than normal amounts of iron. Therefore, we examined this brain region from individuals with the clinical diagnosis of primary Restless Legs syndrome (RLS) and found the concentration of Thy1 was less than half that of controls. The results of these studies support the novel concept that there is a relationship between Thy1 and iron and point to a novel mechanism by which iron deficiency can affect brain function. They also indicate a possible mechanism by which iron deficiency compromises dopaminergic transmission in RLS, providing a potentially important link between decreased brain iron and the responsiveness to levodopa and iron supplementation treatment in RLS.
Thy-1是一种细胞粘附分子,在神经递质的囊泡释放中起调节作用。本研究的目的是探讨不同复杂程度神经元系统中铁状态与Thy1表达之间的关系。使用嗜铬细胞瘤细胞(PC12)来探究细胞铁状态与Thy1表达之间是否存在直接关系。铁螯合以剂量和时间依赖性方式显著降低PC12细胞中Thy1的表达。铁螯合时转铁蛋白受体表达增加,表明蛋白质合成的整体减少不能解释Thy1的变化。我们还检测了由缺铁(ID)饮食喂养的母鼠哺育的成年大鼠的脑匀浆,发现与对照大鼠相比,Thy1显著降低。最后,据报道,患有不安腿综合征的个体黑质中铁含量低于正常水平。因此,我们检测了临床诊断为原发性不安腿综合征(RLS)个体的该脑区,发现Thy1浓度不到对照组的一半。这些研究结果支持了Thy1与铁之间存在关系这一新概念,并指出了缺铁影响脑功能的新机制。它们还表明了缺铁损害RLS中多巴胺能传递的可能机制,为脑铁减少与RLS中对左旋多巴和铁补充治疗的反应性之间提供了潜在的重要联系。