Raghavendra Pongali B, Lee Eunhee, Parameswaran Narayanan
Department of Physiology and Division of Human Pathology, Michigan State University, 2201 Biomedical Physical Sciences building, East Lansing, MI, 48823, USA.
J Neuroimmune Pharmacol. 2014 Jun;9(3):277-84. doi: 10.1007/s11481-013-9516-y. Epub 2013 Nov 27.
Lithium (Li) continues to be a standard small compound used for the treatment of neurological disorders. Besides neuronal cells, Li is also known to affect immune cell function. In spite of its clinical use, potential mechanisms by which Li modulates immune cells, especially macrophages and its clinical relevance in bipolar patients are not well understood. Here, we provide an overview of the literature with regard to Li's effects on monocytes and macrophages. We have also included some of our results showing that Li differentially modulates chemokine gene expression in the absence and presence of Toll-like receptor-4 stimulation in a human macrophage model. Given that Li has a wide range of intracellular targets both in macrophages as well as in other cell types, more studies are needed to further understand the mechanistic basis of Li's effect in neurological and other inflammatory diseases. These studies could undoubtedly identify new therapeutic targets for treating such diseases.
锂(Li)仍然是用于治疗神经疾病的一种标准小分子化合物。除了神经元细胞外,锂还已知会影响免疫细胞功能。尽管锂已在临床中使用,但其调节免疫细胞(尤其是巨噬细胞)的潜在机制以及在双相情感障碍患者中的临床相关性仍未得到充分理解。在此,我们概述了关于锂对单核细胞和巨噬细胞影响的文献。我们还纳入了一些我们的研究结果,这些结果表明在人类巨噬细胞模型中,锂在有无Toll样受体4刺激的情况下对趋化因子基因表达有不同的调节作用。鉴于锂在巨噬细胞以及其他细胞类型中有广泛的细胞内靶点,需要更多研究来进一步了解锂在神经疾病和其他炎症性疾病中作用的机制基础。这些研究无疑能够确定治疗此类疾病的新治疗靶点。