Pandey Ghanshyam N
Department of Psychiatry, University of Illinois at Chicago, Chicago, IL, USA.
Mod Trends Pharmacopsychiatry. 2017;31:79-95. doi: 10.1159/000470809. Epub 2017 Jul 24.
Several studies suggest that major depressive disorder (MDD) and bipolar disorder (BPD) are neuroprogressive illnesses. Besides clinical features, neurobiological mechanisms have been suggested to contribute to the neuroprogression of mood disorders. Biological factors that have been shown to contribute significantly toward the neuroprogressive course of these disorders are inflammatory markers, such as cytokines. Cytokines have been extensively investigated, primarily in the serum of MDD and BPD patients, and these studies show cytokine abnormalities in both adolescent and adult patients with mood disorders. However, cytokine abnormalities in the brain may also contribute toward neuroprogression, but brain cytokines have not been adequately investigated. To examine the role of cytokines in neuroprogression, we have studied the markers of adaptive and innate immunity in postmortem brain obtained from teenage and adult suicide victims and gene expression of cytokines and their membrane-bound receptors in lymphocytes of MDD and BPD patients. Cytokines and Toll-like receptors (TLRs) were studied in 24 teenage suicide victims and 24 normal control (NC) subjects, and also in 22 adult depressed suicide victims and 20 adult NC subjects. We found that the protein and mRNA expression of the proinflammatory cytokines tumor necrosis factor (TNF)-α, interleukin (IL)-1β, and IL-6 were significantly higher in the prefrontal cortex (PFC). We also found that the protein and mRNA expression of TLRs, which are major mediators of innate immunity, is increased in the PFC of adult depressed suicide victims and NC subjects. In patients, mRNA and protein expression of TNF-α, IL-1β, and IL-6 was significantly increased in both MDD and BPD patients. Similarly, mRNA expression of some specific membrane-bound receptors, such as IL1R1, TNFR1, IL1RA, were significantly increased in lymphocytes of MDD and BPD patients. These studies indicate the existence of abnormal cytokines and TLRs in the brain of teenage and adult suicide victims. Future studies, including both teenage and adult postmortem samples, will be needed to further clarify the role of cytokines and TLRs in neuroprogression.
多项研究表明,重度抑郁症(MDD)和双相情感障碍(BPD)是神经退行性疾病。除临床特征外,神经生物学机制也被认为与情绪障碍的神经进展有关。已证明对这些疾病的神经进展有显著影响的生物学因素是炎症标志物,如细胞因子。细胞因子已得到广泛研究,主要是在MDD和BPD患者的血清中,这些研究表明,青少年和成年情绪障碍患者均存在细胞因子异常。然而,脑内细胞因子异常也可能导致神经进展,但脑内细胞因子尚未得到充分研究。为了研究细胞因子在神经进展中的作用,我们研究了青少年和成年自杀受害者死后大脑中适应性免疫和固有免疫的标志物,以及MDD和BPD患者淋巴细胞中细胞因子及其膜结合受体的基因表达。对24名青少年自杀受害者和24名正常对照(NC)受试者,以及22名成年抑郁自杀受害者和20名成年NC受试者进行了细胞因子和Toll样受体(TLR)研究。我们发现,前额叶皮质(PFC)中促炎细胞因子肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和IL-6的蛋白质和mRNA表达显著升高。我们还发现,作为固有免疫主要介质的TLR的蛋白质和mRNA表达在成年抑郁自杀受害者和NC受试者的PFC中增加。在患者中,MDD和BPD患者的TNF-α、IL-1β和IL-6的mRNA和蛋白质表达均显著增加。同样,MDD和BPD患者淋巴细胞中一些特定膜结合受体如IL1R1、TNFR1、IL1RA的mRNA表达也显著增加。这些研究表明,青少年和成年自杀受害者大脑中存在异常的细胞因子和TLR。未来的研究,包括青少年和成年尸检样本,将需要进一步阐明细胞因子和TLR在神经进展中的作用。