Department of Neurology, University of Szeged, Semmelweis u. 6, H-6725 Szeged, Hungary.
Neurosci Lett. 2013 Oct 25;554:131-4. doi: 10.1016/j.neulet.2013.08.069. Epub 2013 Sep 8.
Peroxisome proliferator-activated receptor gamma (PPARγ), a ligand-activated transcriptional factor involved in the regulation of glucose and lipid metabolism, has gained interest as a potential therapeutic target in multiple sclerosis (MS) due to its potent immunoregulatory properties and the therapeutic efficacy of its ligands in experimental autoimmune encephalitis (EAE). Elevated expression of PPARγ has been observed in the spinal cord of EAE mice and in an in vitro model of antigen-induced demyelination; however, no reports have yet been available on the PPARγ status in the central nervous system of human individuals with MS. Aiming to identify a possible alteration, the present study assessed the levels of PPARγ protein in the cerebrospinal fluid (CSF) of MS patients via ELISA technique. We report a pronounced elevation in the CSF levels of PPARγ in MS patients (n=35) compared to non-inflammatory controls (n=22). This elevation was independent of blood-CSF barrier integrity, but correlated with CSF white blood cell count and IgG index, associating the observed elevation with neuroinflammation. Controlling for potential confounders, the CSF levels of PPARγ further displayed a moderate but significant association with clinical severity. Corroborating with prior experimental findings, these results may contribute to our understanding about the role of PPARγ in MS, and may implicate this protein as a potential CSF biomarker of the disease.
过氧化物酶体增殖物激活受体 γ(PPARγ)是一种配体激活的转录因子,参与葡萄糖和脂质代谢的调节,由于其强大的免疫调节特性及其配体在实验性自身免疫性脑脊髓炎(EAE)中的治疗功效,它已成为多发性硬化症(MS)的潜在治疗靶点而受到关注。在 EAE 小鼠的脊髓和抗原诱导的脱髓鞘体外模型中观察到 PPARγ 的表达升高;然而,目前尚无关于 MS 患者中枢神经系统中 PPARγ 状态的报告。为了确定可能的改变,本研究通过 ELISA 技术评估了 MS 患者脑脊液(CSF)中 PPARγ 蛋白的水平。我们报告称,与非炎症性对照组(n=22)相比,MS 患者(n=35)CSF 中的 PPARγ 水平明显升高。这种升高与血脑屏障完整性无关,但与 CSF 白细胞计数和 IgG 指数相关,表明观察到的升高与神经炎症有关。控制潜在的混杂因素后,CSF 中 PPARγ 的水平与临床严重程度呈中度但显著相关。与之前的实验结果相吻合,这些结果可能有助于我们了解 PPARγ 在 MS 中的作用,并可能暗示该蛋白作为该疾病潜在的 CSF 生物标志物。