...
首页> 外文期刊>The Journal of Pharmacology and Experimental Therapeutics: Official Publication of the American Society for Pharmacology and Experimental Therapeutics >The Antipsoriatic Agent Monomethylfumarate Has Antiproliferative, Prodifferentiative, and Anti-Inflammatory Effects on Keratinocytes
【24h】

The Antipsoriatic Agent Monomethylfumarate Has Antiproliferative, Prodifferentiative, and Anti-Inflammatory Effects on Keratinocytes

机译:抗牛皮癣药物富马酸单甲酯对角质形成细胞具有抗增殖,促增殖和抗炎作用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Monomethylfumarate (MMF) is thought to be the bioactive ingredient of the drug Fumaderm (Biogen Idec, Cambridge, MA), licensed in Germany since 1994 for the treatment of moderate-to-severe psoriasis. Psoriasis is a common inflammatory hyper-proliferative skin disorder that involves cross-talk between different cell types, including immune cells and keratinocytes. Psoriatic lesions are characterized by hyperproliferation, aberrant differentiation, and inflammation, with the psoriatic cytokine network maintained by communication between immune cells and keratinocytes. Recently, there is increasing evidence regarding the pivotal role of keratinocytes in mediating the disease process, and these cells can be regarded as safe therapeutic targets. From the data available on human subjects treated with Fumaderm, MMF is an effective antipsoriatic agent with known effects on immune cells. However, little is known about its direct effects on keratinocytes. We hypothesized that MMF has direct antiproliferative, prodifferentiative, and anti-inflammatory effects on keratinocytes. Indeed, MMF dose-dependently inhibited [H-3]thymidine incorporation into DNA, indicating a direct antiproliferative action on keratinocytes. MMF significantly increased the protein level of keratin 10, the early keratinocyte differentiation marker, and the activity of transglutaminase, a late differentiation marker. These results are consistent with an ability of MMF to promote keratinocyte differentiation and inhibit proliferation, thereby improving psoriatic lesions. In 12-O-tetradecanoylphorbol-13- acetate (TPA)-induced keratinocytes, MMF significantly inhibited the expression of the proinflammatory cytokines, tumor necrosis factor-alpha (TNF alpha), interleukin-6, and interleukin-1 alpha as well as the production of TNF alpha. Our results support the notion that MMF has direct antiproliferative, prodifferentiative, and anti-inflammatory effects on keratinocytes, highlighting its potential use as a multifactorial antipsoriatic agent.
机译:富马酸单甲酯(MMF)被认为是Fumaderm药物(Biogen Idec,Cambridge,MA)的生物活性成分,该药物于1994年在德国获得许可,用于治疗中度至重度牛皮癣。牛皮癣是一种常见的炎症性过度增生性皮肤病,涉及不同细胞类型(包括免疫细胞和角质形成细胞)之间的串扰。银屑病病变的特征在于过度增殖,异常分化和炎症,并且通过免疫细胞和角质形成细胞之间的通信来维持银屑病细胞因子网络。最近,关于角质形成细胞在介导疾病过程中的关键作用的证据越来越多,这些细胞可被视为安全的治疗靶标。从有关用Fumaderm治疗的人类受试者的可用数据来看,MMF是一种有效的抗银屑病药物,对免疫细胞有已知作用。然而,关于其对角质形成细胞的直接作用知之甚少。我们假设MMF对角质形成细胞具有直接的抗增殖,增生和抗炎作用。实际上,MMF剂量依赖性地抑制[H-3]胸苷掺入DNA中,表明对角质形成细胞具有直接的抗增殖作用。 MMF显着增加了早期角质形成细胞分化标记角蛋白10的蛋白质水平,以及晚期分化标记物转谷氨酰胺酶的活性。这些结果与MMF促进角质形成细胞分化和抑制增殖从而改善牛皮癣损伤的能力一致。在12-O-十四烷酰phorbol-13-乙酸盐(TPA)诱导的角质形成细胞中,MMF显着抑制促炎细胞因子,肿瘤坏死因子-α(TNF alpha),白细胞介素6和白细胞介素-1α的表达。 TNFα的产生。我们的结果支持以下观点:MMF对角质形成细胞具有直接的抗增殖,增生和抗炎作用,突显了其作为多因素抗银屑病药物的潜在用途。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号