Davis Terence, Rokicki Michal J, Bagley Mark C, Kipling David
Institute of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, CF14 4XN, UK.
Chem Cent J. 2013 Jan 29;7(1):18. doi: 10.1186/1752-153X-7-18.
Fibroblasts derived from the progeroid Werner syndrome (WS) show reduced replicative lifespan and a "stressed" morphology, both phenotypes being alleviated by using the p38 MAP kinase inhibitor SB203580. Because p38 is a major hub for the control of stress-signalling pathways we were interested in examining the possible role for downstream kinases in order to refine our understanding of the role of p38 signalling in regulation of WS cell growth. To this end we treated WS and normal fibroblasts with MK2 inhibitors to determine whether MK2 inhibition would affect either the growth or morphology of WS cells. The first inhibitor, 7,8-dihydroxy-2,4-diamino-3-cyanobenzopyranopyridine (inhibitor 2), resulted in inhibition of WS cell growth and had no effect on morphology, effects that occurred below the level needed to inhibit MK2 and thus suggestive of inhibitor toxicity. The second inhibitor, 2-(2-quinolin-3-ylpyridin-4-yl)-1,5,6,7-tetrahydro-4H-pyrrolo-[3,2-c]pyridin-4-one (CMPD16), resulted in a significant extension of WS fibroblast replicative capacity compared to normal cells. In addition, CMPD16 reverted the WS cellular morphology to that seen in normal dermal fibroblasts. These data suggest that MK2 activity plays a substantial role in proliferation control in WS cells. CMPD16 was not as effective in cellular lifespan extension as SB203580, however, suggesting that, although MK2 is a downstream kinase involved in cell cycle arrest, other p38 targets may play a role. Alternatively, as CMPD16 is toxic to cell growth at levels just above those that extend lifespan, it is possible that the therapeutic window is too small. However, as CMPD16 does show significant effects in WS fibroblasts, this acts as proof-of-principle for the efforts to design and synthesise improved MK2 inhibitors. As MK2 is involved in inflammatory processes and inflammation plays a major role in WS phenotypes, these data suggest MK2 as a potential therapeutic target for the treatment of Werner syndrome.
早老性沃纳综合征(WS)来源的成纤维细胞表现出复制寿命缩短和“应激”形态,使用p38丝裂原活化蛋白激酶抑制剂SB203580可缓解这两种表型。由于p38是应激信号通路控制的主要枢纽,我们有兴趣研究下游激酶的可能作用,以便更深入地了解p38信号在WS细胞生长调控中的作用。为此,我们用MK2抑制剂处理WS和正常成纤维细胞,以确定抑制MK2是否会影响WS细胞的生长或形态。第一种抑制剂,7,8 - 二羟基 - 2,4 - 二氨基 - 3 - 氰基苯并吡喃吡啶(抑制剂2),导致WS细胞生长受到抑制,且对形态无影响,这些作用发生在抑制MK2所需水平以下,因此提示抑制剂毒性。第二种抑制剂,2 - (2 - 喹啉 - 3 - 基吡啶 - 4 - 基) - 1,5,6,7 - 四氢 - 4H - 吡咯并[3,2 - c]吡啶 - 4 - 酮(CMPD16),与正常细胞相比,导致WS成纤维细胞的复制能力显著延长。此外,CMPD16使WS细胞形态恢复为正常真皮成纤维细胞的形态。这些数据表明MK2活性在WS细胞的增殖控制中起重要作用。然而,CMPD16在细胞寿命延长方面不如SB203580有效,这表明,尽管MK2是参与细胞周期停滞的下游激酶,但其他p38靶点可能也发挥作用。或者,由于CMPD16在略高于延长寿命的水平时对细胞生长有毒性,有可能治疗窗口太小。然而,由于CMPD16确实在WS成纤维细胞中显示出显著作用,这为设计和合成改进的MK2抑制剂的努力提供了原理证明。由于MK2参与炎症过程且炎症在WS表型中起主要作用,这些数据表明MK2作为治疗沃纳综合征的潜在治疗靶点。