Laboratory of Nephrology and Vascular Pathology, Instituto de Investigación Sanitaria-Fundación Jiménez Díaz, Madrid, Spain.
PLoS One. 2013;8(1):e51992. doi: 10.1371/journal.pone.0051992. Epub 2013 Jan 2.
The polyglutamic acid/peptoid 1 (QM56) nanoconjugate inhibits apoptosis by interfering with Apaf-1 binding to procaspase-9. We now describe anti-inflammatory properties of QM56 in mouse kidney and renal cell models.In cultured murine tubular cells, QM56 inhibited the inflammatory response to Tweak, a non-apoptotic stimulus. Tweak induced MCP-1 and Rantes synthesis through JAK2 kinase and NF-κB activation. Similar to JAK2 kinase inhibitors, QM56 inhibited Tweak-induced NF-κB transcriptional activity and chemokine expression, despite failing to inhibit NF-κB-p65 nuclear translocation and NF-κB DNA binding. QM56 prevented JAK2 activation and NF-κB-p65(Ser536) phosphorylation. The anti-inflammatory effect and JAK2 inhibition by QM56 were observed in Apaf-1(-/-) cells. In murine acute kidney injury, QM56 decreased tubular cell apoptosis and kidney inflammation as measured by down-modulations of MCP-1 and Rantes mRNA expression, immune cell infiltration and activation of the JAK2-dependent inflammatory pathway.In conclusion, QM56 has an anti-inflammatory activity which is independent from its role as inhibitor of Apaf-1 and apoptosis and may have potential therapeutic relevance.
聚谷氨酸/肽 1(QM56)纳米缀合物通过干扰 Apaf-1 与 procaspase-9 的结合来抑制细胞凋亡。我们现在描述了 QM56 在小鼠肾脏和肾细胞模型中的抗炎特性。在培养的鼠肾小管细胞中,QM56 抑制了 Tweak(一种非凋亡刺激物)引起的炎症反应。Tweak 通过 JAK2 激酶和 NF-κB 激活诱导 MCP-1 和 Rantes 的合成。与 JAK2 激酶抑制剂相似,QM56 抑制了 Tweak 诱导的 NF-κB 转录活性和趋化因子表达,尽管未能抑制 NF-κB-p65 核转位和 NF-κB DNA 结合。QM56 可预防 JAK2 激活和 NF-κB-p65(Ser536)磷酸化。在 Apaf-1(-/-)细胞中观察到 QM56 的抗炎作用和 JAK2 抑制作用。在小鼠急性肾损伤中,QM56 通过下调 MCP-1 和 Rantes mRNA 表达、免疫细胞浸润和激活 JAK2 依赖性炎症途径,减少肾小管细胞凋亡和肾脏炎症。总之,QM56 具有抗炎活性,与它作为 Apaf-1 和细胞凋亡抑制剂的作用无关,可能具有潜在的治疗相关性。