Center for Kidney Disease, 2nd Affiliated Hospital, Nanjing Medical University, Nanjing, Jiangsu Province, China.
PLoS One. 2012;7(6):e39738. doi: 10.1371/journal.pone.0039738. Epub 2012 Jun 25.
Inflammation is a pathologic feature of hyperuricemia in clinical settings. However, the underlying mechanism remains unknown. Here, infiltration of T cells and macrophages were significantly increased in hyperuricemia mice kidneys. This infiltration of inflammatory cells was accompanied by an up-regulation of TNF-α, MCP-1 and RANTES expression. Further, infiltration was largely located in tubular interstitial spaces, suggesting a role for tubular cells in hyperuricemia-induced inflammation. In cultured tubular epithelial cells (NRK-52E), uric acid, probably transported via urate transporter, induced TNF-α, MCP-1 and RANTES mRNA as well as RANTES protein expression. Culture media of NRK-52E cells incubated with uric acid showed a chemo-attractive ability to recruit macrophage. Moreover uric acid activated NF-κB signaling. The uric acid-induced up-regulation of RANTES was blocked by SN 50, a specific NF-κB inhibitor. Activation of NF-κB signaling was also observed in tubule of hyperuricemia mice. These results suggest that uric acid induces renal inflammation via activation of NF-κB signaling.
在临床环境中,炎症是高尿酸血症的病理特征。然而,其潜在机制尚不清楚。在这里,高尿酸血症小鼠肾脏中 T 细胞和巨噬细胞浸润明显增加。这种炎症细胞的浸润伴随着 TNF-α、MCP-1 和 RANTES 表达的上调。此外,浸润主要位于肾小管间质空间,提示肾小管细胞在高尿酸血症诱导的炎症中起作用。在培养的肾小管上皮细胞(NRK-52E)中,尿酸可能通过尿酸转运蛋白转运,诱导 TNF-α、MCP-1 和 RANTES mRNA 以及 RANTES 蛋白表达。与尿酸孵育的 NRK-52E 细胞的培养基显示出招募巨噬细胞的趋化能力。此外,尿酸激活了 NF-κB 信号通路。NF-κB 抑制剂 SN 50 阻断了尿酸诱导的 RANTES 上调。高尿酸血症小鼠肾小管中也观察到 NF-κB 信号的激活。这些结果表明,尿酸通过激活 NF-κB 信号通路诱导肾脏炎症。