Wang Pei-Hua, Wang Yan, Guo Yan-Yan, Ma Zi-Hui, Wu Changxin, Xing Li
Institutes of Biomedical Sciences, Shanxi University, 92 Wucheng Road, Taiyuan 030006, Shanxi Province, China.
Institutes of Biomedical Sciences, Shanxi University, 92 Wucheng Road, Taiyuan 030006, Shanxi Province, China; Shanxi Provincial Key Laboratory of Medical Molecular Cell Biology, Shanxi University, 92 Wucheng Road, Taiyuan 030006, China.
Int Immunopharmacol. 2024 Dec 25;143(Pt 3):113502. doi: 10.1016/j.intimp.2024.113502. Epub 2024 Nov 2.
Ibuprofen, a non-steroidal drug, is well known for its anti-inflammatory activity. The effects of ibuprofen on the polarization of macrophages are still not clear. Herein, we used THP-1 monocyte-derived macrophages to find that ibuprofen has inhibitory effects on the polarization of both classically activated M1 macrophages and alternatively activated M2 macrophages by downregulating NF-κB and JAK/STAT signaling pathways. During M1 or M2 polarization, ibuprofen also downregulated the expression of poly (ADP-ribose) polymerase 1 (PARP1). Furthermore, knockdown of PARP1 by either small interfering RNA or PARP1 inhibitor PJ34 can exert inhibitory effects on the polarization of M1 and M2, and alter the immune response of macrophages to the infection of Mycobacterium tuberculosis H37Ra. The results demonstrate that PARP1 plays a regulatory role in the ibuprofen-modulated polarization of macrophage, revealing the interplay between the DNA repair response process and macrophage polarization.
布洛芬是一种非甾体类药物,以其抗炎活性而闻名。布洛芬对巨噬细胞极化的影响仍不清楚。在此,我们使用THP-1单核细胞衍生的巨噬细胞发现,布洛芬通过下调NF-κB和JAK/STAT信号通路,对经典活化的M1巨噬细胞和交替活化的M2巨噬细胞的极化均具有抑制作用。在M1或M2极化过程中,布洛芬还下调了聚(ADP-核糖)聚合酶1(PARP1)的表达。此外,通过小干扰RNA或PARP1抑制剂PJ34敲低PARP1可对M1和M2的极化产生抑制作用,并改变巨噬细胞对结核分枝杆菌H37Ra感染的免疫反应。结果表明,PARP1在布洛芬调节的巨噬细胞极化中起调节作用,揭示了DNA修复反应过程与巨噬细胞极化之间的相互作用。