Cheng Peng, Xie Jianwei, Liu Zhiyong, Wang Jian
Department of Neurology, Second Naval Hospital of Southern Theater Command (425th Hospital of the People's Liberation Army), Sanya, 572000, China.
Institute of Neurosciences, Fourth Military Medical University, Xi'an, 710032, China.
Cell Biosci. 2021 Mar 26;11(1):61. doi: 10.1186/s13578-021-00576-7.
Macrophage M1 polarization mediates inflammatory responses and tissue damage. Recently, aldose reductase (AR) has been shown to play a critical role in M1 polarization in macrophages. However, the underlying mechanisms are unknown. Here, we demonstrated, for the first time, that AR deficiency repressed the induction of inducible nitric oxide synthase in lipopolysaccharide (LPS)-stimulated macrophages via activation of autophagy. This suppression was related to a defect in the inhibitor of nuclear factor κB (NF-κB) kinase (IKK) complex in the classical NF-κB pathway. However, the mRNA levels of IKKβ and IKKγ were not reduced in LPS-treated AR knockout (KO) macrophages, indicating that their proteins were downregulated at the post-transcriptional level. We discovered that LPS stimuli induced the recruitment of more beclin1 and increased autophagosome formation in AR-deficient macrophages. Blocking autophagy through 3-methyladenine and ammonium chloride treatment restored IKKβ and IKKγ protein levels and increased nitric oxide synthase production in LPS-stimulated AR-deficient macrophages. More assembled IKKβ and IKKγ underwent ubiquitination and recruited the autophagic adaptor p62 in LPS-induced AR KO macrophages, promoting their delivery to autophagosomes and lysosomes. Collectively, these findings suggest that AR deficiency is involved in the regulation of NF-κB signaling, and extends the role of selective autophagy in fine-tuned M1 macrophage polarization.
巨噬细胞M1极化介导炎症反应和组织损伤。最近,已证明醛糖还原酶(AR)在巨噬细胞的M1极化中起关键作用。然而,其潜在机制尚不清楚。在此,我们首次证明,AR缺陷通过激活自噬抑制脂多糖(LPS)刺激的巨噬细胞中诱导型一氧化氮合酶的诱导。这种抑制与经典核因子κB(NF-κB)途径中核因子κB(NF-κB)激酶(IKK)复合物抑制剂的缺陷有关。然而,在LPS处理的AR基因敲除(KO)巨噬细胞中,IKKβ和IKKγ的mRNA水平并未降低,表明它们的蛋白质在转录后水平下调。我们发现,LPS刺激在AR缺陷的巨噬细胞中诱导更多的beclin1募集并增加自噬体形成。通过3-甲基腺嘌呤和氯化铵处理阻断自噬可恢复LPS刺激的AR缺陷巨噬细胞中IKKβ和IKKγ蛋白水平,并增加一氧化氮合酶的产生。在LPS诱导的AR KO巨噬细胞中,更多组装的IKKβ和IKKγ发生泛素化并募集自噬衔接蛋白p62,促进它们被递送至自噬体和溶酶体。总的来说,这些发现表明AR缺陷参与NF-κB信号传导的调节,并扩展了选择性自噬在微调M1巨噬细胞极化中的作用。