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腺苷酸激酶 4 促进巨噬细胞中炎症基因表达 Hif1α 和 AMPK。

Adenylate Kinase 4 Promotes Inflammatory Gene Expression Hif1α and AMPK in Macrophages.

机构信息

Graduate Institute of Immunology, National Taiwan University College of Medicine, Taipei, Taiwan.

Bioinformatics and Biostatistics Core, Center of Genomic and Precision Medicine, National Taiwan University, Taipei, Taiwan.

出版信息

Front Immunol. 2021 Mar 15;12:630318. doi: 10.3389/fimmu.2021.630318. eCollection 2021.

Abstract

Macrophages comprise the front line of defense against various pathogens. Classically activated macrophages (M1), induced by IFN-γ and LPS, highly express inflammatory cytokines and contribute to inflammatory processes. By contrast, alternatively activated macrophages (M2) are induced by IL-4 and IL-13, produce IL-10, and display anti-inflammatory activity. Adenylate kinase 4 (Ak4), an enzyme that transfers phosphate group among ATP/GTP, AMP, and ADP, is a key modulator of ATP and maintains the homeostasis of cellular nucleotides which is essential for cell functions. However, its role in regulating the function of macrophages is not fully understood. Here we report that Ak4 expression is induced in M1 but not M2 macrophages. Suppressing the expression of Ak4 in M1 macrophages with shRNA or siRNA enhances ATP production and decreases ROS production, bactericidal ability and glycolysis in M1 cells. Moreover, Ak4 regulates the expression of inflammation genes, including , and , in M1 macrophages. We further demonstrate that Ak4 inhibits the activation of AMPK and forms a positive feedback loop with Hif1α to promote the expression of inflammation-related genes in M1 cells. Furthermore, RNA-seq analysis demonstrates that Ak4 also regulates other biological processes in addition to the expression of inflammation-related genes in M1 cells. Interestingly, Ak4 does not regulate M1/M2 polarization. Taken together, our study uncovers a potential mechanism linking energy consumption and inflammation in macrophages.

摘要

巨噬细胞构成了抵御各种病原体的第一道防线。经典激活的巨噬细胞(M1),由 IFN-γ 和 LPS 诱导,高度表达炎症细胞因子,有助于炎症过程。相比之下,替代激活的巨噬细胞(M2)由 IL-4 和 IL-13 诱导,产生 IL-10,并表现出抗炎活性。腺苷酸激酶 4(Ak4)是一种在 ATP/GTP、AMP 和 ADP 之间转移磷酸基团的酶,是 ATP 的关键调节剂,维持细胞核苷酸的内稳态,这对于细胞功能至关重要。然而,它在调节巨噬细胞功能中的作用尚不完全清楚。在这里,我们报告 Ak4 在 M1 巨噬细胞中被诱导表达,但在 M2 巨噬细胞中不被诱导表达。用 shRNA 或 siRNA 抑制 M1 巨噬细胞中 Ak4 的表达可增强 ATP 产生,减少 ROS 产生、M1 细胞的杀菌能力和糖酵解。此外,Ak4 调节 M1 巨噬细胞中炎症基因的表达,包括 、 和 。我们进一步证明,Ak4 抑制 AMPK 的激活,并与 Hif1α 形成正反馈回路,以促进 M1 细胞中炎症相关基因的表达。此外,RNA-seq 分析表明,Ak4 除了调节 M1 细胞中炎症相关基因的表达外,还调节其他生物学过程。有趣的是,Ak4 不调节 M1/M2 极化。总之,我们的研究揭示了一种潜在的机制,将巨噬细胞中的能量消耗与炎症联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b66/8005550/8661c877ae11/fimmu-12-630318-g0001.jpg

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