艾灸通过sirt5介导的翻译后修饰和巨噬细胞极化缓解炎症。

IF 4.5 2区 医学 Q2 CELL BIOLOGY
Chuan-Yi Zuo, Cheng-Shun Zhang, Han-Xiao Zhang, Chun-Yan Gou, Hong Lei, Feng-Wei Tian, Zhu-Xing Wang, Hai-Yan Yin, Shu-Guang Yu
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引用次数: 0

摘要

巨噬细胞极化受Sirtuin5 (SIRT5)的影响,SIRT5对调节抗炎过程至关重要。艾灸通过改变巨噬细胞M1向M2转移的指标琥珀酸/α-酮戊二酸(α-KG)比值发挥抗炎作用。谷氨酸脱氢酶1 (Glutamate dehydrogenase 1, GLUD1)是参与α-KG生成的关键酶,可被SIRT5去琥珀酰化。目前,艾灸对炎性疾病中SIRT5-GLUD1-α- kg介导的巨噬细胞极化的潜在影响尚不清楚。C57BL/6 J和Sirt5基因敲除小鼠作为完全Freund's佐剂(CFA)诱导的佐剂性关节炎模型。给予MC3482艾灸和穴位注射。采用爪容量测定和ELISA法定量观察炎症效应、琥珀酸盐和α-KG的表达。采用流式细胞术(FCM)和免疫荧光法检测巨噬细胞M1样和m2样的表达。进行LC-MS/MS-based蛋白质组学分析,鉴定出GLUD1与SIRT5相关的去琥珀酰化蛋白。Western blotting和免疫沉淀(IP)检测SIRT5、GLUD1和琥珀酰化GLUD1的表达。在CFA模型中,艾灸和sirt5介导的去琥珀酰化抑制剂MC3482通过增加M2巨噬细胞数量和减少M1巨噬细胞数量来减轻炎症。其潜在机制可能与艾灸和SIRT5抑制作用有关,抑制了CFA组琥珀酸盐和α-KG水平,导致治疗后琥珀酸盐低,α-KG高,GLUD1琥珀酰化升高。这些发现提示,艾灸的抗炎作用与sirt5介导的翻译后修饰后巨噬细胞转化的影响有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Moxibustion Alleviates Inflammation via SIRT5-mediated Post-translational Modification and Macrophage Polarization.

Macrophage polarisation is influenced by Sirtuin5 (SIRT5), which is crucial for regulating anti-inflammatory processes. Moxibustion, a traditional Chinese medicine therapy, exerts anti-inflammatory effects by altering the succinate/α-ketoglutarate (α-KG) ratio, an indicator of the M1 to M2 macrophage shift. Glutamate dehydrogenase 1 (GLUD1), a key enzyme involved in α-KG production, is desuccinylated by SIRT5. Currently, the potential influence of moxibustion on SIRT5-GLUD1-α-KG-mediated macrophage polarization in inflammatory diseases remains unexplored. C57BL/6 J and Sirt5 knockout mice were used as complete Freund's adjuvant (CFA)-induced adjuvant arthritis models. Moxibustion and acupoint injections of MC3482 were administered. Paw capacity asssays and ELISA were performed to quantify inflammatory effects and the expression of succinate, and α-KG expressions. Flow cytometry (FCM) and immunofluorescence were used to assesss the expression of M1- and M2-like macrophages. LC-MS/MS-based proteomic analysis was performed, and GLUD1 was identified desuccinylated protein associated with SIRT5. Western blotting and immunoprecipitation (IP) were used to detect SIRT5, GLUD1, and succinylated GLUD1expressions. Moxibustion and the SIRT5-mediated desuccinylation inhibitor MC3482 decreased inflammation by increasing the number of M2 macrophages and reducing the number of M1 macrophage in the CFA model. The potential mechanism may be related to the effects of moxibustion and SIRT5 inhibition, which inverted succinate and α-KG levels in the CFA group, resulting in low succinate, high α-KG, and increased GLUD1 succinylation after treatment. These findings suggest that the anti-inflammatory effects moxibustion are related to the impact of macrophage conversion after SIRT5-mediated post-translational modification.

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来源期刊
Inflammation
Inflammation 医学-免疫学
CiteScore
9.70
自引率
0.00%
发文量
168
审稿时长
3.0 months
期刊介绍: Inflammation publishes the latest international advances in experimental and clinical research on the physiology, biochemistry, cell biology, and pharmacology of inflammation. Contributions include full-length scientific reports, short definitive articles, and papers from meetings and symposia proceedings. The journal''s coverage includes acute and chronic inflammation; mediators of inflammation; mechanisms of tissue injury and cytotoxicity; pharmacology of inflammation; and clinical studies of inflammation and its modification.
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