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硫化氢诱导 GAPDH 巯基化破坏 CCAR2-SIRT1 相互作用以启动自噬。

Hydrogen sulfide-induced GAPDH sulfhydration disrupts the CCAR2-SIRT1 interaction to initiate autophagy.

机构信息

Council of Scientific and Industrial Research, Institute of Microbial Technology, Chandigarh, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, India.

出版信息

Autophagy. 2021 Nov;17(11):3511-3529. doi: 10.1080/15548627.2021.1876342. Epub 2021 Jan 30.

Abstract

The deacetylase SIRT1 (sirtuin 1) has emerged as a major regulator of nucleocytoplasmic distribution of macroautophagy/autophagy marker MAP1LC3/LC3 (microtubule-associated protein 1 light chain 3). Activation of SIRT1 leads to the deacetylation of LC3 and its translocation from the nucleus into the cytoplasm leading to an increase in the autophagy flux. Notably, hydrogen sulfide (HS) is a cytoprotective gasotransmitter known to activate SIRT1 and autophagy; however, the underlying mechanism for both remains unknown. Herein, we demonstrate that HS sulfhydrates the active site cysteine of the glycolytic enzyme GAPDH (glyceraldehyde-3-phosphate dehydrogenase). Sulfhydration of GAPDH leads to its redistribution into the nucleus. Importantly, nuclear localization of GAPDH is critical for HS-mediated activation of autophagy as HS does not induce autophagy in cells with GAPDH ablation or cells overexpressing a GAPDH mutant lacking the active site cysteine. Importantly, we observed that nuclear GAPDH interacts with CCAR2/DBC1 (cell cycle activator a nd apoptosis regulator 2) inside the nucleus. CCAR2 interacts with the deacetylase SIRT1 to inhibit its activity. Interaction of GAPDH with CCAR2 disrupts the inhibitory effect of CCAR2 on SIRT1. Activated SIRT1 then deacetylates MAP1LC3B/LC3B (microtubule-associated protein 1 light chain 3 beta) to induce its translocation into the cytoplasm and activate autophagy. Additionally, we demonstrate this pathway's physiological role in autophagy-mediated trafficking of into lysosomes to restrict intracellular mycobacteria growth. We think that the pathway described here could be involved in HS-mediated clearance of intracellular pathogens and other health benefits.: ATG5: autophagy related 5; ATG7: autophagy related 7; BECN1: beclin 1, autophagy related; CCAR2/DBC1: cell cycle activator and apoptosis regulator 2; CFU: colony-forming units; DLG4/PSD95: discs large MAGUK scaffold protein 4; EX-527: 6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide; GAPDH: glyceraldehyde-3-phosphate dehydrogenase; HS: hydrogen sulfide; HEK: human embryonic kidney cells; MAP1LC3B/LC3B: microtubule-associated protein 1 light chain 3 beta; MEF: mouse embryonic fibroblast; ; MTOR: mechanistic target of rapamycin kinase; MOI: multiplicity of infection; NO: nitric oxide; PI3K: phosphatidylinositol-4,5-bisphosphate 3-kinase; PLA: proximity ligation assay; PRKAA: protein kinase, AMP-activated, alpha catalytic subunit; SIAH1: siah E3 ubiquitin protein ligase 1A; SIRT1: sirtuin 1; TB: tuberculosis; TP53INP2/DOR: transformation related protein 53 inducible nuclear protein 2; TRP53/TP53: transformation related protein 53.

摘要

去乙酰化酶 SIRT1(沉默调节蛋白 1)已成为调控大自噬/自噬标志物 MAP1LC3/LC3(微管相关蛋白 1 轻链 3)核质分布的主要调节因子。SIRT1 的激活导致 LC3 的去乙酰化及其从核内易位到细胞质内,从而增加自噬通量。值得注意的是,硫化氢(HS)是一种已知能激活 SIRT1 和自噬的细胞保护气体递质;然而,其潜在的机制仍不清楚。在此,我们证明 HS 使糖酵解酶 GAPDH(甘油醛-3-磷酸脱氢酶)的活性半胱氨酸发生硫氢化作用。GAPDH 的硫氢化作用导致其重新分布到核内。重要的是,GAPDH 的核定位对于 HS 介导的自噬激活至关重要,因为 HS 不会诱导 GAPDH 缺失的细胞或过表达缺乏活性半胱氨酸的 GAPDH 突变体的细胞发生自噬。重要的是,我们观察到核内的 GAPDH 与核内的 CCAR2/DBC1(细胞周期激活因子和凋亡调节剂 2)相互作用。CCAR2 与去乙酰化酶 SIRT1 相互作用以抑制其活性。GAPDH 与 CCAR2 的相互作用破坏了 CCAR2 对 SIRT1 的抑制作用。激活的 SIRT1 然后去乙酰化 MAP1LC3B/LC3B(微管相关蛋白 1 轻链 3β),使其易位到细胞质内,并激活自噬。此外,我们证明了该途径在自噬介导的进入溶酶体以限制细胞内分枝杆菌生长中的生理作用。我们认为,这里描述的途径可能参与 HS 介导的细胞内病原体清除和其他健康益处。:ATG5:自噬相关蛋白 5;ATG7:自噬相关蛋白 7;BECN1:自噬相关蛋白 Beclin 1;CCAR2/DBC1:细胞周期激活因子和凋亡调节剂 2;CFU:集落形成单位;DLG4/PSD95:Discs large MAGUK 支架蛋白 4;EX-527:6-氯-2,3,4,9-四氢-1H-咔唑-1-羧酰胺;GAPDH:甘油醛-3-磷酸脱氢酶;HS:硫化氢;HEK:人胚肾细胞;;MTOR:雷帕霉素靶蛋白激酶;MOI:感染复数;NO:一氧化氮;PI3K:磷脂酰肌醇-4,5-二磷酸 3-激酶;PLA:邻近连接分析;PRKAA:蛋白激酶 AMP 激活型,α催化亚基;SIAH1:siah E3 泛素蛋白连接酶 1A;SIRT1:沉默调节蛋白 1;TB:结核病;TP53INP2/DOR:转化相关蛋白 53 诱导核蛋白 2;TRP53/TP53:转化相关蛋白 53。

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