Gamma-aminobutyric acid type A receptor alpha 4 coordinates autophagy, inflammation, and immunometabolism to promote innate immune activation.

Autophagy reports Pub Date : 2023-03-01 eCollection Date: 2023-01-01 DOI:10.1080/27694127.2023.2181915
Jin Kyung Kim, Prashanta Silwal, Young Jae Kim, Sang Min Jeon, In Soo Kim, June-Young Lee, Jun Young Heo, Sang-Hee Lee, Jin-Woo Bae, Jin-Man Kim, Jin Bong Park, Eun-Kyeong Jo
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引用次数: 0

Abstract

Gamma-aminobutyric acid type A receptor (GABAAR), the ionotropic receptor of GABA, is expressed in macrophages and in the nervous system; however, its role in innate immunity is unknown. Herein, we identified myeloid GABAAR subunit α4 (Gabra4) as a critical regulator of autophagy and a promoter of host innate defense during infection and inflammation. Myeloid Gabra4 deficiency led to defective mycobacterial clearance during infection and increased susceptibility to septic shock. Gabra4 deletion exaggerated inflammatory responses and suppressed the activation of autophagy in macrophages upon infectious and inflammatory stimuli. Mechanistically, Gabra4-mediated signaling led to upregulation of autophagy in macrophages via intracellular calcium release and AMP-activated protein kinase (AMPK) signaling activation, which was required for linking autophagy and antimicrobial responses. Additionally, Gabra4 was required to generate mitochondrial reactive oxygen species, thereby triggering autophagy and antimicrobial responses to mycobacteria. Metabolomics analysis showed that Gabra4 was critical for glucose metabolism and aerobic glycolysis in macrophages. Our findings demonstrate that myeloid Gabra4 coordinates autophagy, inflammation, and immunometabolism to promote innate host defense against pathogenic and dangerous stimuli. Abbreviation AM: Alveolar macrophage; AMPK: AMP-activated protein kinase; ASC: Apoptosis-associated speck-like protein containing a CARD; ATP: Adenosine 5'-triphosphate; BAL: Bronchoalveolar lavage; BCG: Mycobacterium bovis Bacillus Calmette-Guérin; BMDM: Bone marrow-derived macrophage; CCL: CC motif chemokine ligand; CFU: Colony forming unit; CKO: Conditional knock out; CXCL: C-X-C motif ligand; Dpi: Days post-infection; ECAR: Extracellular acidification rate; EGFP: Enhanced green fluorescent protein; FOXO3: Forkhead box O3; GABA: Gamma-aminobutyric acid; GABAAR: GABA type A receptor; Gabarap: GABA type A receptor-associated protein; Gabarapl1: GABA type A receptor-associated protein like 1; GABRA4: Gamma-aminobutyric acid type A receptor subunit alpha4; HIF-1α: Hypoxia-inducible factor-1 alpha; IL: Interleukin; i.n.: Intranasal; i.p.: Intraperitoneal; LDHA: Lactate dehydrogenase A; LPS: Lipopolysaccharide; Mabc: Mycobacteroides abscessus subsp. abscessus; MOI: Multiplicities of infection; Mtb: Mycobacterium tuberculosis; mtROS: Mitochondrial reactive oxygen species; OCR: Oxygen consumption rate; OXPHOS: Oxidative phosphorylation; PM: Peritoneal macrophage; TNF: Tumor necrosis factor; WT: Wild type.

γ-氨基丁酸A型受体α4协调自噬、炎症和免疫代谢,促进先天免疫激活
γ -氨基丁酸A型受体(GABAAR)是GABA的嗜离子受体,在巨噬细胞和神经系统中表达;然而,它在先天免疫中的作用尚不清楚。在此,我们发现髓系GABAAR亚基α4 (Gabra4)在感染和炎症过程中是自噬的关键调节因子和宿主先天防御的促进因子。髓系Gabra4缺乏导致感染期间分枝杆菌清除缺陷和感染性休克易感性增加。Gabra4缺失会加重炎症反应,抑制巨噬细胞在感染和炎症刺激下的自噬激活。在机制上,gabra4介导的信号通过细胞内钙释放和amp活化蛋白激酶(AMPK)信号激活导致巨噬细胞自噬上调,这是连接自噬和抗菌反应所必需的。此外,Gabra4需要产生线粒体活性氧,从而触发自噬和对分枝杆菌的抗菌反应。代谢组学分析表明,Gabra4对巨噬细胞的葡萄糖代谢和有氧糖酵解至关重要。我们的研究结果表明,髓细胞Gabra4协调自噬、炎症和免疫代谢,以促进先天宿主对致病和危险刺激的防御。缩写AM:肺泡巨噬细胞;AMPK: amp活化蛋白激酶;ASC:含有CARD的凋亡相关斑点样蛋白;ATP: 5'-三磷酸腺苷;BAL:支气管肺泡灌洗;卡介苗:牛分枝杆菌卡介苗;BMDM:骨髓源性巨噬细胞;CCL: CC基序趋化因子配体;CFU:菌落形成单位;CKO:条件击倒;CXCL: C-X-C基序配体;Dpi:感染后天数;ECAR:细胞外酸化速率;EGFP:增强绿色荧光蛋白;FOXO3:叉车箱O3;GABA: -氨基丁酸;GABAAR: GABAA型受体;Gabarap: GABA A型受体相关蛋白;Gabarapl1: GABA A型受体相关蛋白样1;GABRA4: γ -氨基丁酸A型受体亚基α 4;HIF-1α:缺氧诱导因子-1α;IL:白介素;i.n:鼻内;i.p:腹腔内;乳酸脱氢酶A;有限合伙人:脂多糖;Mabc:脓肿分枝杆菌亚种。脓肿;MOI:感染的多样性;Mtb:结核分枝杆菌;mtROS:线粒体活性氧;OCR:耗氧量;OXPHOS:氧化磷酸化;PM:腹腔巨噬细胞;TNF:肿瘤坏死因子;WT:野生型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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