Key Laboratory of Aquacultural Biotechnology Ministry of Education, and Key Laboratory of Marine Biotechnology of Zhejiang Province, College of Marine Sciences, Ningbo University, Ningbo, Zhejiang, China.
Zhejiang Key Laboratory of Aquatic Germplasm Resources, Ningbo Academy of Oceanology and Fishery, Ningbo, Zhejiang, China.
Front Immunol. 2024 Aug 2;15:1410082. doi: 10.3389/fimmu.2024.1410082. eCollection 2024.
The immune system requires a high energy expenditure to resist pathogen invasion. Macrophages undergo metabolic reprogramming to meet these energy requirements and immunologic activity and polarize to M1-type macrophages. Understanding the metabolic pathway switching in large yellow croaker () macrophages in response to lipopolysaccharide (LPS) stimulation and whether this switching affects immunity is helpful in explaining the stronger immunity of hypoxia-tolerant . In this study, transcript levels of glycolytic pathway genes ( and ), mRNA levels or enzyme activities of glycolytic enzymes [hexokinase (HK), phosphofructokinase (PFK), pyruvate kinase (PK), and lactate dehydrogenase A (LDHA)], aerobic respiratory enzymes [pyruvate dehydrogenase (PDH), isocitrate dehydrogenase (IDH), and succinate dehydrogenase (SDH)], metabolites [lactic acid (LA) and adenosine triphosphate (ATP)], levels of bactericidal products [reactive oxygen species (ROS) and nitric oxide (NO)], and transcripts and level changes of inflammatory factors [IL1β, TNFα, and interferon (IFN) γ] were detected in LPS-stimulated head kidney macrophages. We showed that glycolysis was significantly induced, the tricarboxylic acid (TCA) cycle was inhibited, and metabolic reprogramming occurred, showing the Warburg effect when immune cells were activated. To determine the potential regulatory mechanism behind these changes, HIF-1α was detected and found to be significantly induced and transferred to the nucleus after LPS stimulation. interference led to a significant reduction in glycolytic pathway gene transcript expression, enzyme activity, metabolites, bactericidal substances, and inflammatory factor levels; a significant increase in the aerobic respiration enzymes; and decreased migration, invasion, and phagocytosis. Further ultrastructural observation by electron microscopy showed that fewer microspheres contained phagocytes and that more cells were damaged after interference. overexpression head kidney macrophages showed the opposite trend, and promoter activities of and were significantly enhanced after overexpression in HEK293T cells. Our data showed that HIF-1α acted as a metabolic switch in macrophages and was important in polarization. Hypoxia-tolerant head kidney showed a stronger Warburg effect and inhibited the TCA cycle, higher metabolites, and bactericidal substance levels. These results collectively revealed that may promote the functional activities of head kidney macrophages in protecting hypoxia-tolerant from infection.
免疫系统需要高能量消耗来抵抗病原体入侵。巨噬细胞经历代谢重编程以满足这些能量需求和免疫活性,并极化到 M1 型巨噬细胞。了解大黄鱼()巨噬细胞对脂多糖(LPS)刺激的代谢途径转换,以及这种转换是否影响免疫,有助于解释耐缺氧大黄鱼更强的免疫力。在这项研究中,检测了糖酵解途径基因(和)的转录水平、糖酵解酶[己糖激酶(HK)、磷酸果糖激酶(PFK)、丙酮酸激酶(PK)和乳酸脱氢酶 A(LDHA)]的 mRNA 水平或酶活性、有氧呼吸酶[丙酮酸脱氢酶(PDH)、异柠檬酸脱氢酶(IDH)和琥珀酸脱氢酶(SDH)]、代谢物[乳酸(LA)和三磷酸腺苷(ATP)]、杀菌产物[活性氧(ROS)和一氧化氮(NO)]的水平,以及炎症因子[白细胞介素 1β(IL1β)、肿瘤坏死因子α(TNFα)和干扰素(IFN)γ]的转录和水平变化,在 LPS 刺激的大黄鱼头肾巨噬细胞中进行检测。我们表明,当免疫细胞被激活时,糖酵解明显被诱导,三羧酸(TCA)循环被抑制,代谢重编程发生,表现出沃伯格效应。为了确定这些变化背后的潜在调节机制,检测到 HIF-1α 并发现其在 LPS 刺激后显著诱导并转移到核内。干扰导致糖酵解途径基因转录表达、酶活性、代谢物、杀菌物质和炎症因子水平的显著降低,有氧呼吸酶的显著增加,以及迁移、侵袭和吞噬作用的减少。电子显微镜的进一步超微结构观察表明,干扰后含有吞噬细胞的微球减少,更多的细胞受损。过表达大黄鱼头肾巨噬细胞表现出相反的趋势,并且在 HEK293T 细胞中过表达后,和的启动子活性显著增强。我们的数据表明,HIF-1α 在大黄鱼巨噬细胞中充当代谢开关,在极化中很重要。耐缺氧大黄鱼头肾表现出更强的沃伯格效应,抑制 TCA 循环,更高的代谢物和杀菌物质水平。这些结果共同表明,可能促进耐缺氧大黄鱼头肾巨噬细胞保护其免受感染的功能活动。