LBAI, UMR1227, Univ Brest, Inserm, Brest, France.
Service d'Odontologie, CHU de Brest, Brest, France.
Front Immunol. 2021 Sep 28;12:735463. doi: 10.3389/fimmu.2021.735463. eCollection 2021.
Metabolic pathways have been studied for a while in eukaryotic cells. During glycolysis, glucose enters into the cells through the Glut1 transporter to be phosphorylated and metabolized generating ATP molecules. Immune cells can use additional pathways to adapt their energetic needs. The pentose phosphate pathway, the glutaminolysis, the fatty acid oxidation and the oxidative phosphorylation generate additional metabolites to respond to the physiological requirements. Specifically, in B lymphocytes, these pathways are activated to meet energetic demands in relation to their maturation status and their functional orientation (tolerance, effector or regulatory activities). These metabolic programs are differentially involved depending on the receptors and the co-activation molecules stimulated. Their induction may also vary according to the influence of the microenvironment, i.e. the presence of T cells, cytokines … promoting the expression of particular transcription factors that direct the energetic program and modulate the number of ATP molecule produced. The current review provides recent advances showing the underestimated influence of the metabolic pathways in the control of the B cell physiology, with a particular focus on the regulatory B cells, but also in the oncogenic and autoimmune evolution of the B cells.
代谢途径在真核细胞中已经被研究了一段时间。在糖酵解过程中,葡萄糖通过 Glut1 转运体进入细胞,被磷酸化并代谢生成 ATP 分子。免疫细胞可以利用其他途径来适应其能量需求。戊糖磷酸途径、谷氨酰胺分解代谢、脂肪酸氧化和氧化磷酸化会产生额外的代谢物,以响应生理需求。具体来说,在 B 淋巴细胞中,这些途径被激活以满足与其成熟状态和功能定向(耐受性、效应器或调节活性)相关的能量需求。这些代谢途径的诱导取决于所刺激的受体和共激活分子的不同而有所差异。它们的诱导也可能根据微环境的影响而变化,例如 T 细胞的存在、细胞因子等,这些因素促进了特定转录因子的表达,这些转录因子指导着能量程序,并调节产生的 ATP 分子的数量。本综述提供了最新进展,表明代谢途径在控制 B 细胞生理方面的影响被低估了,特别是在调节性 B 细胞方面,但也在 B 细胞的致癌和自身免疫演变方面。