Sim Wen Jing, Ahl Patricia Jennifer, Connolly John Edward
Institute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore 138673.
Institute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore 138673; Institute of Biomedical Studies, Baylor University, Waco, TX 76712, USA.
Mediators Inflamm. 2016;2016:2636701. doi: 10.1155/2016/2636701. Epub 2016 Feb 11.
Immunological tolerance is a fundamental tenant of immune homeostasis and overall health. Self-tolerance is a critical component of the immune system that allows for the recognition of self, resulting in hyporeactivity instead of immunogenicity. Dendritic cells are central to the establishment of dominant immune tolerance through the secretion of immunosuppressive cytokines and regulatory polarization of T cells. Cellular metabolism holds the key to determining DC immunogenic or tolerogenic cell fate. Recent studies have demonstrated that dendritic cell maturation leads to a shift toward a glycolytic metabolic state and preferred use of glucose as a carbon source. In contrast, tolerogenic dendritic cells favor oxidative phosphorylation and fatty acid oxidation. This dichotomous metabolic reprogramming of dendritic cells drives differential cellular function and plays a role in pathologies, such as autoimmune disease. Pharmacological alterations in metabolism have promising therapeutic potential.
免疫耐受是免疫稳态和整体健康的基本要素。自身耐受是免疫系统的关键组成部分,它能够识别自身,导致反应性降低而非免疫原性。树突状细胞通过分泌免疫抑制细胞因子和T细胞的调节性极化,在建立主导性免疫耐受中起核心作用。细胞代谢是决定树突状细胞免疫原性或耐受性细胞命运的关键。最近的研究表明,树突状细胞成熟会导致向糖酵解代谢状态转变,并优先使用葡萄糖作为碳源。相比之下,耐受性树突状细胞则倾向于氧化磷酸化和脂肪酸氧化。树突状细胞这种二分法的代谢重编程驱动了不同的细胞功能,并在诸如自身免疫性疾病等病理过程中发挥作用。代谢的药理学改变具有广阔的治疗潜力。