a MRC Weatherall Institute of Molecular Medicine , Nuffield Department of Medicine, University of Oxford, John Radcliffe Hospital , Headington , Oxford , UK.
b Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences , University of Oxford , Oxford , UK.
Autophagy. 2018;14(2):199-206. doi: 10.1080/15548627.2017.1362525. Epub 2017 Sep 13.
The role of macroautophagy/autophagy, a conserved lysosomal degradation pathway, during cellular differentiation has been well studied over the last decade. In particular, evidence for its role during immune cell differentiation is growing. Despite the description of a variety of dramatic immune phenotypes in tissue-specific autophagy knockout models, the underlying mechanisms are still under debate. One of the proposed mechanisms is the impact of autophagy on the altered metabolic states during immune cell differentiation. This concept is strengthened through novel molecular insights into how AMPK and MTOR signaling cascades affect both autophagy and metabolism. In this review, we discuss direct and indirect evidence linking autophagy, metabolic pathways and immune cell differentiation including T, B, and innate lymphocytes as well as in myeloid cells that are direct mediators of inflammation. Herein, we propose a model for autophagy-driven immunometabolism controlling immune cell differentiation.
在过去的十年中,人们对巨自噬/自噬(一种保守的溶酶体降解途径)在细胞分化过程中的作用进行了深入研究。特别是,自噬在免疫细胞分化中的作用的证据正在不断增加。尽管在组织特异性自噬敲除模型中描述了各种剧烈的免疫表型,但潜在的机制仍存在争议。其中一个提出的机制是自噬对免疫细胞分化过程中代谢状态改变的影响。AMPK 和 MTOR 信号级联如何影响自噬和代谢的新分子见解进一步证实了这一概念。在这篇综述中,我们讨论了直接和间接证据,这些证据将自噬、代谢途径和免疫细胞分化联系起来,包括 T、B 和先天淋巴细胞,以及作为炎症直接介质的髓样细胞。在此,我们提出了一个自噬驱动的免疫代谢模型,用于控制免疫细胞分化。