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代谢重编程调控免疫细胞功能。

Regulation of Immune Cell Functions by Metabolic Reprogramming.

机构信息

Department of Biochemistry, School of Medicine, Gachon University, Incheon 21999, Republic of Korea.

Department of Health Sciences and Technology, Gachon Advanced Institute for Health Science and Technology, Gachon University, Incheon 21999, Republic of Korea.

出版信息

J Immunol Res. 2018 Feb 13;2018:8605471. doi: 10.1155/2018/8605471. eCollection 2018.

Abstract

Recent findings show that the metabolic status of immune cells can determine immune responses. Metabolic reprogramming between aerobic glycolysis and oxidative phosphorylation, previously speculated as exclusively observable in cancer cells, exists in various types of immune and stromal cells in many different pathological conditions other than cancer. The microenvironments of cancer, obese adipose, and wound-repairing tissues share common features of inflammatory reactions. In addition, the metabolic changes in macrophages and T cells are now regarded as crucial for the functional plasticity of the immune cells and responsible for the progression and regression of many pathological processes, notably cancer. It is possible that metabolic changes in the microenvironment induced by other cellular components are responsible for the functional plasticity of immune cells. This review explores the molecular mechanisms responsible for metabolic reprogramming in macrophages and T cells and also provides a summary of recent updates with regard to the functional modulation of the immune cells by metabolic changes in the microenvironment, notably the tumor microenvironment.

摘要

最近的研究结果表明,免疫细胞的代谢状态可以决定免疫反应。有氧糖酵解和氧化磷酸化之间的代谢重编程,以前被推测仅在癌细胞中观察到,在除癌症以外的许多不同病理条件下的各种免疫和基质细胞中都存在。癌症、肥胖脂肪和伤口修复组织的微环境具有炎症反应的共同特征。此外,巨噬细胞和 T 细胞的代谢变化现在被认为对免疫细胞的功能可塑性至关重要,并负责许多病理过程的进展和消退,特别是癌症。微环境中其他细胞成分引起的代谢变化可能负责免疫细胞的功能可塑性。这篇综述探讨了巨噬细胞和 T 细胞中代谢重编程的分子机制,并对近年来关于微环境(特别是肿瘤微环境)中代谢变化对免疫细胞功能的调节的最新进展进行了总结。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2b3e/5831954/02faa334b043/JIR2018-8605471.001.jpg

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