Kong Dejun, WillsonShirkey Marina, Piao Wenji, Wu Long, Luo Shunqun, Kensiski Allision, Zhao Jing, Lee Young, Abdi Reza, Zheng Hong, Bromberg Jonathan S
Center for Vascular and Inflammatory Diseases, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Tianjin Organ Transplantation Research Center, Nankai University affiliated Tianjin First Central Hospital, Nankai University School of Medicine, Tianjin, China.
Eur J Immunol. 2025 Jan;55(1):e202451321. doi: 10.1002/eji.202451321. Epub 2024 Nov 18.
Fibroblastic reticular cells (FRCs) are pivotal stromal components that maintain the structure of secondary lymphoid tissues and modulate the immune responses within the lymphoid microenvironment. In response to specific immune or inflammatory stimuli, such as infection or autoimmune triggers, FRCs undergo significant metabolic reprogramming. This process, originally characterized in cancer research, involves the regulation of key metabolic enzymes, pathways, and metabolites, resulting in functional transformations of these cells. Specifically, viruses stimulate FRCs to enhance the tricarboxylic acid cycle, while rheumatoid arthritis and sepsis prompt FRCs to increase oxidative phosphorylation. These changes enable FRCs to adapt their functions, such as proliferation or cytokine secretion, thereby effectively regulating the immune microenvironment to meet the dynamic needs of the immune system. This review provides a comprehensive update on the metabolic reprogramming of FRCs, highlighting how these changes support immune tolerance and response under varied physiological conditions.
成纤维网状细胞(FRCs)是关键的基质成分,维持次级淋巴组织的结构并调节淋巴微环境内的免疫反应。响应特定的免疫或炎症刺激,如感染或自身免疫触发因素,FRCs会经历显著的代谢重编程。这一过程最初在癌症研究中得以描述,涉及关键代谢酶、途径和代谢物的调控,导致这些细胞发生功能转变。具体而言,病毒刺激FRCs增强三羧酸循环,而类风湿性关节炎和败血症促使FRCs增加氧化磷酸化。这些变化使FRCs能够调整其功能,如增殖或细胞因子分泌,从而有效调节免疫微环境以满足免疫系统的动态需求。本综述全面更新了FRCs的代谢重编程,强调了这些变化如何在不同生理条件下支持免疫耐受和反应。