类风湿性关节炎
医学
重编程
癌症研究
下调和上调
巨噬细胞
柠檬酸循环
炎症
细胞因子
关节炎
氧化磷酸化
免疫学
滑膜
代谢途径
药理学
滑液
促炎细胞因子
治疗方法
新陈代谢
表型
分泌物
炎性关节炎
细胞生物学
作者
Dahai Hu,Yaru Sun,Qi Lu,Yi Zhang,Yi Zhang,J Li,Huige Hou,Huajun Wang,Hui Tang,Yunsong Zhang,Yunsong Zhang,Xiaofei Zheng,Qingsong Mei
标识
DOI:10.1002/advs.202523949
摘要
Rheumatoid arthritis (RA) has always been a therapeutic challenge in clinical due to the lack of effective drug treatments. Inspired by the impact of daily diet on RA, herein we proposed an innovative energy metabolism modulation strategy to reprogram synovial macrophages for RA treatment. An implantable hydrogel, encapsulating with optogenetics-engineered cells, was designed to enable in-situ and on-demand secretion of glucagon-like peptide-1 (GLP-1) through blue light irradiation. GLP-1 in synovium was found to activate GLP-1R/HK2/VDAC1 pathway to upregulate the tricarboxylic acid cycle and oxidative phosphorylation in macrophages. This metabolic reprogramming elicited a phenotypic transition in macrophage polarization, shifting from M0/M1 state to M2 state. Significantly, the GLP-1-mediated approach reduced synovial inflammatory cytokine levels and facilitated tissue repair and bone erosion recovery. These findings reveal the therapeutic potential of GLP-1R/HK2/VDAC1 pathway as a novel target for RA.
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