The cGAS-STING pathway drives neuroinflammation and neurodegeneration via cellular and molecular mechanisms in neurodegenerative diseases

被引:10
作者
Zhang, Yuxin [1 ]
Zou, Meijuan [1 ]
Wu, Hao [1 ]
Zhu, Jie [1 ,2 ]
Jin, Tao [1 ]
机构
[1] First Hosp Jilin Univ, Neurosci Ctr, Dept Neurol, Changchun, Peoples R China
[2] Karolinska Univ Hosp Solna, Karolinska Inst, Dept Neurobiol Care Sci & Soc, Stockholm, Sweden
基金
中国国家自然科学基金;
关键词
cGAS-STING; Microglia; Astrocyte; Neuron; Innate immune system; Adaptive immune system; Neurodegenerative diseases; CYCLIC GMP-AMP; CYTOSOLIC DNA SENSOR; MITOCHONDRIAL DYSFUNCTION; MOUSE MODEL; T-CELLS; ATTENUATES NEUROINFLAMMATION; PARKINSONS-DISEASE; DENDRITIC CELLS; B-CELLS; ACTIVATION;
D O I
10.1016/j.nbd.2024.106710
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurodegenerative diseases (NDs) are a type of common chronic progressive disorders characterized by progressive damage to specific cell populations in the nervous system, ultimately leading to disability or death. Effective treatments for these diseases are still lacking, due to a limited understanding of their pathogeneses, which involve multiple cellular and molecular pathways. The triggering of an immune response is a common feature in neurodegenerative disorders. A critical challenge is the intricate interplay between neuroinflammation, neurodegeneration, and immune responses, which are not yet fully characterized. In recent years, the cyclic GMP-AMP synthase (cGAS)-stimulator of interferon gene (STING) pathway, a crucial immune response for intracellular DNA sensing, has gradually gained attention. However, the specific roles of this pathway within cellular types such as immune cells, glial and neuronal cells, and its contribution to ND pathogenesis, remain not fully elucidated. In this review, we systematically explore how the cGAS-STING signaling links various cell types with related cellular effector pathways under the context of NDs for multifaceted therapeutic directions. We emphasize the discovery of condition-dependent cellular heterogeneity in the cGAS-STING pathway, which is integral for understanding the diverse cellular responses and potential therapeutic targets. Additionally, we review the pathogenic role of cGAS-STING activation in Parkinson's disease, ataxia-telangiectasia, and amyotrophic lateral sclerosis. We focus on the complex bidirectional roles of the cGAS-STING pathway in Alzheimer's disease, Huntington's disease, and multiple sclerosis, revealing their double-edged nature in disease progression. The objective of this review is to elucidate the pivotal role of the cGAS-STING pathway in ND pathogenesis and catalyze new insights for facilitating the development of novel therapeutic strategies.
引用
收藏
页数:33
相关论文
共 396 条
[51]   LC3-Associated Phagocytosis in Myeloid Cells Promotes Tumor Immune Tolerance [J].
Cunha, Larissa D. ;
Yang, Mao ;
Carter, Robert ;
Guy, Clifford ;
Harris, Lacie ;
Crawford, Jeremy C. ;
Quarato, Giovanni ;
Boada-Romero, Emilio ;
Kalkavan, Halime ;
Johnson, Michael Dl ;
Natarajan, Sivaraman ;
Turnis, Meghan E. ;
Finkelstein, David ;
Opferman, Joseph T. ;
Gawad, Charles ;
Green, Douglas R. .
CELL, 2018, 175 (02) :429-+
[52]   STING agonist cGAMP enhances anti-tumor activity of CAR-NK cells against pancreatic cancer [J].
Da, Yanyan ;
Liu, Yuxia ;
Hu, Yuan ;
Liu, Wenzeng ;
Ma, Junpeng ;
Lu, Nan ;
Zhang, Chengsheng ;
Zhang, Cai .
ONCOIMMUNOLOGY, 2022, 11 (01)
[53]   Ferroptotic damage promotes pancreatic tumorigenesis through a TMEM173/STING-dependent DNA sensor pathway [J].
Dai, Enyong ;
Han, Leng ;
Liu, Jiao ;
Xie, Yangchun ;
Zeh, Herbert J. ;
Kang, Rui ;
Bai, Lulu ;
Tang, Daolin .
NATURE COMMUNICATIONS, 2020, 11 (01)
[54]   A clinically-relevant STING agonist restrains human TH17 cell inflammatory profile [J].
Damasceno, Luis Eduardo Alves ;
Cunha, Thiago Mattar ;
Cunha, Fernando Queiroz ;
Sparwasser, Tim ;
Alves-Filho, Jose Carlos .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 124
[55]   Cellular senescence in normal physiology [J].
de Magalhes, Joo Pedro .
SCIENCE, 2024, 384 (6702) :1300-1301
[56]   Autophagy in inflammation, infection, and immunometabolism [J].
Deretic, Vojo .
IMMUNITY, 2021, 54 (03) :437-453
[57]   Activating cGAS-STING axis contributes to neuroinflammation in CVST mouse model and induces inflammasome activation and microglia pyroptosis [J].
Ding, Rui ;
Li, Haiyan ;
Liu, Yaqi ;
Ou, Weiyang ;
Zhang, Xifang ;
Chai, Huihui ;
Huang, Xiaofei ;
Yang, Weijie ;
Wang, Qiujing .
JOURNAL OF NEUROINFLAMMATION, 2022, 19 (01)
[58]   STING Activation by Translocation from the ER Is Associated with Infection and Autoinflammatory Disease [J].
Dobbs, Nicole ;
Burnaevskiy, Nikolay ;
Chen, Didi ;
Gonugunta, Vijay K. ;
Alto, Neal M. ;
Yan, Nan .
CELL HOST & MICROBE, 2015, 18 (02) :157-168
[59]   STING controls nociception via type I interferon signalling in sensory neurons [J].
Donnelly, Christopher R. ;
Jiang, Changyu ;
Andriessen, Amanda S. ;
Wang, Kaiyuan ;
Wang, Zilong ;
Ding, Huiping ;
Zhao, Junli ;
Luo, Xin ;
Lee, Michael S. ;
Lei, Yu L. ;
Maixner, William ;
Ko, Mei-Chuan ;
Ji, Ru-Rong .
NATURE, 2021, 591 (7849) :275-+
[60]   Therapeutic targeting of STING-TBK1-IRF3 signalling ameliorates chronic stress induced depression-like behaviours by modulating neuroinflammation and microglia phagocytosis [J].
Duan, Na ;
Zhang, Yanpeng ;
Tan, Shuwen ;
Sun, Jianyu ;
Ye, Mao ;
Gao, Hui ;
Pu, Kairui ;
Wu, Meiyan ;
Wang, Qiang ;
Zhai, Qian .
NEUROBIOLOGY OF DISEASE, 2022, 169