Control of immune cell function by the unfolded protein response

被引:54
作者
Di Conza, Giusy [1 ,2 ]
Ho, Ping-Chih [1 ,2 ]
Cubillos-Ruiz, Juan R. [3 ,4 ,5 ]
Huang, Stanley Ching-Cheng [6 ,7 ]
机构
[1] Univ Lausanne, Dept Fundamental Oncol, Lausanne, Switzerland
[2] Univ Lausanne, Ludwig Inst Canc Res, Epalinges, Switzerland
[3] Weill Cornell Med, Dept Obstet & Gynecol, New York, NY 10021 USA
[4] Weill Cornell Med, Sandra & Edward Meyer Canc Ctr, New York, NY 10021 USA
[5] Weill Cornell Med, Grad Sch Med Sci, Immunol & Microbial Pathogenesis Program, New York, NY 10021 USA
[6] Case Western Reserve Univ, Dept Pathol, Sch Med, Cleveland, OH 44106 USA
[7] Case Western Reserve Univ, Case Comprehens Canc Ctr, Sch Med, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
ENDOPLASMIC-RETICULUM STRESS; SODIUM 4-PHENYLBUTYRATE PROTECTS; TRANSCRIPTION FACTOR XBP1; ER-STRESS; TRANSMEMBRANE PROTEIN; HEXOSAMINE PATHWAY; SENSOR IRE1-ALPHA; DENDRITIC CELLS; QUALITY-CONTROL; MESSENGER-RNA;
D O I
10.1038/s41577-023-00838-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Initiating and maintaining optimal immune responses requires high levels of protein synthesis, folding, modification and trafficking in leukocytes, which are processes orchestrated by the endoplasmic reticulum. Importantly, diverse extracellular and intracellular conditions can compromise the protein-handling capacity of this organelle, inducing a state of 'endoplasmic reticulum stress' that activates the unfolded protein response (UPR). Emerging evidence shows that physiological or pathological activation of the UPR can have effects on immune cell survival, metabolism, function and fate. In this Review, we discuss the canonical role of the adaptive UPR in immune cells and how dysregulation of this pathway in leukocytes contributes to diverse pathologies such as cancer, autoimmunity and metabolic disorders. Furthermore, we provide an overview as to how pharmacological approaches that modulate the UPR could be harnessed to control or activate immune cell function in disease.
引用
收藏
页码:546 / 562
页数:17
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