Charge-based immunoreceptor signalling in health and disease

被引:1
作者
Shi, Xiaoshan [1 ]
He, Xing [2 ]
Xu, Chenqi [2 ]
机构
[1] Chinese Acad Sci, Shenzhen Inst Synthet Biol, Shenzhen Inst Adv Technol, Key Lab Quantitat Synthet Biol, Shenzhen, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Biochem & Cell Biol, CAS Ctr Excellence Mol Cell Sci, Key Lab Multicell Syst, Shanghai, Peoples R China
关键词
CELL-RECEPTOR ZETA; COMMON VARIABLE IMMUNODEFICIENCY; PROTEIN-TYROSINE KINASES; T-CELLS; CYTOPLASMIC DOMAIN; TRANSMEMBRANE ACTIVATOR; IMMUNOLOGICAL SYNAPSE; MEMBRANE ASSOCIATION; SUBUNIT CONTAINS; CODING VARIANTS;
D O I
10.1038/s41577-024-01105-6
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunoreceptors have crucial roles in sensing environmental signals and initiating immune responses to protect the host. Dysregulation of immunoreceptor signalling can therefore lead to a range of diseases, making immunoreceptor-based therapies a promising frontier in biomedicine. A common feature of various immunoreceptors is the basic-residue-rich sequence (BRS), which is a largely unexplored aspect of immunoreceptor signalling. The BRS is typically located in the cytoplasmic juxtamembrane region of immunoreceptors, where it forms dynamic interactions with neighbouring charged molecules to regulate signalling. Loss or gain of the basic residues in an immunoreceptor BRS has been linked to severe human diseases, such as immunodeficiency and autoimmunity. In this Perspective, we describe the role of BRSs in various immunoreceptors, elucidating their signalling mechanisms and biological functions. Furthermore, we highlight pathogenic mutations in immunoreceptor BRSs and discuss the potential of leveraging BRS signalling in engineered T cell-based therapies. The basic-residue-rich sequence (BRS) is a common motif located in the cytoplasmic tail of most immunoreceptors. This Perspective highlights the mechanisms of BRS signalling, its pathophysiological importance and how to harness BRS signalling to develop next-generation immunotherapy.
引用
收藏
页码:298 / 311
页数:14
相关论文
共 162 条
[51]   Lipid-dependent conformational dynamics underlie the functional versatility of T-cell receptor [J].
Guo, Xingdong ;
Yan, Chengsong ;
Li, Hua ;
Huang, Wenmao ;
Shi, Xiaoshan ;
Huang, Min ;
Wang, Yingfang ;
Pan, Weiling ;
Cai, Mingjun ;
Li, Lunyi ;
Wu, Wei ;
Bai, Yibing ;
Zhang, Chi ;
Liu, Zhijun ;
Wang, Xinyan ;
Zhang, Xiaohui F. ;
Tang, Chun ;
Wang, Hongda ;
Liu, Wanli ;
Ouyang, Bo ;
Wong, Catherine C. ;
Cao, Yi ;
Xu, Chenqi .
CELL RESEARCH, 2017, 27 (04) :505-525
[52]   LAG3 associates with TCR-CD3 complexes and suppresses signaling by driving co-receptor-Lck dissociation [J].
Guy, Clifford ;
Mitrea, Diana M. ;
Chou, Po-Chien ;
Temirov, Jamshid ;
Vignali, Kate M. ;
Liu, Xueyan ;
Zhang, Hui ;
Kriwacki, Richard ;
Bruchez, Marcel P. ;
Watkins, Simon C. ;
Workman, Creg J. ;
Vignali, Dario A. A. .
NATURE IMMUNOLOGY, 2022, 23 (05) :757-+
[53]   Design principles of PI(4,5)P2 clustering under protein-free conditions: Specific cation effects and calcium-potassium synergy [J].
Han, Kyungreem ;
Kim, Soon Ho ;
Venable, Richard M. ;
Pastor, Richard W. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2022, 119 (22)
[54]   Combination of metabolic intervention and T cell therapy enhances solid tumor immunotherapy [J].
Hao, Meixi ;
Hou, Siyuan ;
Li, Weishuo ;
Li, Kaiming ;
Xue, Lingjing ;
Hu, Qifan ;
Zhu, Lulu ;
Chen, Yue ;
Sun, Hongbin ;
Ju, Caoyun ;
Zhang, Can .
SCIENCE TRANSLATIONAL MEDICINE, 2020, 12 (571)
[55]   Noncanonical binding of Lck to CD3ε promotes TCR signaling and CAR function [J].
Hartl, Frederike A. ;
Beck-Garcia, Esmeralda ;
Woessner, Nadine M. ;
Flachsmann, Lea J. ;
Cardenas, Rubi M-H Velasco ;
Brandl, Simon M. ;
Taromi, Sanaz ;
Fiala, Gina J. ;
Morath, Anna ;
Mishra, Pankaj ;
Yousefi, O. Sascha ;
Zimmermann, Julia ;
Hoefflin, Nico ;
Koehn, Maja ;
Woehrl, Birgitta M. ;
Zeiser, Robert ;
Schweimer, Kristian ;
Guenther, Stefan ;
Schamel, Wolfgang W. ;
Minguet, Susana .
NATURE IMMUNOLOGY, 2020, 21 (08) :902-+
[56]   Intrinsically disordered cytoplasmic domains of two cytokine receptors mediate conserved interactions with membranes [J].
Haxholm, Gitte W. ;
Nikolajsen, Louise F. ;
Olsen, Johan G. ;
Fredsted, Jacob ;
Larsen, Flemming H. ;
Goffin, Vincent ;
Pedersen, Stine F. ;
Brooks, Andrew J. ;
Waters, Michael J. ;
Kragelund, Birthe B. .
BIOCHEMICAL JOURNAL, 2015, 468 :495-506
[57]   Top 10 Challenges in Cancer Immunotherapy [J].
Hegde, Priti S. ;
Chen, Daniel S. .
IMMUNITY, 2020, 52 (01) :17-35
[58]   CD45: A critical regulator of signaling thresholds in immune cells [J].
Hermiston, ML ;
Xu, Z ;
Weiss, A .
ANNUAL REVIEW OF IMMUNOLOGY, 2003, 21 :107-137
[59]   Cross-regulation of signaling by ITAM-associated receptors [J].
Ivashkiv, Lionel B. .
NATURE IMMUNOLOGY, 2009, 10 (04) :340-347
[60]   Saturation mutagenesis of the β subunit of the human granulocyte-macrophage colony-stimulating factor receptor shows clustering of constitutive mutations, activation of ERK MAP kinase and STAT pathways, and differential β subunit tyrosine phosphorylation [J].
Jenkins, BJ ;
Blake, TJ ;
Gonda, TJ .
BLOOD, 1998, 92 (06) :1989-2002