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
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