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AIMP1 regulates TCR signaling and induces differentiation of regulatory T cells by interfering with lipid raft association

Authors
Kim, Myun SooLee, ArimCho, DaehoKim, Tae Sung
Issue Date
30-6월-2019
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
AIMP1; TCR signal; Calcium flux; Lipid raft
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.514, no.3, pp.875 - 880
Indexed
SCIE
SCOPUS
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
514
Number
3
Start Page
875
End Page
880
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/64718
DOI
10.1016/j.bbrc.2019.05.040
ISSN
0006-291X
Abstract
In addition to a role in translation, AIMP1 is secreted to affect various immune cells, such as macrophages, dendritic cells, B cells, and natural killer cells. However, the direct effects of AIMP1 on T cells have not yet been reported. In this study, we investigated whether AIMP1 could modulate T cell responses directly. Results revealed that AIMP1 significantly inhibited T cell receptor (TCR)-dependent activation and proliferation of CD4 T cells, as well as decreased TCR stimuli-induced Ca2+ influx in CD4 T cells. In addition, microscopic analysis revealed that lipid raft association in response to TCR engagement was significantly reduced in the presence of AIMP1, and the phosphorylation of PLC gamma and PI3K was also down-regulated in CD4 T cells by AIMP1. Furthermore, AIMP1 specifically enhanced the differentiation of regulatory T (Treg) cells, while it had no effect on T helper type 1 (Th1), type 2 (Th2), and type 17 (Th17) cell differentiation. Collectively, these results indicate that AIMP1 affects T cells directly by down-regulating TCR signaling complex formation and inducing Treg cell differentiation in CD4 T cells. (C) 2019 Elsevier Inc. All rights reserved.
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