TY - JOUR
T1 - AIMP1 regulates TCR signaling and induces differentiation of regulatory T cells by interfering with lipid raft association
AU - Kim, Myun Soo
AU - Lee, Arim
AU - Cho, Daeho
AU - Kim, Tae Sung
N1 - Funding Information:
This work was supported by the National Research Foundation of Korea (NRF)grant (NRF-2017R1A2B2009442).
Funding Information:
This work was supported by the National Research Foundation of Korea ( NRF ) grant ( NRF-2017R1A2B2009442 ).
PY - 2019/6/30
Y1 - 2019/6/30
N2 - 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 PLCγ 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.
AB - 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 PLCγ 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.
KW - AIMP1
KW - Calcium flux
KW - Lipid raft
KW - TCR signal
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U2 - 10.1016/j.bbrc.2019.05.040
DO - 10.1016/j.bbrc.2019.05.040
M3 - Article
C2 - 31084930
AN - SCOPUS:85065409957
SN - 0006-291X
VL - 514
SP - 875
EP - 880
JO - Biochemical and biophysical research communications
JF - Biochemical and biophysical research communications
IS - 3
ER -