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 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.
Original language | English |
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Pages (from-to) | 875-880 |
Number of pages | 6 |
Journal | Biochemical and biophysical research communications |
Volume | 514 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2019 Jun 30 |
Bibliographical note
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 ).
Keywords
- AIMP1
- Calcium flux
- Lipid raft
- TCR signal
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology