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AIMP1 regulates TCR signaling and induces differentiation of regulatory T cells by interfering with lipid raft association.
Kim, Myun Soo; Lee, Arim; Cho, Daeho; Kim, Tae Sung.
Afiliación
  • Kim MS; Institute of Convergence Science, Korea University, 5-ga, Anam-dong, Seongbuk-gu, Seoul, 02841, Republic of Korea.
  • Lee A; Division of Life Sciences, College of Life Sciences and Biotechnology, Korea University, 5-ga, Anam-dong, Seongbuk-gu, Seoul, 02841, Republic of Korea.
  • Cho D; Institute of Convergence Science, Korea University, 5-ga, Anam-dong, Seongbuk-gu, Seoul, 02841, Republic of Korea.
  • Kim TS; Division of Life Sciences, College of Life Sciences and Biotechnology, Korea University, 5-ga, Anam-dong, Seongbuk-gu, Seoul, 02841, Republic of Korea. Electronic address: tskim@korea.ac.kr.
Biochem Biophys Res Commun ; 514(3): 875-880, 2019 06 30.
Article en En | MEDLINE | ID: mdl-31084930
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Activación de Linfocitos / Receptores de Antígenos de Linfocitos T / Transducción de Señal / Citocinas / Linfocitos T Reguladores / Microdominios de Membrana Tipo de estudio: Risk_factors_studies Idioma: En Revista: Biochem Biophys Res Commun Año: 2019 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Activación de Linfocitos / Receptores de Antígenos de Linfocitos T / Transducción de Señal / Citocinas / Linfocitos T Reguladores / Microdominios de Membrana Tipo de estudio: Risk_factors_studies Idioma: En Revista: Biochem Biophys Res Commun Año: 2019 Tipo del documento: Article