Ro5-4864, a translocator protein ligand, regulates T cell-mediated inflammatory responses in skin

Translocator protein (TSPO) is a mitochondrial outer membrane protein expressed on a variety of immune cells, including macrophages, dendritic cells, and T cells, in addition to neurons and steroid-producing cells. Previous studies of TSPO ligands have suggested that TSPO is involved in multiple cellular functions, including steroidogenesis, immunomodulation, and cell proliferation. Currently, there are limited reports on the effects of TSPO or TSPO ligands on T cell-mediated immune responses. Here, we investigated the involvement of TSPO/TSPO ligand in T cell responses using a 2,4-dinitro-1-fluorobenzene (DNFB)-induced contact hypersensitivity (CH) model. Treatment with Ro5-4864, a TSPO ligand, during DNFB sensitization reduced the number and activation status of CD4+ and CD8+ T cells in draining lymph nodes and alleviated skin inflammation after DNFB challenge. Adoptive transfer of Ro5-4864-treated mouse-derived DNFB-sensitized T cells to naive mice inhibited CH responses after DNFB challenge. Ro5-4864-treated sensitized T cells showed lower proliferative responses when stimulated with DNFB-pulsed antigen-presenting cells compared to control-treated sensitized T cells. Ro5-4864 also suppressed cell proliferation, as well as adenosine triphosphate and lactate production, during T cell activation. Moreover, the inhibitory effects of Ro5-4864 on T cell responses were conserved in TSPO-deficient cells. Our results suggest that Ro5-4864 inhibits CH responses by suppressing energy metabolism, at least via glycolysis, to reduce the T cell primary response in a TSPO-independent manner.

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Journal
International Immunology
Published
2024-10-26
DOI
https://doi.org/10.1093/intimm/dxae065
Citations
1
Primary Topic
Immune Response and Inflammation
Type
article
Field-Weighted Citation Impact
0.24

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article

Ro5-4864, a translocator protein ligand, regulates T cell-mediated inflammatory responses in skin

Makoto Higuchi, Kyotaro Koshika, Tatsuya Ichinohe, Keisuke Ohta et al.
1 citations
International Immunology
Immune Response and Inflammation
0.24
article

Ro5-4864, a translocator protein ligand, regulates T cell-mediated inflammatory responses in skin

Makoto Higuchi, Kyotaro Koshika, Tatsuya Ichinohe, Keisuke Ohta, Kei Kitamura, Susumu Nakae, Kazuyoshi Takeda, Tatsukuni Ohno, Ko Okumura, Yuka Sendai, Toshifumi Azuma
article en
1 citations

Abstract

Translocator protein (TSPO) is a mitochondrial outer membrane protein expressed on a variety of immune cells, including macrophages, dendritic cells, and T cells, in addition to neurons and steroid-producing cells. Previous studies of TSPO ligands have suggested that TSPO is involved in multiple cellular functions, including steroidogenesis, immunomodulation, and cell proliferation. Currently, there are limited reports on the effects of TSPO or TSPO ligands on T cell-mediated immune responses. Here, we investigated the involvement of TSPO/TSPO ligand in T cell responses using a 2,4-dinitro-1-fluorobenzene (DNFB)-induced contact hypersensitivity (CH) model. Treatment with Ro5-4864, a TSPO ligand, during DNFB sensitization reduced the number and activation status of CD4+ and CD8+ T cells in draining lymph nodes and alleviated skin inflammation after DNFB challenge. Adoptive transfer of Ro5-4864-treated mouse-derived DNFB-sensitized T cells to naive mice inhibited CH responses after DNFB challenge. Ro5-4864-treated sensitized T cells showed lower proliferative responses when stimulated with DNFB-pulsed antigen-presenting cells compared to control-treated sensitized T cells. Ro5-4864 also suppressed cell proliferation, as well as adenosine triphosphate and lactate production, during T cell activation. Moreover, the inhibitory effects of Ro5-4864 on T cell responses were conserved in TSPO-deficient cells. Our results suggest that Ro5-4864 inhibits CH responses by suppressing energy metabolism, at least via glycolysis, to reduce the T cell primary response in a TSPO-independent manner.

International ImmunologyVol. 37(4)
Kurume University (JP), Hiroshima University (JP), Tokyo Dental College (JP), Juntendo University (JP), National Institutes for Quantum Science and Technology (JP)
Japan Society for the Promotion of Science
Affordable and clean energy
Openalex Percentile: Top 41%
Immune Response and Inflammation
0.24
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