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T-cell immunosuppression in sepsis is augmented by sciatic denervation-induced skeletal muscle atrophy.
Osa, Sumika; Enoki, Yuki; Takahashi, Daisuke; Chuang, Victor Tuan Giam; Taguchi, Kazuaki; Matsumoto, Kazuaki.
Afiliação
  • Osa S; Division of Pharmacodynamics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Enoki Y; Division of Pharmacodynamics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Takahashi D; Division of Biochemistry, Graduate School of Pharmaceutical Sciences and Department of Pharmaceutical Sciences, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Chuang VTG; Discipline of Pharmacy, Curtin Medical School, Faculty of Health Sciences, Curtin University, Perth, Australia.
  • Taguchi K; Division of Pharmacodynamics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
  • Matsumoto K; Division of Pharmacodynamics, Faculty of Pharmacy, Keio University, Tokyo, Japan.
FEBS Lett ; 2024 Aug 08.
Article em En | MEDLINE | ID: mdl-39118298
ABSTRACT
Skeletal muscle atrophy is a known risk factor for immunosuppressive conditions and for a poor prognosis in sepsis. However, its immunopathology has not been experimentally elucidated. This study investigated the effects of skeletal muscle atrophy on the immunopathology of sepsis. Male C57BL/6J mice were subjected to sciatic denervation (DN) and caecal ligation and puncture (CLP) to induce muscle atrophy or sepsis. The macrophages, myeloid-derived suppressor cells (MDSC), and T-cells in peritoneal and spleen were analysed using flow cytometry. DN-induced muscle atrophy did not affect macrophage and MDSC populations. In contrast, the percentage of cytotoxic T-lymphocyte-associated antigen (CTLA)-4+ CD4+ T-cells, programmed death (PD)-1+ CD8+ T-cells, regulatory T-cells, and the CTLA-4+ regulatory T-cells was statistically significantly higher in DN-CLP mice than in sham-CLP mice. Skeletal muscle atrophy before sepsis triggers excessive T cell immunosuppression, which may contribute to the exacerbation of sepsis under skeletal muscle atrophy.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: FEBS Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: FEBS Lett Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão
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