坐骨神经支配引起的骨骼肌萎缩增强了败血症中的 T 细胞免疫抑制。

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology FEBS Letters Pub Date : 2024-08-08 DOI:10.1002/1873-3468.14999
Sumika Osa, Yuki Enoki, Daisuke Takahashi, Victor Tuan Giam Chuang, Kazuaki Taguchi, Kazuaki Matsumoto
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引用次数: 0

摘要

已知骨骼肌萎缩是导致免疫抑制和败血症预后不良的危险因素。然而,其免疫病理学尚未在实验中得到阐明。本研究调查了骨骼肌萎缩对败血症免疫病理学的影响。雄性 C57BL/6J 小鼠接受坐骨神经去神经(DN)和盲肠结扎穿刺(CLP)诱导肌肉萎缩或败血症。使用流式细胞术分析了腹膜和脾脏中的巨噬细胞、髓源抑制细胞(MDSC)和T细胞。DN诱导的肌肉萎缩不会影响巨噬细胞和MDSC的数量。相反,DN-CLP小鼠的细胞毒性T淋巴细胞相关抗原(CTLA)-4+ CD4+T细胞、程序性死亡(PD)-1+ CD8+T细胞、调节性T细胞和CTLA-4+调节性T细胞的百分比在统计学上明显高于假CLP小鼠。脓毒症前骨骼肌萎缩会引发过度的T细胞免疫抑制,这可能是骨骼肌萎缩导致脓毒症恶化的原因之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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T-cell immunosuppression in sepsis is augmented by sciatic denervation-induced skeletal muscle atrophy

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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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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