T-cell immunosuppression in sepsis is augmented by sciatic denervation-induced skeletal muscle atrophy.
Sumika OsaYuki EnokiDaisuke TakahashiVictor Tuan Giam ChuangKazuaki TaguchiKazuaki MatsumotoPublished in: FEBS letters (2024)
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.
Keyphrases
- skeletal muscle
- regulatory t cells
- septic shock
- acute kidney injury
- insulin resistance
- intensive care unit
- poor prognosis
- high fat diet induced
- flow cytometry
- long non coding rna
- high glucose
- magnetic resonance
- clinical trial
- induced apoptosis
- type diabetes
- computed tomography
- diabetic rats
- magnetic resonance imaging
- body mass index
- cell death
- ultrasound guided
- spinal cord
- high resolution
- endothelial cells
- metabolic syndrome
- mass spectrometry
- oxidative stress
- cell proliferation
- contrast enhanced
- wild type