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Author Spotlight: Advanced Integrated Model for Sepsis-Induced Myopathy and Single-Cell Metabolic Analysis
Published on: June 14, 2024
Sepsis causes neutrophil infiltration in muscle leading to muscle atrophy and weakness in mice
Nobuto Nakanishi1, Yuko Ono1, Yusuke Miyazaki1
1Division of Disaster and Emergency Medicine, Department of Surgery Related, Kobe University Graduate School of Medicine, Kobe, Japan.
Background:
Sepsis-induced muscle atrophy leads to prolonged physical dysfunction. Although the interaction of muscle atrophy and macrophage has been reported in sepsis, the role of neutrophils in muscle atrophy has not been thoroughly investigated. This study sought to investigate the long-term changes in muscle-localized neutrophils after sepsis induction and their possible role in sepsis.
Methods:
Sepsis was induced in seven-week-old male C57BL/6J mice 8-12 (cecal slurry [CS] model) via intraperitoneal injection of 1 mg/g cecal slurry. The percentage change in body weight and grip strength was evaluated. The tibialis anterior muscles were dissected for microscopic examination of the cross-sectional area of myofibers or Fluorescence-activated cell sorting (FACS) analysis of immune cells. These changes were evaluated in the following conditions: (1) Longitudinal change until day 61, (2) CS concentration-dependent change on day 14 at the low (0.3 mg/g), middle (1.0 mg/g), and high (2.0 mg/g) concentrations, and (3) CS mice on day 14 treated with an anti-Ly6G antibody that depletes neutrophils.
Results:
Body weight and grip strength were significantly lower in the CS model until day 61 (body weight: 123.1% ± 1.8% vs. 130.3% ± 2.5%, p = 0.04; grip strength: 104.5% ± 3.8% vs. 119.3% ± 5.3%, p = 0.04). Likewise, cross-sectional muscle area gradually decreased until day 61 from the CS induction (895.6 [606.0-1304.9] μm2 vs. 718.8 [536.2-937.0] μm2, p < 0.01). The number of muscle-localized neutrophils increased from 2.3 ± 0.6 cell/mg on day 0 to 22.2 ± 13.0 cell/mg on day 14, and decreased thereafter. In terms of CS concentration-dependent change, cross-sectional area was smaller (484.4 ± 221.2 vs. 825.8 ± 436.2 μm2 [p < 0.001]) and grip strength was lower (71.4% ± 12.8% vs. 116.3% ± 7.4%, p = 0.01) in the CS High group compared with the control, with increased neutrophils (p = 0.03). Ly6G-depleted mice demonstrated significant increase of muscle cross-sectional area and grip strength compared with control mice (p < 0.01).
Conclusions:
Sepsis causes infiltration of neutrophils in muscles, leading to muscle atrophy and weakness. Depletion of neutrophils in muscle reverses sepsis-induced muscle atrophy and weakness. These results suggest that neutrophils may play a critical role in sepsis-induced muscle atrophy and weakness.
Insights
Sepsis causes muscle atrophy and weakness by increasing neutrophils in muscles. Depleting neutrophils reverses these effects, suggesting their critical role in sepsis-induced muscle dysfunction.
Area of Science:
- Immunology
- Skeletal Muscle Physiology
- Sepsis Pathophysiology
Background:
- Sepsis-induced muscle atrophy contributes to long-term physical dysfunction.
- While macrophage interactions in sepsis are known, neutrophil roles in muscle atrophy remain under-investigated.
Purpose of the Study:
- To investigate long-term changes in muscle-localized neutrophils post-sepsis.
- To determine the role of neutrophils in sepsis-induced muscle atrophy and weakness.
Main Methods:
- Sepsis was induced in mice using the cecal slurry (CS) model.
- Evaluated body weight, grip strength, and tibialis anterior muscle cross-sectional area.
- Analyzed muscle-infiltrating neutrophils using Fluorescence-activated cell sorting (FACS) and neutrophil depletion via anti-Ly6G antibody.
Main Results:
- Sepsis induced prolonged reductions in body weight, grip strength, and muscle cross-sectional area.
- Muscle-localized neutrophils increased significantly post-sepsis, correlating with atrophy severity.
- Neutrophil depletion reversed sepsis-induced muscle atrophy and grip strength deficits.
Conclusions:
- Sepsis leads to neutrophil infiltration in muscles, causing atrophy and weakness.
- Neutrophils play a critical role in the development of sepsis-induced muscle atrophy and weakness.
- Targeting neutrophils may offer therapeutic potential for sepsis-related muscle dysfunction.

