Pro-Inflammatory Mediation of Myoblast Proliferation

Skeletal muscle satellite cell function is largely dictated by the surrounding environment following injury. Immune cell infiltration dominates the extracellular space in the injured area, resulting in increased cytokine concentrations. While increased pro-inflammatory cytokine expression has been previously established in the first 3 days following injury, less is known about the time course of cytokine expression and the specific mechanisms of cytokine induced myoblast function. Therefore, the expression of IL-1 beta and IL-6 at several time points following injury, and their effects on myoblast proliferation, were examined. In order to do this, skeletal muscle was injured using barium chloride in mice and tissue was collected 1, 5, 10, and 28 days following injury. Mechanisms of cytokine induced proliferation were determined in cell culture using both primary and C2C12 myoblasts. It was found that there is a similar to 20-fold increase in IL-1 beta ( p <= 0.05) and IL-6 ( p = 0.06) expression 5 days following injury. IL-1b increased proliferation of both primary and C2C12 cells similar to 25%. IL-1 beta stimulation also resulted in increased NF-kappa B activity, likely contributing to the increased proliferation. These data demonstrate for the first time that IL-1 beta alone can increase the mitogenic activity of primary skeletal muscle satellite cells and offer insight into the mechanisms dictating satellite cell function following injury.