Proinflammatory Cytokine Tumor Necrosis Factor (TNF)-like Weak Inducer of Apoptosis (TWEAK) Suppresses Satellite Cell Self-renewal through Inversely Modulating Notch and NF-κB Signaling Pathways
Proinflammatory Cytokine Tumor Necrosis Factor (TNF)-like Weak Inducer of Apoptosis (TWEAK) Suppresses Satellite Cell Self-renewal through Inversely Modulating Notch and NF-κB Signaling Pathways
Satellite cell self-renewal is an essential process to maintaining the robustness of skeletal muscle regenerative capacity. However, extrinsic factors that regulate self-renewal of satellite cells are not well understood. Here, we demonstrate that TWEAK cytokine reduces the proportion of Pax7(+)/MyoD(-) cells (an index of self-renewal) on myofiber explants and represses multiple components of Notch signaling in satellite cell cultures. The number of Pax7(+) cells is significantly increased in skeletal muscle of TWEAK knock-out (KO) mice compared with wild-type in response to injury. Furthermore, Notch signaling is significantly elevated in cultured satellite cells and in regenerating myofibers of TWEAK-KO mice. Forced activation of Notch signaling through overexpression of the Notch1 intracellular domain (N1ICD) rescued the TWEAK-mediated inhibition of satellite cell self-renewal. TWEAK also activates the NF-κB transcription factor in satellite cells and inhibition of NF-κB significantly improved the number of Pax7(+) cells in TWEAK-treated cultures. Furthermore, our results demonstrate that a reciprocal interaction between NF-κB and Notch signaling governs the inhibitory effect of TWEAK on satellite cell self-renewal. Collectively, our study demonstrates that TWEAK suppresses satellite cell self-renewal through activating NF-κB and repressing Notch signaling.
- Purdue University West Lafayette United States
- University of Louisville United States
Mice, Knockout, Satellite Cells, Skeletal Muscle, NF-kappa B, PAX7 Transcription Factor, Apoptosis, Cytokine TWEAK, Recombinant Proteins, Protein Structure, Tertiary, Mice, Inbred C57BL, Mice, Tumor Necrosis Factors, Animals, Regeneration, Inflammation Mediators, Receptor, Notch1, Cells, Cultured, Cell Proliferation, MyoD Protein, Signal Transduction
Mice, Knockout, Satellite Cells, Skeletal Muscle, NF-kappa B, PAX7 Transcription Factor, Apoptosis, Cytokine TWEAK, Recombinant Proteins, Protein Structure, Tertiary, Mice, Inbred C57BL, Mice, Tumor Necrosis Factors, Animals, Regeneration, Inflammation Mediators, Receptor, Notch1, Cells, Cultured, Cell Proliferation, MyoD Protein, Signal Transduction
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