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Updated: Feb 2, 2026

Quantifying Subcellular Ubiquitin-proteasome Activity in the Rodent Brain
Published on: May 21, 2019
The Ubiquitin-Proteasome System Is Indispensable for the Maintenance of Muscle Stem Cells
Yasuo Kitajima1, Naoki Suzuki2, Aki Nunomiya3
1Musculoskeletal Molecular Biology Research Group, Nagasaki University Graduate School of Biomedical Sciences, Basic and Translational Research Center for Hard Tissue Disease, 1-7-1 Sakamoto, Sakamoto, Nagasaki 852-8588, Japan; Japan Society for the Promotion of Science, Tokyo, Japan.
Abstract:
Adult muscle stem cells (satellite cells) are required for adult skeletal muscle regeneration. A proper balance between quiescence, proliferation, and differentiation is essential for the maintenance of the satellite cell pool and their regenerative function. Although the ubiquitin-proteasome is required for most protein degradation in mammalian cells, how its dysfunction affects tissue stem cells remains unclear. Here, we investigated the function of the proteasome in satellite cells using mice lacking the crucial proteasomal component, Rpt3. Ablation of Rpt3 in satellite cells decreased proteasome activity. Proteasome dysfunction in Rpt3-deficient satellite cells impaired their ability to proliferate, survive and differentiate, resulting in defective muscle regeneration. We found that inactivation of proteasomal activity induced proliferation defects and apoptosis in satellite cells. Mechanistically, insufficient proteasomal activity upregulated the p53 pathway, which caused cell-cycle arrest. Our findings delineate a critical function of the proteasome system in maintaining satellite cells in adult muscle.
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