Transcriptional profiling of quiescent muscle stem cells in vivo
Open accessAbstract
Muscle stem cells (MuSCs) persist in a quiescent state and activate in response to specific stimuli. The quiescent state is both actively maintained and dynamically regulated. However, analyses of quiescence have come primarily from cells removed from their niche. Although these cells are still quiescent, biochemical changes certainly occur during the isolation process. Here, we analyze the transcriptome of MuSCs in vivo utilizing MuSC-specific labeling of RNA. Notably, labeling transcripts during the isolation procedure revealed very active transcription of specific subsets of genes. However, using the transcription inhibitor α-amanitin, we show that the ex vivo transcriptome remains largely reflective of the in vivo transcriptome. Together, these data provide perspective on the molecular regulation of the quiescent state at the transcriptional level, demonstrate the utility of these tools for probing transcriptional dynamics in vivo, and provide an invaluable resource for understanding stem cell state transitions.
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FACS-isolated cells used here express some markers of early MuSC activation, even immediately after isolation.
“Recent studies have reported that the FACS-isolated cells used here express some markers of early MuSC activation, even immediately after isolation. Therefore, our ‘quiescent’ cell populations probably experience some early activation stimulus during isolation (Machado et al., 2017; Velthoven et al., 2017).”
From Aging induces aberrant state transition kinetics in murine muscle stem cells (2020) · cites this paper as Velthoven et al., 2017
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References 38 · Cited by 235
- Authors
- van Velthoven, C. T. J., de Morree, A., Egner, I. M., Brett, J. O., & Rando, T. A.
- Affiliations
- University of Oslo (NO)
- Stanford Medicine (US)
- VA Palo Alto Health Care System (US)
- Corresponding author
- Rando, Thomas A.
- Venue
- Cell Reports
- Publisher
- Elsevier BV
- Published
- 2017-11
- Volume
- 21
- Issue
- 7
- Pages
- 1994-2004
- ISSN
- 2211-1247 (ISSN-L)
- PMC
- PMC5711481
- OpenAlex
- W2769123411
- Cited by
- 235
- References
- 38
- Citations by year
- 2026: 15 · 2025: 18 · 2024: 24 · 2023: 22 · 2022: 32 · 2021: 46 · 2020: 34 · 2019: 18 · 2018: 24 · 2017: 1
- FWCI
- 8.60
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Cell Reports (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- NORA - Norwegian Open Research Archives (submittedVersion, cc-by-nc-nd)
- Funders
- Glenn Foundation for Aging Research
- Muscular Dystrophy Association
- NIH (P01 AG036695, R01 AG23806, R01 AG047820)
- California Institute of Regenerative Medicine
- Department of Veterans Affairs
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Keywords
- muscle stem cells, quiescence, gene expression profiling, RNA labeling, alpha-amanitin, stem cell niche, gene expression regulation
- MeSH terms
- Animals, Male, Mice, Inbred C57BL, Gene Expression Profiling, Myoblasts, Mice, Transcriptome
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