1. Department of Spinal Surgery, The University of Hong Kong-Shenzhen Hospital,Guangdong,Shenzhen,China,518000
2. Department of Orthopedics and Traumatology, Li Ka Shing Faculty of Medicine, The University of Hong Kong,Hong Kong SAR,China,999077
3. College of Life Sciences, University of Chinese Academy of Sciences,Beijing,China,100000
4. Lars Bolund Institute of Regenerative Medicine, Qingdao-Europe Advanced Institute for Life Sciences, BGI-, Qingdao,Shandong,Qingdao,China,266000
5. Department of Plastic and Reconstructive Surgery, Xijing Hospital, Forth Military Medical University,Shaanxi,Xi'an,China,710000
6. China Medical University,Liaoning,Shenyang,China,110000
Published:2023,
Published Online:1 November 2023,
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Xin Qiu, Hao-Yu Wang, Zhen-Yu Yang, et al. Uncovering the prominent role of satellite cells in paravertebral muscle development and aging by single-nucleus RNA sequencing. [J]. Genes & Diseases 1(6):2597-2613(2023)
Xin Qiu, Hao-Yu Wang, Zhen-Yu Yang, et al. Uncovering the prominent role of satellite cells in paravertebral muscle development and aging by single-nucleus RNA sequencing. [J]. Genes & Diseases 1(6):2597-2613(2023) DOI: 10.1016/j.gendis.2023.01.005.
To uncover the role of satellite cells (SCs) in paravertebral muscle development and aging
we constructed a single-nucleus transcriptomic atlas of mouse paravertebral muscle across seven timepoints spanning the embryo (day 16.5) to old (month 24) stages. Eight cell types
including SCs
fast muscle cells
and slow muscle cells
were identified. An energy metabolism-related gene set
TCA CYCLE IN SENESCENCE
was enriched in SCs. Forty-two skeletal muscle disease-related genes were highly expressed in SCs and exhibited similar expression patterns. Among them
Pdha1
was the core gene in the TCA CYCLE IN SENESCENCE;
Pgam2
Sod1
and
Suclg1
are transcription factors closely associated with skeletal muscle energy metabolism. Transcription factor enrichment analysis of the 42 genes revealed that
Myod1
and
Mef2a
were also highly expressed in SCs
which regulated
Pdha1
expression and were associated with skeletal muscle development. These findings hint that energy metabolism may be pivotal in SCs development and aging. Three ligand-receptor pairs of extracellular matrix (ECM)-receptor interactions
Lamc1
-
Dag1
Lama2
-
Dag1
and
Hspg2
-
Dag1
may play a vital role in SCs interactions with slow/fast muscle cells and SCs self-renewal. Finally
we built the first database of a skeletal muscle single-cell transcriptome
the Musculoskeletal Cell Atlas (http://www.mskca.tech)
which lists 630
040 skeletal muscle cells and provides interactive visualization
a useful resource for revealing skeletal muscle cellular heterogeneity during development and aging. Our study could provide new targets and ideas for developing drugs to inhibit skeletal muscle aging and treat skeletal muscle diseases.
NicheParaspinal muscleSatellite cellsSenescenceSingle-nucleus RNA sequencing
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