Secretoglobin 3A1 in activated muscle satellite cells contributes to myosin heavy chain IIX and IIB fiber differentiation

Skeletal muscle has an innate ability to restore damaged muscle fibers by contributing specific progenitor cells, called muscle satellite cells. Here we show that secretoglobin (SCGB) 3A1, a tumor suppressor gene in various malignancies including rhabdomyosarcoma, is induced just after muscle injury and contributes to damaged muscle fiber regeneration. Lineage tracing of SCGB3A1 in mice show that SCGB3A1-positive cells highly express myosin heavy chain (MyHC)-IIX in damaged fiber area. Scgb3a1-null and Pax7<sup>CreERT2</sup>;Scgb3a1<sup>f/f</sup> conditional-null mice exhibit defective IIX and IIB fiber regeneration, with a concomitant reduction in the expression of Notch3, a gene important for the maintenance of satellite cell self-renewal pools. Aged Scgb3a1-null mice show reduced size of muscle fibers and mass, resulting in compromised muscle performance as compared to the age-matched wild-type mice. This study reveals that SCGB3A1 is an unexpected novel molecule expressed in muscle satellite cells that contributes to fiber type specific muscle regeneration.

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Publication Details

Journal
Cellular and Molecular Life Sciences
Published
2025-12-31
DOI
https://doi.org/10.1007/s00018-025-06045-5
Primary Topic
Muscle Physiology and Disorders
Type
article
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article

Secretoglobin 3A1 in activated muscle satellite cells contributes to myosin heavy chain IIX and IIB fiber differentiation

Mitsuhiro Yoneda, Parirokh P. Awasthi, Shioko Kimura, Danielle Springer et al.
Cellular and Molecular Life Sciences
Muscle Physiology and Disorders
article

Secretoglobin 3A1 in activated muscle satellite cells contributes to myosin heavy chain IIX and IIB fiber differentiation

Mitsuhiro Yoneda, Parirokh P. Awasthi, Shioko Kimura, Danielle Springer, Andrew D. Patterson, Shigetoshi Yokoyama, Raj Chari, Taketomo Kido
article en

Abstract

Skeletal muscle has an innate ability to restore damaged muscle fibers by contributing specific progenitor cells, called muscle satellite cells. Here we show that secretoglobin (SCGB) 3A1, a tumor suppressor gene in various malignancies including rhabdomyosarcoma, is induced just after muscle injury and contributes to damaged muscle fiber regeneration. Lineage tracing of SCGB3A1 in mice show that SCGB3A1-positive cells highly express myosin heavy chain (MyHC)-IIX in damaged fiber area. Scgb3a1-null and Pax7<sup>CreERT2</sup>;Scgb3a1<sup>f/f</sup> conditional-null mice exhibit defective IIX and IIB fiber regeneration, with a concomitant reduction in the expression of Notch3, a gene important for the maintenance of satellite cell self-renewal pools. Aged Scgb3a1-null mice show reduced size of muscle fibers and mass, resulting in compromised muscle performance as compared to the age-matched wild-type mice. This study reveals that SCGB3A1 is an unexpected novel molecule expressed in muscle satellite cells that contributes to fiber type specific muscle regeneration.

Cellular and Molecular Life SciencesVol. 83(1)
Pennsylvania State University (US), Quantitative BioSciences (US), National Heart, Lung, and Blood Institute (US), Frederick National Laboratory for Cancer Research (US), National Cancer Institute (US), Nagasaki University (JP)
Openalex Percentile: Top 35%
Muscle Physiology and Disorders
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