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Updated: May 29, 2026

Treatment of Ligament Constructs with Exercise-conditioned Serum: A Translational Tissue Engineering Model
Published on: June 11, 2017
Androgens affect myogenesis in vitro and increase local IGF-1 expression.
Nick Sculthorpe1, Andrew M Solomon, Andrea C M Sinanan
1Muscle Cellular and Molecular Physiology Research Group, Institute for Sport and Physical Activity Research, University of Bedfordshire, Bedford, United Kingdom. nick.sculthorpe@beds.ac.uk
Anabolic androgens like testosterone (T) and insulin-like growth factor 1 (IGF-1) promote skeletal muscle growth. T increases IGF-1 messenger RNA (mRNA) production, suggesting IGF-1 mediates androgen effects on muscle hypertrophy.
Area of Science:
- Molecular Endocrinology
- Cellular Biology
- Muscle Physiology
Background:
- The precise mechanisms linking anabolic androgens to skeletal muscle hypertrophy are not fully elucidated.
- A potential interaction between androgens and locally produced insulin-like growth factor 1 (IGF-1) is hypothesized to play a role in muscle growth.
- Understanding these pathways is crucial for developing therapeutic strategies for muscle wasting conditions.
Purpose of the Study:
- To investigate whether androgens enhance the differentiation of human muscle precursor cells in vitro.
- To examine the effects of testosterone (T) alone and in combination with IGF-1 on IGF-1 messenger RNA (mRNA) expression.
- To elucidate the role of IGF-1 as a mediator in androgen-induced muscle hypertrophy.
Main Methods:
- Human muscle-derived cells were cultured under low-serum conditions to induce differentiation.
- Cultures were exposed to varying concentrations of testosterone (T) or IGF-1 for 3 or 7 days.
- Immunocytochemistry and real-time polymerase chain reaction (RT-PCR) were employed to assess myogenic commitment, fusion index, and gene expression, including androgen receptor levels.
Main Results:
- After 7 days of exposure, both T and IGF-1 significantly increased the muscle cell fusion index, indicating enhanced differentiation.
- Testosterone (T) treatment led to a significant increase in IGF-1 mRNA expression, while exogenous IGF-1 reduced IGF-1 mRNA transcription.
- The observed effects of T on muscle differentiation were reversible upon treatment with flutamide, an androgen receptor antagonist.
Conclusions:
- Both testosterone (T) and insulin-like growth factor 1 (IGF-1) promote myogenic commitment in human muscle precursor cells after prolonged exposure.
- Testosterone (T) upregulates IGF-1 mRNA, supporting the role of IGF-1 as a key mediator in androgen-driven cellular pathways for muscle hypertrophy.
- This study establishes a novel in vitro model for investigating growth factor involvement in androgen-mediated skeletal muscle development.
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