JOSEPH BASS Joseph.Bass@nottingham.ac.uk
Assistant Professor (Physiology and Endocrionolgy)
Overexpression of the vitamin D receptor (VDR) induces skeletal muscle hypertrophy
Authors
Asif Nakhuda
Colleen S. Deane
MATTHEW BROOK MATTHEW.BROOK@NOTTINGHAM.AC.UK
Assistant Professor
DANIEL WILKINSON DANIEL.WILKINSON@NOTTINGHAM.AC.UK
Assistant Professor
BETH PHILLIPS beth.phillips@nottingham.ac.uk
Professor of Translational Physiology
Andrew Philp
Janelle Tarum
Fawzi Kadi
Ditte Andersen
Garcia
Ken Smith
Iain J. Gallagher
Nathaniel J. Szewczyk
Mark E. Cleasby
PHILIP ATHERTON philip.atherton@nottingham.ac.uk
Professor of Clinical, metabolic & Molecular Physiology
Abstract
Objective
The Vitamin D receptor (VDR) has been positively associated with skeletal muscle mass, function and regeneration. Mechanistic studies have focused upon loss of the receptor, with in vivo whole-body knockout models demonstrating reduced myofiber size and function, and impaired muscle development. To understand the mechanistic role upregulation of the VDR elicits in muscle mass/health, we studied the impact of VDR over-expression (OE) in vivo, before exploring the importance of VDR expression upon muscle hypertrophy in humans.
Methods
Wistar rats underwent in vivo electrotransfer (IVE) to over-express the VDR in Tibialis anterior (TA) muscle for 10 days, before comprehensive physiological and metabolic profiling to characterise the influence of VDR-OE on muscle protein synthesis (MPS), anabolic signalling and satellite cell activity. Stable isotope tracer (D2O) techniques were used to assess sub-fraction protein synthesis, alongside RNA-Seq analysis. Finally, human participants underwent 20-wks resistance exercise training, with body composition and transcriptomic analysis.
Results
Muscle VDR-OE yielded total protein and RNA accretion, manifesting in increased myofibre area i.e. hypertrophy. The observed increases in MPS were associated with enhanced anabolic signalling reflecting translational efficiency (e.g. mTOR-signalling), with no effects upon protein breakdown markers being observed. Additionally, RNA-Seq illustrated marked extracellular matrix (ECM) remodeling, while satellite cell content, markers of proliferation and associated cell-cycled related gene-sets were up-regulated. Finally, induction of VDR mRNA correlated with muscle hypertrophy in humans following long-term resistance exercise type training.
Conclusion
VDR-OE stimulates muscle hypertrophy ostensibly via heightened protein synthesis, translational efficiency, ribosomal expansion and up-regulation of ECM remodelling related gene-sets. Furthermore, VDR expression is a robust marker of the hypertrophic response to resistance exercise in humans. The VDR is a viable target of muscle maintenance through testable Vitamin D molecules, as active molecules and analogs.
Citation
Bass, J. J., Nakhuda, A., Deane, C. S., Brook, M. S., Wilkinson, D. J., Phillips, B. E., …Atherton, P. J. (2020). Overexpression of the vitamin D receptor (VDR) induces skeletal muscle hypertrophy. Molecular Metabolism, 42, Article 101059. https://doi.org/10.1016/j.molmet.2020.101059
Journal Article Type | Article |
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Acceptance Date | Jul 28, 2020 |
Online Publication Date | Aug 7, 2020 |
Publication Date | Dec 1, 2020 |
Deposit Date | Aug 6, 2020 |
Publicly Available Date | Sep 9, 2020 |
Journal | Molecular Metabolism |
Electronic ISSN | 2212-8778 |
Publisher | Elsevier |
Peer Reviewed | Peer Reviewed |
Volume | 42 |
Article Number | 101059 |
DOI | https://doi.org/10.1016/j.molmet.2020.101059 |
Keywords | Vitamin D; Skeletal Muscle; Metabolism; Exercise |
Public URL | https://nottingham-repository.worktribe.com/output/4814467 |
Publisher URL | https://www.sciencedirect.com/science/article/pii/S2212877820301332 |
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