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Translation of remote control regenerative technologies for bone repair

Markides, Hareklea; McLaren, Jane S.; Telling, Neil D.; Alom, Noura; Al-Mutheffer, E’atelaf A.; Oreffo, Richard; Zannettino, Andrew; Scammell, Brigitte E.; White, Lisa J.; El-Haj, Alicia

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Authors

Hareklea Markides

JANE MCLAREN jane.mclaren@nottingham.ac.uk
Nottingham Senior Tissue Bank Manager

Neil D. Telling

Noura Alom

E’atelaf A. Al-Mutheffer

Richard Oreffo

Andrew Zannettino

Brigitte E. Scammell

Alicia El-Haj



Abstract

The role of biomechanical stimuli, or mechanotransduction, in normal bone homeostasis and repair is understood to facilitate effective osteogenesis of mesenchymal stem cells (MSCs) in vitro. Mechanotransduction has been integrated into a multitude of in vitro bone tissue engineering strategies and provides an effective means of controlling cell behaviour towards therapeutic outcomes. However, the delivery of mechanical stimuli to exogenous MSC populations, post implantation, poses a significant translational hurdle. Here, we describe an innovative bio-magnetic strategy, MICA, where magnetic nanoparticles (MNPs) are used to remotely deliver mechanical stimuli to the mechano-receptor, TREK-1, resulting in activation and downstream signalling via an external magnetic array. In these studies, we have translated MICA to a pre-clinical ovine model of bone injury to evaluate functional bone repair. We describe the development of a magnetic array capable of in vivo MNP manipulation and subsequent osteogenesis at equivalent field strengths in vitro. We further demonstrate that the viability of MICA-activated MSCs in vivo is unaffected 48 hrs post implantation. We present evidence to support early accelerated repair and preliminary enhanced bone growth in MICA-activated defects within individuals compared to internal controls. The variability in donor responses to MICA-activation was evaluated in vitro revealing that donors with poor osteogenic potential were most improved by MICA-activation. Our results demonstrate a clear relationship between responders to MICA in vitro and in vivo. These unique experiments offer exciting clinical applications for cell-based therapies as a practical in vivo source of dynamic loading, in real-time, in the absence of pharmacological agents.

Citation

Markides, H., McLaren, J. S., Telling, N. D., Alom, N., Al-Mutheffer, E. A., Oreffo, R., Zannettino, A., Scammell, B. E., White, L. J., & El-Haj, A. (2018). Translation of remote control regenerative technologies for bone repair. npj Regenerative Medicine, 3(9), 1-12. https://doi.org/10.1038/s41536-018-0048-1

Journal Article Type Article
Acceptance Date Feb 20, 2018
Online Publication Date Apr 17, 2018
Publication Date Apr 17, 2018
Deposit Date Feb 23, 2018
Publicly Available Date Mar 30, 2020
Journal npj Regenerative Medicine
Electronic ISSN 2057-3995
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 3
Issue 9
Pages 1-12
DOI https://doi.org/10.1038/s41536-018-0048-1
Keywords Magnetic nanoparticles, bone repair, pre-clinical ovine models, cell therapy, mechanotransduction, clinical translation
Public URL https://nottingham-repository.worktribe.com/output/926214
Publisher URL https://www.nature.com/articles/s41536-018-0048-1

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