Abstract

Mesenchymal stem cells are increasingly studied for their use as drug‐carrier in addition to their intrinsic potential for regenerative medicine. They could be used to transport molecules with a poor bioavailability such as curcumin in order to improve their clinical usage. This natural polyphenol, well‐known for its antioxidant and anti‐inflammatory properties, has a poor solubility that limits its clinical potential. For this purpose, the use of NDS27, a curcumin salt complexed with hydroxypropyl‐beta‐cyclodextrin (HPβCD), displaying an increased solubility in aqueous solution, is preferred. This study aims to evaluate the uptake of NDS27 into skeletal muscle‐derived mesenchymal stem cells (mdMSCs) and the effects of such uptake onto their mesenchymal properties. It appeared that the uptake of NDS27 into mdMSCs is concentration‐dependent and not time‐dependent. The use of a concentration of 7 µmol/L which does not affect the viability and proliferation also allows preservation of their adhesion, invasion and T cell immunomodulatory abilities.

Highlights

  • Mesenchymal stem cells (MSCs) are multipotent stem cells implicated in homeostasis and tissue repair.[1]

  • This in vitro study was designed to evaluate the impact of NDS27 loading on equine muscle-­ derived MSCs (mdMSCs) in the aim to develop curcumin-­ loaded mdMSCs

  • This new therapeutic association would allow possibly benefiting from both mdMSCs regenerative therapy and curcumin effects to treat inflammatory diseases

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Summary

Introduction

Mesenchymal stem cells (MSCs) are multipotent stem cells implicated in homeostasis and tissue repair.[1]. This study aims to evaluate (a) the cellular toxicity of the NDS27 on MSCs, (b) the uptake and subcellular localization of NDS27 and (c) the effects of such loading (ie uptake) on mitochondrial function and mesenchymal properties of skeletal muscle-­ derived MSCs (mdMSCs)

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