4.8 Article

A novel Lipidoid-MicroRNA formulation promotes calvarial bone regeneration

Journal

BIOMATERIALS
Volume 177, Issue -, Pages 88-97

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2018.05.038

Keywords

Lipidoid; microRNA; miR-335-5p; Bone marrow stromal cells (BMSCs); Osteogenic differentiation; Bone formation

Funding

  1. National Institutes of Health, United States [R01DE021464, R01DE025681]
  2. Innovation in Oral Care Award through International Association for Dental Research, United States
  3. GlaxoSmithKline Consumer Healthcare, United Kingdom
  4. International Team of Implantology, Switzerland

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Specific microRNAs (miRs) and the Wnt signaling pathway play critical roles in regulating bone development and homeostasis. Our previous studies revealed the ability of miR-335-5p to promote osteogenic differentiation by down regulating Wnt antagonist Dickkopf-1 (DKK1). The purpose of this study was to use nano-materials to efficiently deliver miR-335-5p into osteogenic cells for tissue engineering applications. We synthesized and screened a library of 12 candidate nano-lipidoids , of which L8 was identified as the preferred biodegradable lipidoid for miRNA molecule delivery into cells. We then investigated whether a lipidoid-miRNA formulation of miR-335-5-p (LMF-335) could successfully deliver miR-335-5-p into cells to promote osteogenesis in vitro and calvarial bone healing in vivo. Transfection of C3H10T1/2 cells and bone marrow stromal cells (BMSCs) with LMF-335 led to decreased expression of DKK1 and increased expression of the key osteogenic genes. LMF-335 and LMF-335-transfected BMSCs were then used in combination with silk scaffolds to evaluate healing of critical-size calvarial bone defects in mice. The results revealed significant new bone formation in the defects in LMF-335 groups as compared with control groups. In conclusion, this first report supports the notion that lipidoid delivery of miRNA can be used to induce osteogenic differentiation of stem cells and bone regeneration. (C) 2018 Elsevier Ltd. All rights reserved.

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