1. Academic Validation
  2. Osteoinductive Dental Pulp Stem Cell-Derived Extracellular Vesicle-Loaded Multifunctional Hydrogel for Bone Regeneration

Osteoinductive Dental Pulp Stem Cell-Derived Extracellular Vesicle-Loaded Multifunctional Hydrogel for Bone Regeneration

  • ACS Nano. 2024 Mar 15. doi: 10.1021/acsnano.3c11542.
Li Wang 1 Xinbo Wei 1 Xi He 1 Shengzhao Xiao 1 2 Qiusheng Shi 1 Peng Chen 3 Jesse Lee 4 Ximin Guo 5 Haifeng Liu 1 Yubo Fan 1
Affiliations

Affiliations

  • 1 Key Laboratory for Biomechanics and Mechanobiology (Beihang University) of Ministry of Education, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University, Beijing 100083, P.R. China.
  • 2 Department of Orthodontics, Shanghai Ninth People's Hospital, College of Stomatology, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, P.R. China.
  • 3 Department of Ultrasound, The Third Medical Center, Chinese PLA General Hospital, Beijing 100039, P.R. China.
  • 4 Arova Biosciences, Inc., Life Sciences Innovation Hub, Calgary Alberta T2L 1Y8, Canada.
  • 5 Department of Advanced Interdisciplinary Studies, Institute of Basic Medical Sciences, Beijing 100850, P.R. China.
Abstract

Stem cell-derived extracellular vesicles (EVs) show great potential for promoting bone tissue regeneration. However, normal EVs (Nor-EVs) have a limited ability to direct tissue-specific regeneration. Therefore, it is necessary to optimize the osteogenic capacity of EV-based systems for repairing extensive bone defects. Herein, we show that hydrogels loaded with osteoinductive dental pulp stem cell-derived EVs (Ost-EVs) enhanced bone tissue remodeling, resulting in a 2.23 ± 0.25-fold increase in the expression of Bone Morphogenetic Protein 2 (BMP2) compared to the hydrogel control group. Moreover, Ost-EVs led to a higher expression of Alkaline Phosphatase (ALP) (1.88 ± 0.16 of Ost-EVs relative to Nor-EVs) and the formation of orange-red calcium nodules (1.38 ± 0.10 of Ost-EVs relative to Nor-EVs) in vitro. RNA sequencing revealed that Ost-EVs showed significantly high miR-1246 expression. An ideal hydrogel implant should also adhere to surrounding moist tissues. In this study, we were drawn to mussel-inspired adhesive modification, where the hydrogel carrier was crafted from hyaluronic acid (HA) and polyethylene glycol derivatives, showcasing impressive tissue adhesion, self-healing capabilities, and the ability to promote bone growth. The modified HA (mHA) hydrogel was also responsive to environmental stimuli, making it an effective carrier for delivering EVs. In an ectopic osteogenesis animal model, the Ost-EV/hydrogel system effectively alleviated inflammation, accelerated revascularization, and promoted tissue mineralization. We further used a rat femoral condyle defect model to evaluate the in situ osteogenic ability of the Ost-EVs/hydrogel system. Collectively, our results suggest that Ost-EVs combined with biomaterial-based hydrogels hold promising potential for treating bone defects.

Keywords

Schiff’s base reaction; bone tissue engineering; dental pulp stem cells; engineered extracellular vesicles; hyaluronic acid hydrogel.

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