4.5 Article

In vitro and in vivo osteogenesis up-regulated by two-dimensional nanosheets through a macrophage-mediated pathway

Journal

BIOMATERIALS SCIENCE
Volume 9, Issue 3, Pages 780-794

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0bm01596b

Keywords

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Funding

  1. National Natural Science Foundation of China [81802138, 81670807, 81871822, 81801395, 81702237, 81701383, 81600699]
  2. Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences [2019-RC-HL-024]
  3. Science and Technology Plan Project of Hunan Province [2017XK2039, 2018RS3029]
  4. Innovation Driven Project of Central South University [2019CX014, 2018CX029]
  5. Natural Science Foundation of Hunan Province of China [2020JJ5883, 2020JJ5900]

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A novel calcium phosphate material with a 2D nanostructure was developed, showing enhancement of in vitro osteogenic differentiation through macrophage-mediated signal pathway. The encapsulated CaP nanomaterials in a gelatin hydrogel demonstrated the ability to mediate in vivo ossification via a macrophage polarization related pathway, suggesting a potential alternative for bone autograft in orthopedic applications.
Two-dimensional (2D) nanomaterials are attracting more and more interest in regenerative medicine due to their unique properties; however 2D biomimetic calcium mineral has not yet been developed and demonstrated application for bone tissue engineering. Here we described a novel calcium phosphate material with a 2D nanostructure that was synthesized using collagen and sodium alginate as the template. In vitro performance of the nanocrystalline material was evaluated, and we found that 2D CaP nanoparticles (NPs) enhanced the in vitro osteogenic differentiation of rat mesenchymal stem cells (rMSCs) through a macrophage-mediated signal pathway, when co-cultured with RAW 264.7 cells, rather than direct NP/stem cell interaction. A 2D topology structured surface was constructed by encapsulating the CaP nanomaterials in a gelatin hydrogel, which was demonstrated to be able to mediate in vivo ossification through a macrophage polarization related pathway in a femur defect rat model, and allowed the optimal therapeutic outcome compared to normal CaP counterparts. Our current work may have enlightened a new mechanism regarding NP-induced stem cell differentiation through immunoregulation, and the 2D CaP encapsulated hydrogel scaffold may serve as a potential alternative to autograft bone for orthopedic applications.

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