Regulation of Osteoimmune Microenvironment and Osteogenesis by 3D‐Printed PLAG/black Phosphorus Scaffolds for Bone Regeneration

Author:

Long Jing1ORCID,Yao Zhenyu1,Zhang Wei1,Liu Ben1,Chen Kaiming1,Li Long1,Teng Bin2,Du Xiang‐Fu1,Li Cairong1,Yu Xue‐Feng3,Qin Ling145ORCID,Lai Yuxiao1567ORCID

Affiliation:

1. Centre for Translational Medicine Research & Development Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen 518055 P. R. China

2. Center for Energy Metabolism and Reproduction Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen 518055 P. R. China

3. Materials and Interfaces Center Shenzhen Institute of Advanced Technology Chinese Academy of Sciences Shenzhen 518055 P. R. China

4. Musculoskeletal Research Laboratory Department of Orthopaedics & Traumatology The Chinese University of Hong Kong HK Hong Kong SAR 999077 P. R. China

5. CAS‐HK Joint Lab of Biomaterials Shenzhen 518055 P. R. China

6. Guangdong Engineering Laboratory of Biomaterials Additive Manufacturing Shenzhen 518055 P. R. China

7. Orthopaedics/Department of Spine Surgery the First Affiliated Hospital, Shenzhen University, Shenzhen Second People’s Hospital Shenzhen 518035 P. R. China

Abstract

AbstractThe treatment of bone defects remains a significant challenge to be solved clinically. Immunomodulatory properties of orthopedic biomaterials have significance in regulating osteoimmune microenvironment for osteogenesis. A lactic acid‐co‐glycolic acid (PLGA) scaffold incorporates black phosphorus (BP) fabricated by 3D printing technology to investigate the effect of BP on osteoimmunomodulation and osteogenesis in site. The PLGA/BP scaffold exhibits suitable biocompatibility, biodegradability, and mechanical properties as an excellent microenvironment to support new bone formation. The studies' result also demonstrate that the PLGA/BP scaffolds are able to recruit and stimulate macrophages M2 polarization, inhibit inflammation, and promote human bone marrow mesenchymal stem cells (hBMSCs) proliferation and differentiation, which in turn promotes bone regeneration in the distal femoral defect region of steroid‐associated osteonecrosis (SAON) rat model. Moreover, it is screened and demonstrated that PLGA/BP scaffolds can promote osteogenic differentiation by transcriptomic analysis, and PLGA/BP scaffolds promote osteogenic differentiation and mineralization by activating PI3K‐AKT signaling pathway in hBMSC cells. In this study, it is shown that the innovative PLGA/BP scaffolds are extremely effective in stimulating bone regeneration by regulating macrophage M2 polarization and a new strategy for the development of biomaterials that can be used to repair bone defects is offered.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

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