A pH-Triggered, Self-Assembled, and Bioprintable Hybrid Hydrogel Scaffold for Mesenchymal Stem Cell Based Bone Tissue Engineering
Author(s) -
Zhao Chen,
Nader Taheri Qazvini,
Monirosadat Sadati,
Zongyue Zeng,
Shifeng Huang,
Ana Losada de la Lastra,
Linghuan Zhang,
Yixiao Feng,
Wei Liu,
Bo Huang,
Bo Zhang,
Zhengyu Dai,
Yi Shen,
Xi Wang,
Wenping Luo,
Bo Liu,
Yan Lei,
Zhenyu Ye,
Ling Zhao,
Daigui Cao,
Lijuan Yang,
Xian Chen,
Aravind Athiviraham,
Michael J. Lee,
Jennifer Moriatis Wolf,
Russell R. Reid,
Matthew Tirrell,
Wei Huang,
Juan Pablo,
TongChuan He
Publication year - 2019
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.8b19094
Subject(s) - mesenchymal stem cell , materials science , scaffold , tissue engineering , biomedical engineering , biocompatibility , bone tissue , regeneration (biology) , microbiology and biotechnology , medicine , biology , metallurgy
Effective bone tissue engineering can restore bone and skeletal functions that are impaired by traumas and/or certain medical conditions. Bone is a complex tissue and functions through orchestrated interactions between cells, biomechanical forces, and biofactors. To identify ideal scaffold materials for effective mesenchymal stem cell (MSC)-based bone tissue regeneration, here we develop and characterize a composite nanoparticle hydrogel by combining carboxymethyl chitosan (CMCh) and amorphous calcium phosphate (ACP) (designated as CMCh-ACP hydrogel). We demonstrate that the CMCh-ACP hydrogel is readily prepared by incorporating glucono δ-lactone (GDL) into an aqueous dispersion or rehydrating the acidic freeze-dried nanoparticles in a pH-triggered controlled-assembly fashion. The CMCh-ACP hydrogel exhibits excellent biocompatibility and effectively supports MSC proliferation and cell adhesion. Moreover, while augmenting BMP9-induced osteogenic differentiation, the CMCh-ACP hydrogel itself is osteoinductive and induces the expression of osteoblastic regulators and bone markers in MSCs in vitro. The CMCh-ACP scaffold markedly enhances the efficiency and maturity of BMP9-induced bone formation in vivo, while suppressing bone resorption occurred in long-term ectopic osteogenesis. Thus, these results suggest that the pH-responsive self-assembled CMCh-ACP injectable and bioprintable hydrogel may be further exploited as a novel scaffold for osteoprogenitor-cell-based bone tissue regeneration.
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