4.7 Article

3D-printed Sr2ZnSi2O7 scaffold facilitates vascularized bone regeneration through macrophage immunomodulation

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fbioe.2022.1007535

Keywords

3D printing; immunomodulation; osteogenesis; angiogenesis; bone defect

Funding

  1. National Natural Science Foundation of China [31900945, 81873949]
  2. Zhejiang Traditional Chinese Medicine Scientific Research Fund Project [2022ZB342]
  3. Zhejiang Province Medical and Health Science and Technology Project [2022512117]
  4. Major Science and Technology Project of Wenzhou Science and Technology Bureau [2018ZY002]
  5. Wenzhou Institute, University of Chinese Academy of Sciences [WIUCASQD2020013, WIUCASQD2021030]

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Biomaterial-based bone grafts have been shown to be effective in treating large bone defects, and this study highlights the importance of immunomodulation and immune-regulated bone regeneration in addition to the direct interaction between scaffolds and bone-related cells. The study presents a three-dimensional printed silicate bioceramic scaffold with well-defined pore structures, which has the potential to be an implantable biomaterial for bone repair.
Biomaterial-based bone grafts are emerged as an effective strategy for the treatment of large bone defects, especially for the scaffolds with enhanced osteogenic and angiogenic bioactivities. However, most studies focused on the direct interactions between scaffolds and bone-related cells such as osteoblasts and endothelial cells, and ignored the effects of material-triggered immunomodulation and the subsequent immune-regulated bone regeneration process. In this study, we developed a silicate bioceramic (Sr2ZnSi2O7, SZS) scaffold with well-defined pore structures using a three-dimensional (3D) printing technique. The prepared scaffolds were biodegradable, and the released bioactive ions were beneficial for immunomodulation, which stimulated macrophages to release more pro-healing cytokines and less pro-inflammatory cytokines. The obtained scaffold/macrophage conditioned medium further promoted the proliferation and osteogenic differentiation of a murine preosteoblast cell line (MC3T3-E1), as well as the angiogenic activity of human umbilical vein endothelial cells (HUVECs). Moreover, the in vivo experiments of critical-sized calvarial defects in rats revealed that the 3D printed SZS scaffolds could facilitate more vascularized bone regeneration than the 3D printed beta-tricalcium phosphate (beta-TCP, a typical clinically used bioceramic) scaffolds, suggesting that the 3D-printed SZS scaffolds hold the potential as implantable biomaterials with favorable osteoimmunomodulation for bone repair.

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