4.7 Article

Fabrication of Vascularized DPSC Constructs for Efficient Pulp Regeneration

期刊

JOURNAL OF DENTAL RESEARCH
卷 100, 期 12, 页码 1351-1358

出版社

SAGE PUBLICATIONS INC
DOI: 10.1177/00220345211007427

关键词

tissue engineering; biomaterials; vascular endothelial cells; cell differentiation; endodontics; regenerative medicine

资金

  1. Japan Society for the Promotion of Science [17K11778, 17H04383]
  2. Grants-in-Aid for Scientific Research [17H04383, 17K11778] Funding Source: KAKEN

向作者/读者索取更多资源

Vascularized DPSC constructs, formed by inducing endothelial differentiation, showed enhanced blood supply and pulp regeneration when transplanted into human pulpless teeth, compared to DPSC constructs without prevascularization. This study demonstrates the potential of vascularized DPSC constructs as a biomaterial for novel dental pulp regeneration.
Dental pulp regeneration is a promising approach to restore the vitality of necrotic teeth. We have previously reported the fabrication of scaffold-free cell constructs containing only dental pulp stem cells (DPSCs) and their ability to form pulp-like tissue in the pulpless tooth. However, the DPSC construct could not build pulp-like tissue with a full root length because it is difficult to induce blood vessels from a small root canal foramen. Therefore, we hypothesized that vascular structure could be preformed in the DPSC construct by employing endothelial differentiation capability of DPSCs, and vascularized constructs might facilitate dental pulp regeneration in the pulpless tooth. In this study, vascularized DPSC constructs were fabricated by inducing endothelial differentiation, and then we investigated the behavior of differentiated DPSCs, the internal structure of cell constructs, and their pulp regenerative ability in vivo. We observed that DPSCs positive for CD31 and von Willebrand factor were localized at the outer layer of constructs and formed a reticulated lumen structure. The cells constituting the outer layer of the construct expressed endothelial differentiation markers at higher levels than cells in the inner part. These results indicated that DPSCs in the outer layer differentiated into endothelial cells and formed vascular-like structures in the cell construct. Next, a vascularized DPSC construct was transplanted into the human pulpless tooth that was implanted into immunodeficient mice in the subcutaneous space. After 6 wk of implantation, the vascularized construct formed pulp-like tissues with higher density of human CD31-positive blood vessels when compared with specimens implanted with a DPSC construct without prevascularization. These results suggest that the vascular structure formed in the DPSC construct facilitated the blood supply and enhanced pulp regeneration. This study demonstrates that a vascularized DPSC construct is a prospective biomaterial as an implant for novel dental pulp regeneration.

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