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Fabrication of Vascularized DPSC Constructs for Efficient Pulp Regeneration.
Katata, C; Sasaki, J I; Li, A; Abe, G L; Nör, J E; Hayashi, M; Imazato, S.
Afiliación
  • Katata C; Department of Biomaterials Science, Osaka University Graduate School of Dentistry, Osaka, Japan.
  • Sasaki JI; Department of Restorative Dentistry and Endodontology, Osaka University Graduate School of Dentistry, Osaka, Japan.
  • Li A; Department of Biomaterials Science, Osaka University Graduate School of Dentistry, Osaka, Japan.
  • Abe GL; Department of Biomaterials Science, Osaka University Graduate School of Dentistry, Osaka, Japan.
  • Nör JE; Department of Biomaterials Science, Osaka University Graduate School of Dentistry, Osaka, Japan.
  • Hayashi M; Department of Cariology, Restorative Sciences and Endodontics, University of Michigan School of Dentistry, Ann Arbor, MI, USA.
  • Imazato S; Department of Restorative Dentistry and Endodontology, Osaka University Graduate School of Dentistry, Osaka, Japan.
J Dent Res ; 100(12): 1351-1358, 2021 11.
Article en En | MEDLINE | ID: mdl-33913364
ABSTRACT
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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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Células Madre / Pulpa Dental Tipo de estudio: Observational_studies Límite: Animals Idioma: En Revista: J Dent Res Año: 2021 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Células Madre / Pulpa Dental Tipo de estudio: Observational_studies Límite: Animals Idioma: En Revista: J Dent Res Año: 2021 Tipo del documento: Article País de afiliación: Japón