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Evaluation of the effect of 3D-bioprinted gingival fibroblast-encapsulated ADM scaffolds on keratinized gingival augmentation.
Liu, Peng; Li, Qing; Yang, Qiaolin; Zhang, Shihan; Yi, Ke; Zhang, Guifeng; Tang, Zhihui.
Afiliación
  • Liu P; Second Clinical Division, Peking University School and Hospital of Stomatology, Beijing, 100101, P. R. China.
  • Li Q; Center of Digital Dentistry, Peking University School and Hospital of Stomatology, Beijing, 100081, P. R. China.
  • Yang Q; National Center of Stomatology and National Clinical Research Center for Oral Diseases and National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, Beijing, 100081, P. R. China.
  • Zhang S; Second Clinical Division, Peking University School and Hospital of Stomatology, Beijing, 100101, P. R. China.
  • Yi K; Center of Digital Dentistry, Peking University School and Hospital of Stomatology, Beijing, 100081, P. R. China.
  • Zhang G; National Center of Stomatology and National Clinical Research Center for Oral Diseases and National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, Beijing, 100081, P. R. China.
  • Tang Z; National Center of Stomatology and National Clinical Research Center for Oral Diseases and National Engineering Research Center of Oral Biomaterials and Digital Medical Devices, Beijing, 100081, P. R. China.
J Periodontal Res ; 58(3): 564-574, 2023 Jun.
Article en En | MEDLINE | ID: mdl-37042165
ABSTRACT
BACKGROUND AND

OBJECTIVES:

The keratinized gingiva plays an important role in maintaining healthy periodontal and peri-implant tissue. Acellular dermal matrix (ADM), as a substitute biomaterial, has a porous structure and good biocompatibility. 3D-bioprinting has the potential for tissue engineering because it enables precise loading of cells layer-by-layer. Herein, we bioprinted ADM scaffold encapsulating gingival fibroblasts (GFs) and evaluated its efficacy in keratinized gingiva augmentation in vivo to assess its potential for clinical periodontal tissue regeneration.

METHODS:

GFs were extracted from the gingiva of beagles and transfected with a green fluorescent protein (GFP). The ADM scaffold (ADM cell-free group) was constructed using ADM, gelatin, and sodium alginate mixed at an appropriate ratio via 3D-bioprinting. The ADM cell scaffold (ADM cell group) was established by adding extra GFs in the same manner. Six beagles were divided into blank control, ADM cell-free, and ADM cell groups; and implant surgery was performed. The keratinized gingiva was clinically and histologically evaluated at baseline and after 2 months.

RESULTS:

GFs transfected with GFPs expressed green fluorescence and were present in new tissue in the ADM cell group and not observed in the ADM cell-free group. At 2 months after surgery, the keratinized gingival augmentation in the ADM cell group was significantly more than that in the ADM cell-free group. Attached gingival augmentation was also observed more in the ADM cell group than that in the ADM cell-free group. Histological staining showed that the tissue in the ADM cell group displayed a more integrated structure and higher expression of COL I, COL III, and VEGF-A than those in the ADM cell-free group.

CONCLUSION:

3D-bioprinted GF-encapsulated ADM scaffolds increased the amount of keratinized gingiva in vivo, suggesting that 3D-bioprinting has great potential for oral soft tissue regeneration.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dermis Acelular / Recesión Gingival Límite: Animals Idioma: En Revista: J Periodontal Res Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dermis Acelular / Recesión Gingival Límite: Animals Idioma: En Revista: J Periodontal Res Año: 2023 Tipo del documento: Article