Development of a multicellular 3D-bioprinted microtissue model of human periodontal ligament-alveolar bone biointerface: Towards a pre-clinical model of periodontal diseases and personalized periodontal tissue engineering

Vurat M. T., Şeker Ş., Lalegül Ülker Ö., Parmaksız M., Elçin A. E., Elçin Y. M.

GENES & DISEASES, cilt.9, sa.4, ss.1008-1023, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 9 Sayı: 4
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1016/j.gendis.2020.11.011
  • Dergi Adı: GENES & DISEASES
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED)
  • Sayfa Sayıları: ss.1008-1023
  • Anahtar Kelimeler: 3D bioprinting, Alveolar bone, Microtissue model, Organ-on-a-chip, Periodontal ligament, Periodontal tissue engineering, Periodontal-osteoblastic biointerface, Periodontium-on-a-chip, ON-A-CHIP, STEM-CELLS, IN-VITRO, GELATIN, HYDROXYAPATITE, TETRACYCLINES, FIBROBLASTS, HYDROGELS, DIFFERENTIATION, NANOPARTICLES
  • Ankara Üniversitesi Adresli: Evet

Özet

While periodontal (PD) disease is among principal causes of tooth loss worldwide, regulation of concomitant soft and mineralized PD tissues, and PD pathogenesis have not been completely clarified yet. Besides, relevant pre-clinical models and in vitro platforms have limitations in simulating human physiology. Here, we have harnessed three-dimensional bioprinting (3DBP) technology for developing a multi-cellular microtissue model resembling PD ligament-alveolar bone (PDL-AB) biointerface for the first time. 3DBP parameters were optimized; the physical, chemical, rheological, mechanical, and thermal properties of the constructs were assessed. Constructs containing gelatin methacryloyl (Gel-MA) and hydroxyapatite-magnetic iron oxide nanoparticles showed higher level of compressive strength when compared with that of Gel-MA constructs. Bioprinted self-supporting microtissue was cultured under flow in a microfluidic platform for >10 days without significant loss of shape fidelity. Confocal microscopy analysis indicated that encapsulated cells were homogenously distributed inside the matrix and preserved their viability for >7 days under microfluidic conditions. Immunofluorescence analysis showed the cohesion of stromal cell surface marker-1+