Mesenchymal stem cells surpass the capacity of bone marrow aspirate concentrate for periodontal regeneration

Autor(es)

Camila Alves Costa ^[1] ; Tatiana Miranda Deliberador ^[2] ; Rodrigo Paolo Flores Abuna ^[3] ; Thaisângela Lopes Rodrigues ^[4] ; Sérgio Luis Scombatti de Souza ^[5] ; Daniela Bazan Palioto ^[6]

Afiliação do(s) autor(es)

^[1] Universidade de São Paulo. Faculdade de Odontologia de Ribeirão Preto. Departamento de Cirurgia e Traumatologia Buco-Maxilo-Facial e Periodontia - Brasil

^[2] Universidade Positivo. Faculdade de Ciências da Saúde. Departamento de Odontologia - Brasil

^[3] Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Bioquímica e Imunologia - Brasil

^[4] Universidade Federal de Goiás. Faculdade de Farmácia. Laboratório de Farmacologia Celular e Toxicologia - Brasil

^[5] Universidade de São Paulo. Faculdade de Odontologia de Ribeirão Preto. Departamento de Cirurgia e Traumatologia Buco-Maxilo-Facial e Periodontia - Brasil

^[6] Universidade de São Paulo. Faculdade de Odontologia de Ribeirão Preto. Departamento de Cirurgia e Traumatologia Buco-Maxilo-Facial e Periodontia - Brasil

• Tipo de documento: Artigo Científico
• Fonte: Journal of Applied Oral Science; v. 30, 2022-04-01.

Resumo

Abstract Regenerative approaches using mesenchymal stem cells (MSCs) have been evaluated to promote the complete formation of all missing periodontal tissues, e.g., new cementum, bone, and functional periodontal ligaments. MSCs derived from bone marrow have been applied to bone and periodontal defects in several forms, including bone marrow aspirate concentrate (BMAC) and cultured and isolated bone marrow mesenchymal stem cells (BM-MSCs). This study aimed to evaluate the periodontal regeneration capacity of BMAC and cultured BM-MSCs in the wound healing of fenestration defects in rats. Methodology: BM-MSCs were obtained after bone marrow aspiration of the isogenic iliac crests of rats, followed by cultivation and isolation. Autogenous BMAC was collected and centrifuged immediately before surgery. In 36 rats, fenestration defects were created and treated with suspended BM-MSCs, BMAC or left to spontaneously heal (control) (N=6). Their regenerative potential was assessed by microcomputed tomography (µCT) and histomorphometry, as well as their cell phenotype and functionality by the Luminex assay at 15 and 30 postoperative days. Results: BMAC achieved higher bone volume in 30 days than spontaneous healing (p<0.0001) by enhancing osteoblastic lineage commitment maturation, with higher levels of osteopontin (p=0.0013). Defects filled with cultured BM-MSCs achieved higher mature bone formation in early stages than spontaneous healing and BMAC (p=0.0241 and p=0.0143, respectively). Moreover, significantly more cementum-like tissue formation (p<0.0001) was observed with new insertion of fibers in specimens treated with BM-MSCs within 30 days. Conclusion: Both forms of cell transport, BMAC and BM-MSCs, promoted bone formation. However, early bone formation and maturation were achieved when cultured BM-MSCs were used. Likewise, only cultured BM-MSCs were capable of achieving complete periodontal regeneration with inserted fibers in the new cementum-like tissue. (AU)

• Processo FAPESP: 14/03516-0 - Medula óssea e células tronco na regeneração periodontal: análises microtomográfica, histomorfométrica, imunohistoquímica e imunoenzimática em defeitos periodontais de fenestração em ratos
• Beneficiário: Michel Reis Messora
• Modalidade de apoio: Auxílio à Pesquisa - Regular