TY - JOUR
T1 - Human umbilical cord mesenchymal stem cells accelerate and increase implant osseointegration in diabetic rats
AU - Kuntjoro, Mefina
AU - Hendrijantini, Nike
AU - Prasetyo, Eric Priyo
AU - Legowo, Djoko
AU - Sitalaksmi, Ratri Maya
AU - Agustono, Bambang
AU - Ari, Muhammad Dimas Aditya
AU - Hong, Guang
N1 - Publisher Copyright:
© 2023, Faculdade de Odontologia de Bauru da Universidade de Sao Paulo. All rights reserved.
PY - 2023
Y1 - 2023
N2 - Objective: This study was conducted to assess the effect of hUCMSCs injection on the osseointegration of dental implant in diabetic rats via Runt-related Transcription Factor 2 (Runx2), Osterix (Osx), osteoblasts, and Bone Implant Contact (BIC). Methodology: The research design was a true experimental design using Rattus norvegicus Wistar strain. Rattus norvegicus were injected with streptozotocin to induce experimental diabetes mellitus. The right femur was drilled and loaded with titanium implant. Approximately 1 mm from proximal and distal implant site were injected with hUCMSCs. The control group was given only gelatin solvent injection. After 2 and 4 weeks of observation, the rats were sacrificed for further examination around implant site using immunohistochemistry staining (RUNX2 and Osterix expression), hematoxylin eosin staining, and bone implant contact area. Data analysis was done using ANOVA test. Results: Data indicated a significant difference in Runx2 expression (p<0.001), osteoblasts (p<0.009), BIC value (p<0.000), and Osterix expression (p<0.002). In vivo injection of hUCMSCs successfully increased Runx2, osteoblasts, and BIC value significantly, while decreased Osterix expression, indicating an acceleration of the bone maturation process. Conclusion: The results proved hUCMSCs to accelerate and enhance implant osseointegration in diabetic rat models.
AB - Objective: This study was conducted to assess the effect of hUCMSCs injection on the osseointegration of dental implant in diabetic rats via Runt-related Transcription Factor 2 (Runx2), Osterix (Osx), osteoblasts, and Bone Implant Contact (BIC). Methodology: The research design was a true experimental design using Rattus norvegicus Wistar strain. Rattus norvegicus were injected with streptozotocin to induce experimental diabetes mellitus. The right femur was drilled and loaded with titanium implant. Approximately 1 mm from proximal and distal implant site were injected with hUCMSCs. The control group was given only gelatin solvent injection. After 2 and 4 weeks of observation, the rats were sacrificed for further examination around implant site using immunohistochemistry staining (RUNX2 and Osterix expression), hematoxylin eosin staining, and bone implant contact area. Data analysis was done using ANOVA test. Results: Data indicated a significant difference in Runx2 expression (p<0.001), osteoblasts (p<0.009), BIC value (p<0.000), and Osterix expression (p<0.002). In vivo injection of hUCMSCs successfully increased Runx2, osteoblasts, and BIC value significantly, while decreased Osterix expression, indicating an acceleration of the bone maturation process. Conclusion: The results proved hUCMSCs to accelerate and enhance implant osseointegration in diabetic rat models.
KW - Dental implants
KW - Diabetes mellitus
KW - Mesenchymal stem cells
KW - Osseointegration
KW - Umbilical cord
UR - http://www.scopus.com/inward/record.url?scp=85151573717&partnerID=8YFLogxK
U2 - 10.1590/1678-7757-2022-0375
DO - 10.1590/1678-7757-2022-0375
M3 - Article
C2 - 36995883
AN - SCOPUS:85151573717
SN - 1678-7757
VL - 31
JO - Journal of Applied Oral Science
JF - Journal of Applied Oral Science
M1 - e20220375
ER -