TY - JOUR
T1 - Comparison of transforming growth factor 1 (Tgf-β1) expression in various lysate platelet-rich fibrin (l-prf) concentrations on human dental pulp stem cell differentiation
AU - Haq, Muhammad Zaal
AU - Margono, Anggraini
AU - Nilakesuma Djauharie, R. A.H.
AU - Asrianti, Dini
AU - Topanesa, Indra
AU - Julianto, Indah
N1 - Funding Information:
We thank our colleagues, Yanni Dirgantara S. Si and Emilia Rahmadaniah Utami, S. Si, from ProSTEM Laboratory, and other collaborators for their excellent experimental assistance and discussions.
Publisher Copyright:
© 2021, Association of Support to Oral Health Research (APESB). All rights reserved.
PY - 2021
Y1 - 2021
N2 - Objective: To compare Transforming growth factor-β1 (TGF-β1) expression in various L-PRF concentrations on the hDPSC differentiation process. Material and Methods: hDPSC cell cultures were subjected to serum starvation by reducing FBS levels in the hDPSC culture media. Lysate PRF was obtained from the PRF gel, which was then incubated at 4°C for 24 h. The supernatant was dried, transferred to a 2-ml Eppendorf tube, and stored at −20°C. The evaluation of TGF-β1 expression in 1%, 5%, 10%, and 25% L-PRF samples and 10% FBS (control) during the process of hDPSC differentiation was quantified using an ELISA reader on day 7. The expression of TGF-β1 was subjected to a one-way ANOVA test, followed by Bonferroni’s post hoc test with significant values (p<0.05). Results: Significant differences were noted in TGF-β1 expression between 1%, 5%, 10%, and 25% L-PRF and the control group (10% FBS). The highest TGF-β1 expression occurred with 25% L-PRF (0.645 ± 0.048), followed by 10% L-PRF (0.461 ± 0.035), 10% FBS (0.374 ± 0.013), 5% L-PRF (0.275 ± 0.045), and the lowest expression was with 1% L-PRF (0.160 ± 0.045). Conclusion: The best result of TGF-B1 expression in hDPSC differentiation was in the 25% L-PRF group.
AB - Objective: To compare Transforming growth factor-β1 (TGF-β1) expression in various L-PRF concentrations on the hDPSC differentiation process. Material and Methods: hDPSC cell cultures were subjected to serum starvation by reducing FBS levels in the hDPSC culture media. Lysate PRF was obtained from the PRF gel, which was then incubated at 4°C for 24 h. The supernatant was dried, transferred to a 2-ml Eppendorf tube, and stored at −20°C. The evaluation of TGF-β1 expression in 1%, 5%, 10%, and 25% L-PRF samples and 10% FBS (control) during the process of hDPSC differentiation was quantified using an ELISA reader on day 7. The expression of TGF-β1 was subjected to a one-way ANOVA test, followed by Bonferroni’s post hoc test with significant values (p<0.05). Results: Significant differences were noted in TGF-β1 expression between 1%, 5%, 10%, and 25% L-PRF and the control group (10% FBS). The highest TGF-β1 expression occurred with 25% L-PRF (0.645 ± 0.048), followed by 10% L-PRF (0.461 ± 0.035), 10% FBS (0.374 ± 0.013), 5% L-PRF (0.275 ± 0.045), and the lowest expression was with 1% L-PRF (0.160 ± 0.045). Conclusion: The best result of TGF-B1 expression in hDPSC differentiation was in the 25% L-PRF group.
KW - Cell Differentiation
KW - Culture Media
KW - Dental Pulp
KW - Platelet-Rich Fibrin
UR - http://www.scopus.com/inward/record.url?scp=85112775226&partnerID=8YFLogxK
U2 - 10.1590/pboci.2021.043
DO - 10.1590/pboci.2021.043
M3 - Article
AN - SCOPUS:85112775226
SN - 1519-0501
VL - 21
JO - Pesquisa Brasileira em Odontopediatria e Clinica Integrada
JF - Pesquisa Brasileira em Odontopediatria e Clinica Integrada
M1 - e5890
ER -