scholarly journals Evaluation of cell viability of human dental pulp stem cells in two dimensional and three dimensional fibrin glue scaffold

2020 ◽  
Vol 23 (5) ◽  
pp. 479
Author(s):  
NeedaA Ansari ◽  
Abhishek Parmar ◽  
Girish Parmar ◽  
Amee Krishnakumar
Biomaterials ◽  
2006 ◽  
Vol 27 (33) ◽  
pp. 5658-5668 ◽  
Author(s):  
Weibo Zhang ◽  
X. Frank Walboomers ◽  
Toin H. van Kuppevelt ◽  
Willeke F. Daamen ◽  
Zhuan Bian ◽  
...  

2017 ◽  
Vol 28 (4) ◽  
pp. 939-943 ◽  
Author(s):  
María Pilar Pecci-Lloret ◽  
Mar Vera-Sánchez ◽  
Salvador Aznar-Cervantes ◽  
David García-Bernal ◽  
Ricardo Oñate Sánchez ◽  
...  

Cytotherapy ◽  
2013 ◽  
Vol 15 (4) ◽  
pp. 507-518 ◽  
Author(s):  
Miguel Angel Martin-Piedra ◽  
Ingrid Garzon ◽  
Ana Celeste Oliveira ◽  
Camilo Andres Alfonso-Rodriguez ◽  
Maria Carmen Sanchez-Quevedo ◽  
...  

Materials ◽  
2021 ◽  
Vol 14 (10) ◽  
pp. 2684
Author(s):  
Camila Corral Nunez ◽  
Diego Altamirano Gaete ◽  
Miguel Maureira ◽  
Javier Martin ◽  
Cristian Covarrubias

This study aimed to investigate the cytotoxicity and bioactivity of a novel nanocomposite containing nanoparticles of bioactive glass (nBGs) on human dental pulp stem cells (hDPSCs). nBGs were synthesized by the sol–gel method. Biodentine (BD) nanocomposites (nBG/BD) were prepared with 2 and 5% wt of nBG content; unmodified BD and glass ionomer cement were used as references. Cell viability and attachment were evaluated after 3, 7 and 14 days. Odontogenic differentiation was assessed with alkaline phosphatase (ALP) activity after 7 and 14 days of exposure. Cells successfully adhered and proliferated on nBG/BD nanocomposites, cell viability of nanocomposites was comparable with unmodified BD and higher than GIC. nBG/BD nanocomposites were, particularly, more active to promote odontogenic differentiation, expressed as higher ALP activity of hDPSCs after 7 days of exposure, than neat BD or GIC. This novel nanocomposite biomaterial, nBG/BD, allowed hDPSC attachment and proliferation and increased the expression of ALP, upregulated in mineral-producing cells. These findings open opportunities to use nBG/BD in vital pulp therapies.


2012 ◽  
Vol 3 (1) ◽  
pp. 204173141246799 ◽  
Author(s):  
Rashi Khanna-Jain ◽  
Bettina Mannerström ◽  
Annukka Vuorinen ◽  
George KB Sándor ◽  
Riitta Suuronen ◽  
...  

2019 ◽  
Vol 10 ◽  
pp. 204173141984584 ◽  
Author(s):  
Jonghyeuk Han ◽  
Da Sol Kim ◽  
Ho Jang ◽  
Hyung-Ryong Kim ◽  
Hyun-Wook Kang

Numerous approaches have been introduced to regenerate artificial dental tissues. However, conventional approaches are limited when producing a construct with three-dimensional patient-specific shapes and compositions of heterogeneous dental tissue. In this research, bioprinting technology was applied to produce a three-dimensional dentin–pulp complex with patient-specific shapes by inducing localized differentiation of human dental pulp stem cells within a single structure. A fibrin-based bio-ink was designed for bioprinting with the human dental pulp stem cells. The effects of fibrinogen concentration within the bio-ink were investigated in terms of printability, human dental pulp stem cell compatibility, and differentiation. The results show that micro-patterns with human dental pulp stem cells could be achieved with more than 88% viability. Its odontogenic differentiation was also regulated according to the fibrinogen concentration. Based on these results, a dentin–pulp complex having patient-specific shape was produced by co-printing the human dental pulp stem cell–laden bio-inks with polycaprolactone, which is a bio-thermoplastic used for producing the overall shape. After culturing with differentiation medium for 15 days, localized differentiation of human dental pulp stem cells in the outer region of the three-dimensional cellular construct was successfully achieved with localized mineralization. This result demonstrates the possibility to produce patient-specific composite tissues for tooth tissue engineering using three-dimensional bioprinting technology.


Materials ◽  
2019 ◽  
Vol 12 (8) ◽  
pp. 1259 ◽  
Author(s):  
Minsun Chung ◽  
Sukjoon Lee ◽  
Dongzi Chen ◽  
Ukseong Kim ◽  
Yaelim Kim ◽  
...  

This study aimed to analyze the effects of different calcium silicate cements (CSCs) on the inflammatory response and odontogenic differentiation of lipopolysaccharide-stimulated human dental pulp stem cells. Human dental pulp stem cells (hDPSCs) were stimulated with lipopolysaccharide (LPS) to induce inflammation. These LPS-induced dental pulp stem cells (LDPSCs) were cultured with ProRoot MTA, Biodentine, Retro MTA, and Dycal. Cell viability was evaluated using the Cell Counting Kit-8 assay. Interleukin (IL)-6, IL-8, and transforming growth factor (TGF)-β1 cytokine levels were assessed using the enzyme-linked immunosorbent assay. The expressions of alkaline phosphatase (ALP), osteocalcin, and runt-related transcription factor 2 (RUNX2) were analyzed through real-time polymerase chain reaction. ProRoot MTA, Biodentine, and Retro MTA did not significantly decrease the cell viability of LDPSCs for up to 48 h (p < 0.05). Retro MTA significantly decreased the expression of IL-6 and IL-8 by LDPSCs. ProRoot MTA and Biodentine significantly reduced TGF-β expression by LDPSCs (p < 0.05). Regarding odontogenic differentiation, all CSCs had no effect on ALP expression but increased the production of RUNX2 at 12 h.


Sign in / Sign up

Export Citation Format

Share Document