scholarly journals Isolation and characterization of human dental tissue-derived stem cells in the impacted wisdom teeth: comparison of dental follicle, dental pulp, and root apical papilla-derived cells

Author(s):  
Jung-Ho Song ◽  
Bong-Wook Park ◽  
June-Ho Byun ◽  
Eun-Ju Kang ◽  
Gyu-Jin Rho ◽  
...  
2013 ◽  
Vol 39 (1) ◽  
pp. 31-38 ◽  
Author(s):  
Pakize Neslihan Taşlı ◽  
Sıdıka Tapşın ◽  
Sezin Demirel ◽  
Mehmet Emir Yalvaç ◽  
Serap Akyuz ◽  
...  

2008 ◽  
Vol 37 (9) ◽  
pp. 571-574 ◽  
Author(s):  
Anderson Hsien-Cheng Huang ◽  
Yuk-Kwan Chen ◽  
Lin-Min Lin ◽  
Tien-Yue Shieh ◽  
Anthony Wing-Sang Chan

2006 ◽  
Vol 184 (3-4) ◽  
pp. 105-116 ◽  
Author(s):  
Irina Kerkis ◽  
Alexandre Kerkis ◽  
Dmitri Dozortsev ◽  
Gaëlle Chopin Stukart-Parsons ◽  
Sílvia Maria Gomes Massironi ◽  
...  

2020 ◽  
Vol 23 (1) ◽  
Author(s):  
Jairo Barros Weiss ◽  
Fernanda Da Silva Gonçalves ◽  
Carlos Magno Da Costa Maranduba ◽  
Leandro Marques De Resende ◽  
Antonio Marcio Resende Do Carmo

Objective: The aim of this study was to evaluate the impact on the isolation and characterization of stem cells from pulp tissues obtained through rotary instrumentation techniques compared to the manual technique. Material and Methods: Thirty permanent teeth were included, 15 of which were instrumented with rotational technique (Protaper SX) and other 15 with manual technique. Cells obtained were characterized by flow cytometry and proliferation was evaluated by the MTT assay. The plasticity was evaluated for adipogenic, osteogenic and odontogenic differentiations. Results: Cells isolated from the pulp of permanent teeth, by manual techniques, presented fibroblast morphology and were able to differentiate successfully. All lineages expressed CD29, CD73, CD90, CD105, CD146, CD166 and were negative for CD31, CD34 and CD45. MTT assay showing significantly increased proliferation of hDPSCs in 5 and 7 days of the culture. Conclusion: The present study demonstrated that manual instrumentation technique is one of the best candidates to harvest dental pulp tissue as the dental stem cell source due to ability effective expanded with less tissue invasion. The technique of rotational instrumentation proved to be very harmful to the tissues of the dental pulp, and we can’t obtain cells using this technique.Keywords: Root Canal Therapy; Pulpectomy; Anatomy and Histology; Stem Cell.


PLoS ONE ◽  
2011 ◽  
Vol 6 (11) ◽  
pp. e27526 ◽  
Author(s):  
Kajohnkiart Janebodin ◽  
Orapin V. Horst ◽  
Nicholas Ieronimakis ◽  
Gayathri Balasundaram ◽  
Kanit Reesukumal ◽  
...  

2014 ◽  
Vol 14 (4) ◽  
pp. 327-331 ◽  
Author(s):  
M.R. Nur Akmal ◽  
Z.A. Intan Zari ◽  
M.A.W. Rohaya ◽  
S. Sahidan ◽  
Z.A. Zaidah ◽  
...  

2017 ◽  
Vol 79 (1) ◽  
pp. 47-51 ◽  
Author(s):  
Shingo ISHIKAWA ◽  
Chie HORINOUCHI ◽  
Daiki MURATA ◽  
Shota MATSUZAKI ◽  
Kazuhiro MISUMI ◽  
...  

2018 ◽  
Vol 10 (2) ◽  
pp. 9-18
Author(s):  
Dr. Vinay Rao ◽  
Dr. Roopa R Nadig ◽  
Dr.Ramanand Nadig ◽  
Dr.Karthik .J ◽  
Dr. Veena Pai S

AIMS AND OBJECTIVES: 1. Isolation and growth of dental pulp stem cells (DPSCs) and stem cells from exfoliated human deciduous teeth (SHED). 2. Characterization of dental pulp stem cells (DPSCs) and stem cells from exfoliated human deciduous teeth (SHED). METHODS: The pulp tissue was digested in collagenase and cultured in DMEM Dulbecco’s Modified Eagle’s Media). The stem cells were identified and isolated. Surface characterization of cells was done with the help of flow cytometer using a panel of various surface markers. An immuno cytochemistry analysis was done to see the expression of proteins in the cells. RESULTS: Identification of cells was done with the help of a phase contrast microscope. Flow cytometry analyses for various CD markers showed similar results for both DPSCs and SHED. The cells showed positive expression for pluripotent markers, ectodermal markers and mesodermal markers. CONCLUSION: The study demonstrated that stem cells existed in human deciduous and permanent pulp tissue. The stem cells present in deciduous permanent pulp tissue can be isolated, cultivated and expanded in vitro. Both DPSCs and SHED show almost a similar expression pattern profile for variety of antigens tested. Further studies should include analysis of diverse cell populations to elucidate their potential to differentiate into various cell types followed by in vivo studies in animals and humans.


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