Title of article :
Comparison of Adhesion and Proliferation of Human Gingival Fibroblasts on Acellular Dermal Matrix with and without Low Level Diode Laser Irradiation, an in vitro Study
Author/Authors :
Taghva ، Orod Dept. of Periodontics - Faculty of Dentistry - Islamic Azad University, Isfahan (Khorasgan) Branch , Amini Sedeh ، Shrin Dept. of Periodontics - Faculty of Dentistry - Islamic Azad University, Isfahan (Khorasgan) Branch , Ejeian ، Fatemeh Dept. of Animal Biotechnology - Cell Science Research Center, Royan Institute for Biotechnology - Academic Center for Education, Culture and Research , Amini ، Shahram Dept. of Periodontics - Faculty of Dentistry - Islamic Azad University, Isfahan (Khorasgan) Branch
From page :
106
To page :
112
Abstract :
Statement of the Problem: In recent years, regeneration of periodontal soft tissues in the reconstruction of periodontal defects and the finding of suitable membranes and graft ma-terials for the placement of autogenous grafts have been of great interest in various studies. In this regard, the proliferation and adhesion of regenerative cells are two linchpins of the complete regenerative process. Purpose: This study aimed to evaluate the effects of low-level laser beams on the attach-ment and the proliferation of human gingival fibroblasts in the presence of acellular dermal matrix (ADM). Materials and Method: All the experiments were conducted compared to tissue culture plate in four groups as follows: (1) Fibroblast+ADM+laser, (2) Fibroblast+ADM+ no laser, (3) Fibroblast + laser radiation, and (4) Fibroblast+ no laser. In this experimental study, the primary attachment was evaluated by passing 8h from seeding of 5×10^5 gingival fibroblasts with or without a single dose (15.6 J/cm^2) of laser radiation. Cell proliferation rate was also examined at 24, 48, and 72 hours after cell culture, following exposure to 5.2 J/cm^2 of laser at each day of examination. Thereafter, fibroblasts were incubated under the normal culture condition (at 37°C, 5% CO2) in high glucose Dulbecco s Modified Eagle s medium (DMEM) medium supplemented with 10% fetal bovine serum, 1% glutamax, and 1% penicillin/streptomycin. Subsequently, the cellular viability was assessed on each time point using MTS calorimetric assay. The obtained data were statistically analyzed by ap-plying ANOVA and Tukey tests. Results: There was a significant difference among the means of these four groups in terms of the proliferation of fibroblasts at 24, 48 and 72 hours (p 0.001). Moreover, there was no significant difference among the means of two groups in terms of fibroblastic attach-ment in 8 hours (p 0.2). The fibroblast group has shown the highest proliferation rate among all groups after laser radiation. Conclusion: It was indicated that the laser radiation increases the fibroblast cell prolifera-tion. Accordingly, although this increase was higher in the fibroblast group alone com-pared to the fibroblasts cultured on acellular dermal matrix, the laser radiation did not significantly increase the attachment of fibroblast cells to acellular dermal matrix.
Keywords :
Acellular Dermal , Fibroblasts , Lasers , Cell Proliferation
Journal title :
Journal of Dentistry :Shiraz University of Medical Sciences
Journal title :
Journal of Dentistry :Shiraz University of Medical Sciences
Record number :
2709029
Link To Document :
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