Effect of low-power laser irradiation on protein synthesis and ultrastructure of human gingival fibroblasts

被引:128
作者
Marques, MM
Pereira, AN
Fujihara, NA
Nogueira, FN
Eduardo, CP
机构
[1] Univ Sao Paulo, Sch Dent, Dept Operat Dent, BR-05508900 Sao Paulo, SP, Brazil
[2] Univ Sao Paulo, Sch Dent, Dept Stomatol, BR-05508900 Sao Paulo, SP, Brazil
[3] Univ Sao Paulo, Sch Dent, Dept Dent Mat, BR-05508900 Sao Paulo, SP, Brazil
关键词
biostimulation; cell culture; collagen; low-power lasers;
D O I
10.1002/lsm.20008
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background and Objectives: Low-power lasers improve wound healing. Cell proliferation and protein secretion are important steps of this process. The aim of this study was to analyze both protein synthesis and ultrastructural morphology of human gingival fibroblasts irradiated by a low-power laser. Study Design/Materials and Methods: The cell line FMM1 was grown in nutritional deficit. Laser irradiation was carried out with a gallium-aluminum-arsenate (Ga-Al-As) diode laser (904 nm, 120 mW, energy density of 3J/cm(2) 2). The protein synthesis analysis and ultrastructural morphology of control (non-irradiated) and irradiated cultures were obtained. Results: There were changes in the structure of cytoplasm organelles of treated cells. The procollagen was not altered by the laser irradiation; however, there were a significant reduction of the amount of protein in the DMEM conditioned by irradiated cells. Conclusions: Low-power laser irradiation causes ultrastructural changes in cultured fibroblasts. We suggest that these alterations may lead to disturbances in the collagen metabolism. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:260 / 265
页数:6
相关论文
共 22 条
[1]   Comparison of the low level laser therapy effects on cultured human gingival fibroblasts proliferation using different irradiance and same fluence [J].
Almeida-Lopes, L ;
Rigau, J ;
Zângaro, RA ;
Guidugli-Neto, J ;
Jaeger, MMM .
LASERS IN SURGERY AND MEDICINE, 2001, 29 (02) :179-184
[2]   Hypertrophic scars and keloids - Etiology and management [J].
Alster, TS ;
Tanzi, EL .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2003, 4 (04) :235-243
[3]  
BAKEEVA LE, 1993, MOL BIOL+, V27, P369
[4]  
FISHER LW, 1989, CONNECT TISSUE RES, V21, P373
[5]  
FRESHNEY RI, 2000, CULTURE ANIMAL CELLS, P104
[6]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[7]   Low-level laser therapy for wound healing: Feasibility of wound dressing transillumination [J].
Lilge, L ;
Tierney, K ;
Nussbaum, E .
JOURNAL OF CLINICAL LASER MEDICINE & SURGERY, 2000, 18 (05) :235-240
[8]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265
[9]   Effect of transforming growth factor-β1, interleukin-6, and interferon-γ on the expression of type I collagen ,heat shock protein 47, matrix metalloproteinase (MMP)-1 and MMP-2 by fibroblasts from normal gingival and hereditary gingival fibromatosis [J].
Martelli-Junior, H ;
Cotrim, P ;
Graner, E ;
Sauk, JJ ;
Coletta, RD .
JOURNAL OF PERIODONTOLOGY, 2003, 74 (03) :296-306
[10]   Effect of low-power laser irradiation on cell growth and procollagen synthesis of cultured fibroblasts [J].
Pereira, AN ;
Eduardo, CD ;
Matson, E ;
Marques, MM .
LASERS IN SURGERY AND MEDICINE, 2002, 31 (04) :263-267