Laser therapy increases the proliferation of preosteoblastic MC3T3-E1 cells cultured on poly(lactic acid) films

被引:8
作者
Sabino, Vladimir Galdino [1 ]
Ginani, Fernanda [1 ]
da Silva, Talita Nascimento [2 ]
Cabral, Amanda Alencar [1 ]
Mota-Filho, Haroldo Gurgel [1 ]
Liberato Cavalcanti Freire, Marjorie Caroline [1 ]
Furtado, Priscila de Souza [3 ]
Meireles Carreiros Assumpcao, Paloma Wetler [3 ]
Cabral, Lucio Mendes [3 ]
Moura, Carlos Eduardo [4 ]
Oliveira Rocha, Hugo Alexandre [5 ]
de Souza Picciani, Paulo Henrique [2 ]
Galvao Barboza, Carlos Augusto [1 ]
机构
[1] Univ Fed Rio Grande do Norte, Dept Morphol, Natal, RN, Brazil
[2] Univ Fed Rio de Janeiro, Inst Macromol, Rio De Janeiro, Brazil
[3] Univ Fed Rio de Janeiro, Fac Pharm, Rio De Janeiro, Brazil
[4] Fed Rural Univ Semiarid Reg, Dept Anim Sci, Mossoro, Brazil
[5] Univ Fed Rio Grande do Norte, Dept Biochem, Natal, RN, Brazil
关键词
biomaterials; cell proliferation; cell viability; laser biostimulation; osteoblasts; polymers; MESENCHYMAL STEM-CELLS; PRE-OSTEOBLAST GROWTH; IN-VITRO; IRRADIATION; SCAFFOLDS; BIOCOMPATIBILITY; TERPOLYESTER; PHOTOTHERAPY; PROMOTES;
D O I
10.1002/term.3134
中图分类号
Q813 [细胞工程];
学科分类号
摘要
This study aimed to verify the efficacy of low-level laser irradiation (LLLI) on the proliferation of MC3T3-E1 preosteoblasts cultured on poly(lactic acid) (PLA) films. The produced films were characterized by contact angle tests, scanning electron microscopy (SEM), atomic force microscopy, differential scanning calorimetry, and X-ray diffraction. The MC3T3-E1 cells were cultured as three different groups: Control-cultured on polystyrene plastic surfaces; PLA-cultured on PLA films; and PLA + Laser-cultured on PLA films and submitted to laser irradiation (660 nm; 30 mW; 4 J/cm(2)). Cell proliferation was analyzed by Trypan blue and Alamar blue assays at 24, 48, and 72 h after irradiation. Cell viability was assessed by Live/Dead assay, apoptosis-related events were evaluated by Annexin V/propidium iodide (PI) expression, and cell cycle events were analyzed by flow cytometry. Cell morphology on the surface of films was assessed by SEM. Cell counting and biochemical assay results indicate that the PLA + Laser group exhibited higher proliferation (p< 0.01) when compared with the Control and PLA groups. The Live/Dead and Annexin/PI assays indicate increased cell viability in the PLA + Laser group that also presented a higher percentage of cells in the proliferative cell cycle phases (S and G2/M). These findings were also confirmed by the higher cell density observed in the irradiated group through SEM images. The evidence from this study supports the idea that LLLI increases the proliferation of MC3T3-E1 cells on PLA surfaces, suggesting that it can be potentially applied in bone tissue engineering.
引用
收藏
页码:1792 / 1803
页数:12
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