Laser therapy increases the proliferation of preosteoblastic MC3T3‐E1 cells cultured on poly(lactic acid) films. (7th October 2020)

• Record Type: Journal Article
• Authors: Sabino, Vladimir Galdino; Ginani, Fernanda; da Silva, Talita Nascimento; Cabral, Amanda Alencar; Mota‐Filho, Haroldo Gurgel; Freire, Marjorie Caroline Liberato Cavalcanti; de Souza Furtado, Priscila; Assumpção, Paloma Wetler Meireles Carreiros; Cabral, Lucio Mendes; Moura, Carlos Eduardo; Rocha, Hugo Alexandre Oliveira; de Souza Picciani, Paulo Henrique; Barboza, Carlos Augusto Galvão
• Is Part Of: Journal of tissue engineering and regenerative medicine. Volume 14:Number 12(2020)
• Page Start: 1792
• Page End: 1803
• Publication Date: 2020-10-07
• Subjects: biomaterials -- cell proliferation -- cell viability -- laser biostimulation -- osteoblasts -- polymers; Tissue engineering -- Periodicals; Regeneration (Biology) -- Periodicals; 610.28
• DOI: 10.1002/term.3134
• Languages: English
• ISSNs: 1932-6254

Abstract

Abstract: 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.