Chinese Journal of Tissue Engineering Research ›› 2015, Vol. 19 ›› Issue (24): 3808-3812.doi: 10.3969/j.issn.2095-4344.2015.24.008

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Pirfenidone effects on human hypertrophic scar fibroblasts cultured in vitro 

Lan Wei1, Li Xiao-jian2, Ji Xue-liang1, Yi Xian-feng1, Liu Yan-zhi1, Tu Rong-mei1   

  1. 1Department of Burn Rehabilitation, Guangdong Provincial Work Injury Rehabilitation Hospital, Guangzhou 510440, Guangdong Province, China; 
    2First Clinical Medical College of Jinan University, Department of Burns and Plastic Surgery, Guangzhou Red Cross Hospital, Guangzhou 510220, Guangdong Province, China
  • Online:2015-06-11 Published:2015-06-11
  • Contact: Li Xiao-jian, Master, Chief physician, First Clinical Medical College of Jinan University, Department of Burns and Plastic Surgery, Guangzhou Red Cross Hospital, Guangzhou 510220, Guangdong Province, China
  • About author:Lan Wei, Master, Associate chief physician, Department of Burn Rehabilitation, Guangdong Provincial Work Injury Rehabilitation Hospital, Guangzhou 510440, Guangdong Province, China
  • Supported by:

    the Guangdong Medical Science and Technology Research Foundation, No. B2012300

Abstract:

BACKGROUND: Studies have shown that cytokine inhibitor pirfenidone can inhibit biological activity of fibroblasts by regulating a variety of cytokines. It has made good progress in the research and application of anti-fibrosis of internal organs, but the effect and mechanism for hypertrophic scars and skin fibroblasts are unclear.
OBJECTIVE: To investigate the effect of pirfenidone on human hypertrophic scar fibroblasts.
METHODS: Human hypertrophic scar fibroblasts were cultured using tissue culture method. Passages 3-6 cells grew well in the logarithmic growth phase were collected. Cells were divided into the control group (0 g/L pirfenidone), 0.15, 0.3 and 1 g/L pirfenidone groups according to different mass concentrations. Cells were intervened for 12, 36 and 48 hours.
RESULTS AND CONCLUSION: MTT, reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay results demonstrated that compared with the control group, cell proliferation, transforming growth factor β1 mRNA expression, types I and III collagen secretion were decreased in the 0.15, 0.3 and 1 g/L pirfenidone groups (P < 0.05), and the decrease was most significant in the 1 g/L pirfenidone group (P < 0.05). At 24, 48 and 72 hours after intervention, significant differences in inhibitory rate of cell proliferation and the  
secretion of types I and III collagen were detected among 0.15, 0.3 and 1 g/L pirfenidone groups (P < 0.05). Results confirmed that pirfenidone apparently inhibited the secretion of collagen of hypertrophic scar fibroblasts cultured in vitro, transforming growth factor β1 expression and cell proliferation and viability. 


中国组织工程研究杂志出版内容重点:干细胞;骨髓干细胞;造血干细胞;脂肪干细胞;肿瘤干细胞;胚胎干细胞;脐带脐血干细胞;干细胞诱导;干细胞分化;组织工程

Key words: Cytokines, Transforming Growth Factor beta1, Cell Proliferation, Cicatrix, Fibroblasts

CLC Number: