Chinese Journal of Tissue Engineering Research ›› 2018, Vol. 22 ›› Issue (36): 5840-5845.doi: 10.3969/j.issn.2095-4344.0697

Previous Articles     Next Articles

Aminolevulinic acid photodynamic therapy can significantly inhibit the growth of endothelial cells and induce cell apoptosis

Ge Wenjia, Ma Xiaorong, Ouyang Tianxiang   

  1. (Department of Plastic Surgery, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China)
  • Received:2018-08-07 Online:2018-12-28 Published:2018-12-28
  • Contact: Ouyang Tianxiang, Department of Plastic Surgery, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
  • About author:Ge Wenjia, Department of Plastic Surgery, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China
  • Supported by:

    the Scientific Research Foundation of Health Bureau of Shanghai, No. 201540374

Abstract:

BACKGROUND: There is a lack of safe and effective method for hypertrophic scar. Fibroblast hypertrophy, vascular endothelial cell hyperplasia and neovascularization are key points for hypertrophic scar formation. Continuous laser radiation has been shown to induce fibroblast apoptosis. Aminolevulinic acid photodynamic therapy (ALA-PDT) has been extensively applied in the treatment of tumor and skin diseases, which provide novel therapy for hypertrophic scar.
OBJECTIVE: To explore the effect of ALA-PDT on endothelial cell apoptosis.
METHODS: Human umbilical vein endothelial cells were cultured in vitro, and divided into four groups: control group (no treatment), single-drug group (incubation with 2 mmol/L 5-aminolevulinic acid), single-light group (3 J/cm2 photodynamic irradiation for 8 minutes) and ALA-PDT group (after incubation with 2 mmol/L 5-aminolevulinic acid for 4 hours, irradiated by 3 J/cm2 photodynamic for 8 minutes, and cultured for 24 hours in dark).
RESULTS AND CONCLUSION: Fluorescence microscopy showed that the accumulation of fluorescence in umbilical vein endothelial cells was ALA-dependent and peaked at a concentration of 2 mmol/L. Cytotoxicity test showed no significant difference in cell viability in the simple-drug group. Cell viability in the ALA-PDT group was significantly inhibited at a drug concentration of 2 and 4 mmol/L (P < 0.01). Hoechst 33258 staining and flow cytometry analysis showed that ALA-PDT could induce cell apoptosis when ALA concentration was 2 mmol/L (P < 0.01). These results indicate that ALA-PDT can significantly inhibit the growth of endothelial cells and induce apoptosis of endothelial cells.

中国组织工程研究杂志出版内容重点:组织构建;骨细胞;软骨细胞;细胞培养;成纤维细胞;血管内皮细胞;骨质疏松组织工程

Key words: Cicatrix, Apoptosis, Endothelial Cells

CLC Number: