Chinese Journal of Tissue Engineering Research ›› 2016, Vol. 20 ›› Issue (33): 4926-4932.doi: 10.3969/j.issn.2095-4344.2016.33.009

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hIL-24 gene influences the biological characteristics of the keloid by regulating transforming growth factor-beta/Smad pathway

Wu Zhi-yuan1, Shi Yu-cang2, Jiang Jun-jian3, Wu Zhi-xian2, Zhang Hui-jun2, Liu Yan-fang2, Liu Hong-wei1   

  1. 1the First Clinical College of Jinan University, Guangzhou 510632, Guangdong Province, China; 2Department of Plastic Surgery, the Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, Guangdong Province, China; 3Department of Hand Surgery, Huashan Hospital Affiliated to Fudan University, Shanghai 200040, China
  • Received:2016-05-24 Online:2016-08-12 Published:2016-08-12
  • Contact: Liu Hong-wei, M.D., Professor, the First Clinical College of Jinan University, Guangzhou 510632, Guangdong Province, China
  • About author:Wu Zhi-yuan, Master, Professor, the First Clinical College of Jinan University, Guangzhou 510632, Guangdong Province, China
  • Supported by:

    the Science and Technology Research Fund of Zhanjiang, No. 2014B01024

Abstract:

BACKGROUND: hIL-24, a tumor suppressor gene, can stimulate immune responses, inhibit the growth of tumor cells, and the formation of tumor vessels, and induce cell apoptosis.
OBJECTIVE: To explore the effects of hIL-24 gene on the proliferation and apoptosis of fibroblasts in the keloid and the underlying mechanisms.
METHODS: All the keloid specimens collected from 13 patients were used for fibroblast culture and indentification. Fibroblast of the keloid was transfected with or without hlL-24 lentivirus. Subsequently, mRNA expressions of transforming growth factor-β, Smad3, proliferating cell nuclear antigen, matrix metalloproteinase-2, -9, and metallopeptidase inhibitor 1 were determined.
RESULTS AND CONCLUSION: Immunofluorescent staining and flow cytometry showed that vimentin antibody was expressed positively in cytoplasma of fibroblast cultures, and the purity was more than 97.8%. Western blot assay showed that hIL-24 expression was significantly increased in the transfected fibroblasts. Quantitative PCR showed that the overexpression rate of hIL-24 in fibroblasts was 81.7% and mRNA expressions of transforming growth factor-β, Smad3, proliferating cell nuclear antigen, matrix metalloproteinase-2, and -9 were significantly decreased, while metallopeptidase inhibitor 1 mRNA expression was significantly increased in hIL-24 transfection group compared with control group (P < 0.05). These findings suggest that hIL-24 gene inhibits the expressions of proliferating cell nuclear antigen, matrix metalloproteinase-2, and -9 in fibroblasts, and the underlying mechanism may involves TGF-β/Smad3 pathway.

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: Keloid, Matrix Metalloproteinases, Signal Transduction

CLC Number: