Chinese Journal of Tissue Engineering Research ›› 2012, Vol. 16 ›› Issue (42): 7925-7928.doi: 10.3969/j.issn.2095-4344.2012.42.026

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Effect of platelet-derived growth factor-BB on proliferation of tendon cells cultured in vitro

Xie Ai-guo1, Liang Hong-wei2   

  1. 1Department of Burns and Plastic Surgery, Second Hospital of Nanjing Medical University, Nanjing 210011, Jiangsu Province, China
    2Department of Burns and Plastic Surgery, Zhengzhou People’s Hospital, Zhengzhou 450003, Henan Province, China
  • Received:2012-01-26 Revised:2012-02-22 Online:2012-10-14 Published:2012-10-14
  • About author:Xie Ai-guo★, Master, Physician, Department of Burns and Plastic Surgery, Second Hospital of Nanjing Medical University, Nanjing 210011, Jiangsu Province, China

Abstract:

BACKGROUND: Cell proliferation and tissue repair is a complicated process, accompanied by participation of multiple growth factors. These factors interact with each other to better promote cell proliferation and tissue repair.
OBJECTIVE: To investigate the effect of platelet-derived growth factor-BB (PDGF-BB) of different concentrations on proliferation of tendon cells cultured in vitro.
METHODS: Rat tendon cells were cultured and identified in vitro. According to concentration of PDGF-BB nutrient solution in culture medium, the cells were divided into control group (0 μg/L) and PDGF-BB groups (1, 5, 10, 20, 50, 100, 150, 200, 250 μg/L). Proliferation of tendon cells was detected by MTT test. The absorbance value of tendon cells in control group and 20 μg/L PDGF-BB group after culture for 12, 24, 36, 48, 60 and 72 hours were determined to evaluate relationship with proliferation dose-effect and time.
RESULTS AND CONCLUSION: The isolated cells were identified to be tendon cells as they were positive for type Ⅰ collagen staining and negative for type Ⅲ collagen staining. Compared with control group, the absorbance values of all groups were all increased, except for 250 μg/L PDGF-BB group (P < 0.05 or P < 0.01). Besides, the absorbance value rose gradually with the increase of the concentration of PDGF-BB, and then diminished gradually with the increase of the concentration of PDGF-BB from 20 μg/L. The number of tendon cells in 20 μg/L PDGF-BB group began to increase when cultured for 12 hours, and reached the highest level at 48 hours, and the absorbance at 24-72 hours was significantly greater than control group (P < 0.01). Results suggest that PDGF-BB can promote the proliferation of tendon cells in a definite range of concentration and time.

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