Chinese Journal of Tissue Engineering Research ›› 2011, Vol. 15 ›› Issue (15): 2847-2850.doi: 10.3969/j.issn.1673-8225.2011.15.045

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Effects of synthetic peptides FG loop on PC12 cells proliferation and apoptosis

Fu Hong-long, Ma Xue-xiao, Yu Teng-bo, Chen Bo-hua, Li Ning   

  1. Affiliated Hospital of Qingdao University Medical College, Qingdao  266003, Shandong Province, China
  • Received:2010-12-01 Revised:2011-02-25 Online:2011-04-09 Published:2013-11-06
  • Contact: Chen Bo-hua, Master, Chief physician, Affiliated Hospital of Qingdao University Medical College, Qingdao 266003, Shandong Province, China bohuachen@hotmail.com
  • About author:Fu Hong-long★, Studying for master’s degree, Affiliated Hospital of Qingdao University Medical College, Qingdao 266003, Shandong Province, China fuhonglong@126. com
  • Supported by:

    Research Award Fund for Young Scientists in Shandong Province, No. 2007BS03047*; Science and Technology Development Plan of Qingdao City, No. 06-2-2-6 nsh-2*

Abstract:

BACKGROUND: FG loop (FGL) is a core active peptide fragment of neural cell adhesion molecule (NCAM), which can directly act on fibroblast growth factor receptor 1 (FGFR1) to activate NCAM signal pathway.
OBJECTIVE: To observe the effects of synthetic peptides FGL on PC12 cells proliferation and apoptosis.
METHODS: ①PC12 cells proliferation and apoptosis: The cultured PC12 cells were divided into control group and experiment group. The experimental group was added with 1% FGL peptide solution. The control group was pre-coated with poly-lysine plates. The cells were cultured 1, 3, 5, 7, 9 d respectively to detect cell proliferation by using Cell Counting Kit-8. ②PC12 apoptosis and nuclear factor kappa B mRNA detection: The PC12 cells were divided into normal group, experimental group and injury group. H2O2 was added into the injury group for 16 hours stimulation. In the experimental group, H2O2 and FGL were used for 16 hours stimulation. The cell apoptosis were detected by flow cytometry; mRNA expression of nuclear factor kappa B was detected by quantitative fluorescent polymerase chain reaction.
RESULTS AND CONCLUSION: PC12 cells cocultured with FGL peptide grow well, which indicates that FGL peptides can promote PC12 cell proliferation and inhibit PC12 cell apoptosis, as well as decrease mRNA expression of nuclear factor kappa B.

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