Chinese Journal of Tissue Engineering Research

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Stably upregulating expression of chondromodulin-Ⅰ in bone marrow mesenchymal stem cells

Zhou Lian-zhong1, Cui Cheng-hua2, Feng Ya3, Xing Shuang-chun3, Zhai Li-jie3   

  1. 1Otolaryngology Head and Neck Surgery Hospital of Tianjin, Tianjin 4th Centre Hospital, Tianjin  300161, China; 2Beijing Cancer Hospital & Beijing Institute for Cancer Research, Peking University, Beijing  100036, China; 3First Affiliated Hospital of Dalian Medical University, Dalian  116011, Liaoning Province, China
  • Revised:2013-04-27 Online:2013-11-05 Published:2013-11-05
  • Contact: Zhai Li-jie, Professor, Master’s supervisor, First Affiliated Hospital of Dalian Medical University, Dalian 116011, Liaoning Province, China lijiezhai@yahoo.com.cn
  • About author:Zhou Lian-zhong★, Master, Physician, Otolaryngology Head and Neck Surgery Hospital of Tianjin, Tianjin 4th Centre Hospital, Tianjin 300161, China zhoulianzhong18@126.com
  • Supported by:

    Funding: the National Natural Science Foundation of China, No. 81271720 2012*; the General Program of Science Research of Liaoning Educational Bureau, No. L2012326 2012*

Abstract:

BACKGROUND: Chondromodulin-Ⅰ is expressed mainly in the cartilage, but it is little expressed in mesenchymal stem cells. Combined with the previous study of our group, we concluded that chondromodulin-Ⅰ maybe play an important role in inducing mesenchymal stem cells into chondrocytes accurately.
OBJECTIVE: To construct an expression plasmid stably carrying chondromodulin-Ⅰ to up-regulate the expression of chondromodulin-Ⅰ in bone marrow mesenchymal stem cells.
METHODS: Specific primers were designed in rat cartilage for chondromodulin-Ⅰ gene, then the pcDNA3.1 (+) plasmid expression vector was digested by enzyme and directional connected gene to construct pcDNA3.1(+)/ChM-Ⅰ expression vector. Bone marrow mesenchymal stem cells were obtained from rats using the method of density gradient centrifugation combined with adherent culture. Recombinant plasmid pcDNA3.1(+)/ChM-Ⅰ was transfected into rat bone marrow mesenchymal stem cells with liposome method, and G418 selection was used for stable screen of transfected cells. Reverse transcription-PCR and western blot were used to detect chondromodulin-Ⅰ expression in cell lines.
RESULTS AND CONCLUSION: The positive clones were digested by enzyme and were identified and sequenced. The results showed that the reality length and sequence of chondromodulin-Ⅰ gene were consistent with the theoretical values, and reading frame was correct. Reverse transcription-PCR and western blot results showed that the expressions of chondromodulin-ⅠmRNA and protein were markedly up-regulated in bone marrow mesenchymal stem cells. Recombinant plasmid pcDNA3.1(+)/ChM-I was successfully constructed, and transfected into rat bone marrow mesenchymal stem cells. After G418 selection, expression of chondromodulin-Ⅰ was up-regulated stably in rat bone marrow mesenchymal stem cells.

Key words: stem cells, mesenchymal stem cells, chondrocytes, glycoproteins

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