Chinese Journal of Tissue Engineering Research ›› 2010, Vol. 14 ›› Issue (32): 6068-6072.doi: 10.3969/j.issn.1673-8225.2010.32.040

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Feridex labeling of bone marrow stromal cells of crab-eating macaque

Chen Xia1, Yang Zhi-jun2, Luo Yong-chun2, Cai Ying-qian3, Du Mou-xuan3, Zou Yu-xi3   

  1. 1 Pediatric Department, the 324 Hospital of Chinese PLA, Chongqing   400020, China; 2 Department of Neurosurgery, General Hospital of Beijing Military Area Command of Chinese PLA, Beijing   100700, China; 3 Department of Neurosurgery, Zhujiang Hospital, Southern Medical University, Guangzhou   510282, Guangdong Province, China
  • Online:2010-08-06 Published:2010-08-06
  • Contact: Yang Zhi-jun, Associate chief physician, Department of Neurosurgery, General Hospital of Beijing Military Area Command of Chinese PLA, Beijing 100700, China zhijunyangfmmu@yahoo.com.cn
  • About author:Chen Xia★, Master, Attending physician, Pediatric Department, the 324 Hospital of Chinese PLA, Chongqing 400020, China 06chenxia@163.com
  • Supported by:

     Medical Scientific Research Plan of Chengdu Military Area Command of Chinese PLA, No. MB07005*

Abstract:

BACKGROUND: Studies regarding Feridex in vitro cell labeling are mainly in rodents, while little information is known on primate crab-eating macaque.
OBJECTIVE: To explore the feasibility of protocols using Feridex and transfection agents for in vitro magnetic labeling of bone marrow stromal cells (BMSCs) in crab-eating macaque.
METHODS: Under the sterile condition, the crab-eating macaque BMSCs were obtained by means of density gradient centrifugation following a bone puncture. Feridex-poly-l-lysine complexes were used to magnetically label BMSCs. The efficiency and cellular viability of Feridex-poly-l-lysine labeled BMSCs were evaluated by Prussian blue staining, electron microscopy, and trypan blue dye exclusion test. The proliferation and differentiation ability of Feridex-poly-l-lysine labeling BMSCs were also investigated by inverted phase contrast microscope and immunocytochemistry.
RESULTS AND CONCLUSION: BMSCs could be effectively labeled by Feridex and labeling efficiency was around 99%. Tiny blue stained fine particles and numerous vesicles coated with the electron-dense magnetic iron particles could be found in the cytoplasm of Feridex-poly-l-lysine labeled BMSCs under optical microscopy and transmission electron microscopy respectively. Cell viability, proliferation and differentiation ability of labeled BMSCs were not affected by Feridex-poly-l-lysine labeling. Results indicated that Feridex might be used to label BMSCs of crab-eating macaque.

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