Chinese Journal of Tissue Engineering Research ›› 2016, Vol. 20 ›› Issue (52): 7796-7802.doi: 10.3969/j.issn.2095-4344.2016.52.006

Previous Articles     Next Articles

Magnetic resonance imaging of canine oral epithelial cells labeled with ultrasmall superparamagnetic iron oxide

Zhou Shu-kui1, Yao Ting-ting2, Zhang Kai-le1, Zou Qing-song1, Fu Qiang1
  

  1. 1Department of Urinary Surgery, 2Department of Radiology, Affiliated Sixth People’s Hospital, Shanghai Jiao Tong University, Shanghai 200233, China
  • Received:2016-09-19 Online:2016-12-16 Published:2016-12-16
  • Contact: Fu Qiang, Professor, Doctoral supervisor, Chief physician, Department of Urinary Surgery, Affiliated Sixth People’s Hospital, Shanghai Jiao Tong University, Shanghai 200233, China
  • About author:Zhou Shu-kui, Studying for doctorate, Physician, Department of Urinary Surgery, Affiliated Sixth People’s Hospital, Shanghai Jiao Tong University, Shanghai 200233, China Yao Ting-ting, Master, Technician, Department of Radiology, Affiliated Sixth People’s Hospital, Shanghai Jiao Tong University, Shanghai 200233, China Zhou Shu-kui and Yao Ting-ting contributed equally to this work.
  • Supported by:

    the National Natural Science Foundation of China, No. 81270780; the Subject of Shanghai Sixth People’s Hospital, No. 1711

Abstract:

BACKGROUND: Epithelial cells are commonly used as the seed cell in tissue engineering; however, there is still a lack of an effective in vivo noninvasive trace technology.
OBJECTIVE: To investigate the feasibility of labeling canine oral epithelial cells with ultrasmall superparamagnetie iron oxide (USPIO) and magnetic resonance imaging (MRI) in vitro. 
METHODS: Oral epithelial cells from beagles were primary cultured, and then labeled by 0.75 mg/L poly-L-lysine combined with USPIO (0, 5, 10, 25, 50 and 100 mg/L), respectively. To determine the optimal dosage, the intracellular iron expression was identified by Prussian blue staining, and the cell viability in different groups was detected by cell counting kit-8. Finally, 2×105 labeled cells were suspended with 1 mL PBS buffer, and were screened using 3.0 T MR on T2*WI sequences in vitro. 
RESULTS AND CONCLUSION: USPIO prepared with 0.75 mg/L poly-L-lysine could successfully label dog oral epithelial cells. Prussian blue staining showed intracellular blue spots, and the intracellular blue spots became more with the concentration increasing and saturated at the concentration of 25 mg/L. Cell counting kit-8 indicated that the cell viability did not change when the concentration < 25 mg/L. Among the T2*WI sequences, the MRI signal intensity decreased with the concentration increasing. In conclusion, canine oral epithelial cells can be effectively labeled with USPIO making no impact on cell viability when the concentration < 25 mg/L, and MRI can be used to track these labeled cells in vitro.

Key words: Iron Compounds, Nanostructures, Magnetic Resonance Imaging, Epithelial Cells, Tissue Engineering

CLC Number: