Chinese Journal of Tissue Engineering Research ›› 2017, Vol. 21 ›› Issue (34): 5487-8492.doi: 10.3969/j.issn.2095-4344.2017.34.013

Previous Articles     Next Articles

Preparation of porcine small intestinal submucosa sponge and observation of cell adhesion

Sun Hui-zhe1, Tian Wei2, Zeng Liang2, Qiu Jin-yun2, Zhang Qian3
  

  1. 1Center for Medical Education Research, 2Department of Human Anatomy, Shenyang Medical College, Shenyang 110034, Liaoning Province, China; 3Shenyang Medical College, Shenyang 110034, Liaoning Province, China
  • Received:2017-10-30 Online:2017-12-08 Published:2018-01-04
  • About author:Sun Hui-zhe, Master, Associate professor, Center for Medical Education Research, Shenyang Medical College, Shenyang 110034, Liaoning Province, China
  • Supported by:
    the Science Research General Project of Liaoning Provincial Department of Education in 2014, No. L2014416

Abstract:

BACKGROUND: Although the porcine small intestinal submucosa is very similar to the skin in the structure, its pore size and porosity are not beneficial to the growth of seed cells as the skin does.
OBJECTIVE: To observe the morphological and cytocompatibility of porcine small intestinal submucosa after chemical modification using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDC).
METHODS: A porcine small intestinal submucosa sample was immersed in 3% acetic acid solution containing 0.2% pepsin to make 1%, 2%, 3%, 4% small intestine submucosa solutions. After magnetic stirring and freeze-drying, small intestinal submucosa sponge was obtained and modified by cross-linking with 50, 100, 150 mmol/L EDC. Based on the detection of pore size and water absorption, we selected the best concentrations of small intestinal submucosa and EDC, which were further used for cell culture. Passage 2 bone marrow mesenchymal stem cells were cocultured with the small intestinal submucosa sponge, and observed under scanning electron microscope at 1, 2, 3 weeks after co-culture.
RESULTS AND CONCLUSION: When cross-linked with 100 mmol/L EDC, the small intestinal submucosa sponge at a mass concentration of 1% showed a reasonable structure and good elasticity with no appearance of voids, and the pore size ranged 100-150 µm. Moreover, the small intestinal submucosa sponge at a mass concentration of 1% showed a 0.35-fold increase in the compared with that at a mass concentration of 2%, and its structure was more conducive to water flows and changes. The small intestinal submucosa sponges at a mass concentration of 3% and 4% showed no difference in the water absorbing capacity. After cross-linked with 100 mmol/L EDC, the small intestinal submucosa sponge at a mass concentration of 1% showed the best structure, pore size and water absorption, which were used for cell culture. At 3 weeks after cell culture, cell deformation was relatively intact and fast; there were many cells in the pores that were relatively large and approximately spindle-shaped, while there were less cells around the pores that were relatively small and disk-shaped. A paving stone-like alteration was observed in cells that covered the most of the scaffold surface with a large number of particle-like substances, especially in the site of cell concentration. All these findings indicate that EDC-modified small intestinal submucosa sponge has good cytocompatibility. 

Key words: Skin Transplantation, Cell Adhesion, Tissue Engineering

CLC Number: