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Biocompatibility of polypropylene mesh scaffold with adipose-derived stem cells.

Authors :
HUI CHENG
YANLING ZHANG
BEI ZHANG
JIE CHENG
WEIQI WANG
XIN TANG
PENG TENG
YANYU LI
Source :
Experimental & Therapeutic Medicine. Jun2017, Vol. 13 Issue 6, p2922-2926. 5p.
Publication Year :
2017

Abstract

In this study, we investigated the rejection of the synthetic patch and human tissues in the host. We observed the growth of adipose-derived stem cells (ADSCs) cultured with polypropylene mesh in vitro. The results of flow cytometry showed that the expression of CD44, CD73, CD90, CD45, CD14 and CD34 was 98.54, 95.32, 98.49, 1.21, 3.01 and 2.14%, respectively. ADSCs were isolated from rabbit subcutaneous adipose tissue after collagenase digestion, filtration and centrifugation. The ADSCs of passage 3 were seeded onto the polypropylene mesh scaffolds. New Zealand White female breeder rabbits were implanted with polypropylene mesh, ADSC-fixed polypropylene mesh in the abdomen. After 4 weeks, adhesion was performed and the erosion of the mesh was evaluated. It was found that polypropylene mesh, ADSC-fixed polypropylene mesh all had different degrees of corrosion, and adhesion, but polypropylene mesh was more corroded. ADSC-fixed polypropylene mesh induced a milder chronic inflammation response compared with polypropylene, had significantly lower scores for inflammation (t=11.083), and had significantly higher scores for neovascularization (t=14.362) and fibroblastic proliferation (t=15.979). The relative amount of VEGF mRNA was significantly lower for ADSCfixed polypropylene compared with the other polypropylene meshes (t=94.6). In conclusion, polypropylene mesh scaffold with ADSCs exhibit excellent cellular compatibility and are promising in clinical practice. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17920981
Volume :
13
Issue :
6
Database :
Academic Search Index
Journal :
Experimental & Therapeutic Medicine
Publication Type :
Academic Journal
Accession number :
123110668
Full Text :
https://doi.org/10.3892/etm.2017.4338