کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5434229 | 1509140 | 2017 | 15 صفحه PDF | دانلود رایگان |
- Aligned nanofibrous scaffolds have been successfully developed to mimick the native architecture of the esophagus.
- Labelled epithelial cells and smooth muscle cells were cultured on these matrices and tracked using confocal microscopy.
- Results demonstrate that both epithelial cells and smooth muscle cells attached well and exhibited extended morphology.
- ECs and SMCs tend to separate into two distinct layers on a single nanofiber system mimicking the in vivo anatomy.
Esophagus is a complex, hollow organ consisting of epithelial cells in the inner mucosal layer and smooth muscle cells in the outer muscle layer. In the present study, we have evaluated the in vitro co-culture of epithelial cells and smooth muscle cells on the aligned nanofibrous scaffold made of PHBV, PHBV-gelatin, PCL and PCL-gelatin developed through electrospinning using rotating drum collector. Epithelial cells were labeled with cell tracker green while the smooth muscle cells were labeled with cell tracker red. Labeled cells were seeded on the aligned nanofibers matrices and tracked using laser scanning confocal microscopy. The results demonstrate that both epithelial and smooth muscle cells attach, extend, and proliferate over these nanofibrous matrices. Confocal z-sectioning shows that epithelial and smooth muscle cells tend to separate into two distinct layers on a single nanofiber system mimicking the in vivo anatomy. Cell viability assay showed that both types of cells are viable and also interact with each other. The functional gene expression of respective cell types demonstrates that both epithelial and smooth muscle cells are phenotypically as well as functionally active when they were co-cultured. Thus the study highlighted that aligned nanofibrous scaffolds could be potential alternative graft for esophageal tissue regeneration.
Journal: Materials Science and Engineering: C - Volume 81, 1 December 2017, Pages 191-205