Differentiation of human endometrial stem cells into urothelial cells on a three-dimensional nanofibrous silk-collagen scaffold: an autologous cell resource for reconstruction of the urinary bladder wall

Reconstruction of the bladder wall via in vitro differentiated stem cells on an appropriate scaffold could be used in such conditions as cancer and neurogenic urinary bladder. This study aimed to examine the potential of human endometrial stem cells (EnSCs) to form urinary bladder epithelial cells (...

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Veröffentlicht in:Journal of tissue engineering and regenerative medicine 2015-11, Vol.9 (11), p.1268-1276
Hauptverfasser: Shoae-Hassani, Alireza, Mortazavi-Tabatabaei, Seyed Abdolreza, Sharif, Shiva, Seifalian, Alexander Marcus, Azimi, Alireza, Samadikuchaksaraei, Ali, Verdi, Javad
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container_end_page 1276
container_issue 11
container_start_page 1268
container_title Journal of tissue engineering and regenerative medicine
container_volume 9
creator Shoae-Hassani, Alireza
Mortazavi-Tabatabaei, Seyed Abdolreza
Sharif, Shiva
Seifalian, Alexander Marcus
Azimi, Alireza
Samadikuchaksaraei, Ali
Verdi, Javad
description Reconstruction of the bladder wall via in vitro differentiated stem cells on an appropriate scaffold could be used in such conditions as cancer and neurogenic urinary bladder. This study aimed to examine the potential of human endometrial stem cells (EnSCs) to form urinary bladder epithelial cells (urothelium) on nanofibrous silk–collagen scaffolds, for construction of the urinary bladder wall. After passage 4, EnSCs were induced by keratinocyte growth factor (KGF) and epidermal growth factor (EGF) and seeded on electrospun collagen‐V, silk and silk–collagen nanofibres. Later we tested urothelium‐specific genes and proteins (uroplakin‐Ia, uroplakin‐Ib, uroplakin‐II, uroplakin‐III and cytokeratin 20) by immunocytochemistry, RT–PCR and western blot analyses. Scanning electron microscopy (SEM) and histology were used to detect cell–matrix interactions. DMEM/F12 supplemented by KGF and EGF induced EnSCs to express urothelial cell‐specific genes and proteins. Either collagen, silk or silk–collagen scaffolds promoted cell proliferation. The nanofibrous silk–collagen scaffolds provided a three‐dimensional (3D) structure to maximize cell‐matrix penetration and increase differentiation of the EnSCs. Human EnSCs seeded on 3D nanofibrous silk–collagen scaffolds and differentiated to urothelial cells provide a suitable source for potential use in bladder wall reconstruction in women. Copyright © 2013 John Wiley & Sons, Ltd.
doi_str_mv 10.1002/term.1632
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subjects Adult
Biocompatible Materials - pharmacology
biomarker
Cell Culture Techniques
Cell Differentiation
Cells, Cultured
Collagen - chemistry
cytokeratin
differentiation
Endometrium - cytology
Enzyme-Linked Immunosorbent Assay
Epidermal Growth Factor - metabolism
Female
Fibroblast Growth Factor 7 - metabolism
Humans
Immunohistochemistry
Keratinocytes - cytology
Microscopy, Electron, Scanning
Nanofibers - chemistry
Phenotype
Regenerative medicine
Silk - chemistry
stem cell
Stem Cells - cytology
Tissue engineering
Tissue Engineering - methods
Tissue Scaffolds - chemistry
Urinary Bladder - pathology
uroplakin
urothelium
Urothelium - cytology
Urothelium - pathology
title Differentiation of human endometrial stem cells into urothelial cells on a three-dimensional nanofibrous silk-collagen scaffold: an autologous cell resource for reconstruction of the urinary bladder wall
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