Bone marrow mesenchymal stem cells could acquire the phenotypes of epithelial cells and accelerate vaginal reconstruction combined with small intestinal submucosa

2015 ◽  
Vol 39 (11) ◽  
pp. 1225-1233 ◽  
Author(s):  
Yanan Li ◽  
Fangfang Liu ◽  
Zhiqiang Zhang ◽  
Mingle Zhang ◽  
Shanjin Cao ◽  
...  
2013 ◽  
Vol 9 (3) ◽  
pp. 296-304 ◽  
Author(s):  
Hiroki Nakatsu ◽  
Tomio Ueno ◽  
Atsunori Oga ◽  
Mitsuhiro Nakao ◽  
Taku Nishimura ◽  
...  

2021 ◽  
Vol 11 ◽  
Author(s):  
Lei Wu ◽  
Chao Rong ◽  
Qing Zhou ◽  
Xin Zhao ◽  
Xue-Mei Zhuansun ◽  
...  

Mesenchymal stem cells (MSCs) have regenerative properties in acute kidney injury (AKI). However, the potential function of MSCs in chronic kidney disease remains elusive. Renal fibrosis is the common endpoint of chronic progressive kidney diseases and causes a considerable health burden worldwide. In this study, the protective effects of bone marrow mesenchymal stem cells (BM-MSCs) were assessed in repeated administration of low-dose cisplatin-induced renal fibrosis mouse model in vivo as well as a TGF-β1-induced fibrotic model in vitro. Differentially expressed miRNAs in mouse renal tubular epithelial cells (mRTECs) regulated by BM-MSCs were screened by high-throughput sequencing. We found microRNA (miR)-146a-5p was the most significant up-regulated miRNA in mRTECs. In addition, the gene Tfdp2 was identified as one target gene of miR-146a-5p by bioinformatics analysis. The expression of Tfdp2 in the treatment of BM-MSCs on cisplatin-induced renal injury was evaluated by immunohistochemistry analysis. Our results indicate that BM-MSC attenuates cisplatin-induced renal fibrosis by regulating the miR-146a-5p/Tfdp2 axis in mRTECs.


2005 ◽  
Vol 173 (4S) ◽  
pp. 131-131
Author(s):  
Steve Y. Chung ◽  
Nikolov Krivorov ◽  
Veronica Rausei ◽  
Lisa Thomas ◽  
Maika Frantzen ◽  
...  

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