Comparison of P75NTR‐positive and ‐negative etcomesenchymal stem cell odontogenic differentiation through epithelial–mesenchymal interaction. (31st March 2016)
- Record Type:
- Journal Article
- Title:
- Comparison of P75NTR‐positive and ‐negative etcomesenchymal stem cell odontogenic differentiation through epithelial–mesenchymal interaction. (31st March 2016)
- Main Title:
- Comparison of P75NTR‐positive and ‐negative etcomesenchymal stem cell odontogenic differentiation through epithelial–mesenchymal interaction
- Authors:
- Xing, Yongjun
Nie, Xin
Chen, Guoqing
Wen, Xiujie
Li, Gang
Zhou, Xia
Tian, Weidong
Liu, Luchuan - Abstract:
- Abstract: Objectives: The aim of this study was to investigate differences of odonto‐differentiation between P75 ‐neurotrophin receptor (P75 ‐NTR)‐positive ectomesenchymal stem cells ( P 75 + EMSCs) and P75 ‐NTR‐negative ectomesenchymal stem cells ( P 75 − EMSCs), and their underlying mechanisms. Materials and methods: Primary cranial neural crest‐derived cells (CNC) were isolated from the first branchial arches, and P 75 + EMSCs and P 75 − EMSCs were sorted by fluorescence‐activated cell sorting. Differentiation of P 75 + EMSCs or P 75 − EMSCs into odontoblast‐like cells was induced by dental epithelial cells in vitro or in vivo . Differential gene expression profiles between P 75 + EMSCs and P 75 − EMSCs were analysed by microarray assay. Smad4‐specific small interfering RNA and activator kartogenin were used to treat the cells, to evaluate effects of Smad4 in odonto‐differentiation of P 75 + EMSCs or P 75 − EMSCs. Results: Under induction of dental epithelium conditioned medium, P 75 + EMSCs had more mineralized node formation and higher expression of Dmp1 and Dspp compared to P 75 − EMSCs. In our in vivo study, graft of P 75 + EMSCs recombination with dental epithelium showed higher expression of DMP1 and DSP. Knock‐down of Smad4 in P 75 + EMSCs significantly downregulated expression of DMP1 and DSP, while activation of Smad4 in P 75 − EMSCs by the activator kartogenin, significantly increased DSP and DMP1 expression. Conclusions: P 75 + EMSCs showed moreAbstract: Objectives: The aim of this study was to investigate differences of odonto‐differentiation between P75 ‐neurotrophin receptor (P75 ‐NTR)‐positive ectomesenchymal stem cells ( P 75 + EMSCs) and P75 ‐NTR‐negative ectomesenchymal stem cells ( P 75 − EMSCs), and their underlying mechanisms. Materials and methods: Primary cranial neural crest‐derived cells (CNC) were isolated from the first branchial arches, and P 75 + EMSCs and P 75 − EMSCs were sorted by fluorescence‐activated cell sorting. Differentiation of P 75 + EMSCs or P 75 − EMSCs into odontoblast‐like cells was induced by dental epithelial cells in vitro or in vivo . Differential gene expression profiles between P 75 + EMSCs and P 75 − EMSCs were analysed by microarray assay. Smad4‐specific small interfering RNA and activator kartogenin were used to treat the cells, to evaluate effects of Smad4 in odonto‐differentiation of P 75 + EMSCs or P 75 − EMSCs. Results: Under induction of dental epithelium conditioned medium, P 75 + EMSCs had more mineralized node formation and higher expression of Dmp1 and Dspp compared to P 75 − EMSCs. In our in vivo study, graft of P 75 + EMSCs recombination with dental epithelium showed higher expression of DMP1 and DSP. Knock‐down of Smad4 in P 75 + EMSCs significantly downregulated expression of DMP1 and DSP, while activation of Smad4 in P 75 − EMSCs by the activator kartogenin, significantly increased DSP and DMP1 expression. Conclusions: P 75 + EMSCs showed more odonto‐differentiation potential than P 75 − EMSCs both in vivo and in vitro . Smad4 played a critical role in determination of odonto‐differentiation potential of CNC‐derived EMSCs. … (more)
- Is Part Of:
- Cell proliferation. Volume 49:Number 2(2016:Apr.)
- Journal:
- Cell proliferation
- Issue:
- Volume 49:Number 2(2016:Apr.)
- Issue Display:
- Volume 49, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 49
- Issue:
- 2
- Issue Sort Value:
- 2016-0049-0002-0000
- Page Start:
- 185
- Page End:
- 194
- Publication Date:
- 2016-03-31
- Subjects:
- Cell proliferation -- Periodicals
571.84 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2184 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/cpr.12248 ↗
- Languages:
- English
- ISSNs:
- 0960-7722
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3097.854000
British Library DSC - BLDSS-3PM
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- 1248.xml