Insulin-like growth factor 1 promotes the proliferation and committed differentiation of human dental pulp stem cells through MAPK pathways. (December 2016)
- Record Type:
- Journal Article
- Title:
- Insulin-like growth factor 1 promotes the proliferation and committed differentiation of human dental pulp stem cells through MAPK pathways. (December 2016)
- Main Title:
- Insulin-like growth factor 1 promotes the proliferation and committed differentiation of human dental pulp stem cells through MAPK pathways
- Authors:
- Lv, Taohong
Wu, Yongzheng
Mu, Chao
Liu, Genxia
Yan, Ming
Xu, Xiangqin
Wu, Huayin
Du, Jinyin
Yu, Jinhua
Mu, Jinquan - Abstract:
- Highlights: IGF-1 can up-regulate the ALP activity and mineralization capacity of hDPSCs. MAPK signaling pathway is activated during the differentiation of hDPSCs. IGF-1 promotes the proliferation and osteogenic/odontogenic differentiation of hDPSCs. Abstract: Objectives: Insulin-like growth factor 1 (IGF-1) is a broad-spectrum growth-promoting factor that plays a key role in natural tooth development. Human dental pulp stem cells (hDPSCs) are multipotent and can influence the reparative regeneration of dental pulp and dentin. This study was designed to evaluate the effects of IGF-1 on the proliferation and differentiation of human dental pulp stem cells. Methods: HDPSCs were isolated and purified from human dental pulps. The proliferation and osteo/odontogenic differentiation of hDPSCs treated with 100 ng/ml exogenous IGF-1 were subsequently investigated. Results: MTT assays revealed that IGF-1 enhanced the proliferation of hDPSCs. ALP activity in IGF-1-treated group was obviously enhanced compared to the control group from days 3 to 9. Alizarin red staining revealed that the IGF-1-treated cells contained a greater number of mineralization nodules and had higher calcium concentrations. Moreover, western blot and qRT-PCR analyses demonstrated that the expression levels of several osteogenic genes (e.g., RUNX2, OSX, and OCN) and an odontoblast-specific marker (DSPP) were significantly up-regulated in IGF-1-treated hDPSCs as compared with untreated cells (P < 0.01).Highlights: IGF-1 can up-regulate the ALP activity and mineralization capacity of hDPSCs. MAPK signaling pathway is activated during the differentiation of hDPSCs. IGF-1 promotes the proliferation and osteogenic/odontogenic differentiation of hDPSCs. Abstract: Objectives: Insulin-like growth factor 1 (IGF-1) is a broad-spectrum growth-promoting factor that plays a key role in natural tooth development. Human dental pulp stem cells (hDPSCs) are multipotent and can influence the reparative regeneration of dental pulp and dentin. This study was designed to evaluate the effects of IGF-1 on the proliferation and differentiation of human dental pulp stem cells. Methods: HDPSCs were isolated and purified from human dental pulps. The proliferation and osteo/odontogenic differentiation of hDPSCs treated with 100 ng/ml exogenous IGF-1 were subsequently investigated. Results: MTT assays revealed that IGF-1 enhanced the proliferation of hDPSCs. ALP activity in IGF-1-treated group was obviously enhanced compared to the control group from days 3 to 9. Alizarin red staining revealed that the IGF-1-treated cells contained a greater number of mineralization nodules and had higher calcium concentrations. Moreover, western blot and qRT-PCR analyses demonstrated that the expression levels of several osteogenic genes (e.g., RUNX2, OSX, and OCN) and an odontoblast-specific marker (DSPP) were significantly up-regulated in IGF-1-treated hDPSCs as compared with untreated cells (P < 0.01). Interestingly, the expression of phospho-ERK and phospho-p38 were also up-regulated, indicating that the MAPK signaling pathway is activated during the differentiation of hDPSCs. Conclusions: IGF-1 can promote the proliferation and osteo/odontogenic differentiation of hDPSCs by activating MAPK pathways. … (more)
- Is Part Of:
- Archives of oral biology. Volume 72(2016)
- Journal:
- Archives of oral biology
- Issue:
- Volume 72(2016)
- Issue Display:
- Volume 72, Issue 2016 (2016)
- Year:
- 2016
- Volume:
- 72
- Issue:
- 2016
- Issue Sort Value:
- 2016-0072-2016-0000
- Page Start:
- 116
- Page End:
- 123
- Publication Date:
- 2016-12
- Subjects:
- ALP alkaline phosphatase -- a-MEM a-minimum essential medium -- BMPs bone morphogenetic proteins -- CPC cetyl pyridinium chloride -- DSP dentin sialoprotein -- DSPP dentin sialophosphoprotein -- ERK extracellular regulated protein kinases -- FBS fetal bovine serum -- FGFs fibroblast growth factors -- GAPDH glyceraldehyde-3-phosphate dehydrogenase -- HDPSCs human dental pulp stem cells -- IGF-1 insulin-like growth factor 1 -- IGFs insulin-like growth factors -- JNK c-Jun N-terminal kinase -- MAPK mitogen-activated protein kinase -- MTT 3-[4, 5-dimethylthiazol-2-yl]-2, 5-diphenyltetrazolium bromide -- OCN osteocalcin -- OD optical density -- OSX osterix -- PBS phosphate buffered saline -- PDGFs platelet-derived growth factors -- qRT-PCR quantitative reverse transcription polymerase chain reaction -- RUNX2 runt-related transcription factor2 -- TGFs transforming growth factors
Insulin-like growth factor 1 -- Dental pulp stem cells -- Osteogenesis -- Odontogenesis -- Proliferation -- Differentiation
Mouth -- Periodicals
Mouth -- Diseases -- Periodicals
Dentistry -- Periodicals
Electronic journals
617.6005 - Journal URLs:
- http://www.elsevier.com/journals ↗
- DOI:
- 10.1016/j.archoralbio.2016.08.011 ↗
- Languages:
- English
- ISSNs:
- 0003-9969
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1638.475000
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