Role of the p38 pathway in mineral trioxide aggregate-induced cell viability and angiogenesis-related proteins of dental pulp cell in vitro

doi:10.1111/iej.12305

中山醫學大學機構典藏 CSMUIR > 口腔醫學院 > 牙醫學系暨碩士班 > 期刊論文 > Item 310902500/18229

Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/18229

Title:	Role of the p38 pathway in mineral trioxide aggregate-induced cell viability and angiogenesis-related proteins of dental pulp cell in vitro
Authors:	Huang, S.-C.;Wu, B.-C.;Kao, C.-T.;Huang, T.-H.;Hung, C.-J.;Shie, M.-Y.
Keywords:	Angiogenesis;Human dental pulp cell;Mineral trioxide aggregate;Osmolality;P38/MAPK
Date:	2015
Issue Date:	2017-08-09T04:42:23Z (UTC)
Publisher:	Blackwell Publishing Ltd
ISSN:	1432885
Abstract:	Aim: To investigate the influence of mineral trioxide aggregate (MTA) on angiogenesis of primary human dental pulp cells (hDPCs) via the MAPK pathway, in particular p38. Methodology: Human dental pulp cells were cultured with MTA to angiogenesis, after which cell viability, ion concentration, osmolality, NO secretion, the von Willebrand factor (vWF) and angiopoietin-1 (Ang-1) protein expression were examined. PrestoBlue® was used for evaluating the proliferation of hDPCs. An enzyme-linked immunosorbent assay was employed to determine vWF and Ang-1 protein secretion in hDPCs cultured on MTA and the control. Cells cultured on the tissue culture plate without the cement were used as the control. The t-test was used to evaluate the significance of the differences between the mean values. Results: Mineral trioxide aggregate elicited a significant (P < 0.05) increased viability compared with the control (15%, 16% and 13% on days 1, 3 and 5 of cell seeding, respectively). MTA consumed calcium and phosphate ions, and released more Si ions in the medium. MTA significantly (P < 0.05) increased the osmolality of the medium to 313, 328 and 341 mOsm kg-1 after 1, 3 and 5 days, respectively. P38 was activated through phosphorylation, and the phosphorylation kinase was investigated in the cell system after being cultured with MTA. Expression levels for Ang-1 and vWF in hDPCs on MTA were higher than those of the MTA + p38 inhibitor (SB203580) group (P < 0.05) at all of the time-points. Conclusions: Mineral trioxide aggregate was able to activate the p38 pathway in hDPCs cultured in vitro. Moreover, Si increased the osmolality required to facilitate the angiogenic differentiation of hDPCs via the p38 signalling pathway. When the p38 pathway was blocked by SB203580, the angiogenic-dependent protein secretion decreased. These findings verify that the p38 pathway plays a key role in regulating the angiogenic behaviour of hDPCs cultured on MTA. © 2014 International Endodontic Journal.
URI:	http://dx.doi.org/10.1111/iej.12305 https://www.scopus.com/inward/record.uri?eid=2-s2.0-84923108162&doi=10.1111%2fiej.12305&partnerID=40&md5=81a8d67722d413f0ae6d96f4ac981d0c https://ir.csmu.edu.tw:8080/ir/handle/310902500/18229
Relation:	International Endodontic Journal 48(3) ,236-245
Appears in Collections:	[牙醫學系暨碩士班] 期刊論文

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