Combined effects of mineral trioxide aggregate and human placental extract on rat pulp tissue and growth, differentiation and angiogenesis in human dental pulp cells

Authors

  • Seok-Woo Chang Department of Conservative Dentistry
  • Ji-Youn Kim Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC)
  • Mi-Joo Kim Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC)
  • Ga-Hyun Kim Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC)
  • Jin-Kyu Yi Department of Conservative Dentistry
  • Deok-Won Lee Department of Oral and Maxillofacial Surgery School of Dentistry, Kyung Hee University, Seoul, Republic of Korea
  • Kee-Yeon Kum Department of Conservative Dentistry, Seoul National University Dental Hospital, Seoul, Republic of Korea
  • Eun-Cheol Kim Department of Oral and Maxillofacial Pathology and Research Center for Tooth and Periodontal Regeneration (MRC)

DOI:

https://doi.org/10.3109/00016357.2015.1120882

Keywords:

Angiogenesis, human dental pulp cells, human placental extract, MTA, odontogenic differentiation

Abstract

Objective The aim of this study was to evaluate the combined effects of mineral trioxide aggregate (MTA) and human placental extract (HPE) on cell growth, differentiation and in vitro angiogenesis of human dental pulp cells (HDPCs) and to identify underlying signal transduction mechanisms. In vivo dental pulp responses in rats for a pulp-capping agent were examined. Materials and methods MTS assay. ALP activity test, alizarin red S staining and RT-PCR for marker genes were carried out to evaluate cell growth and differentiation. HUVEC migration, mRNA expression and capillary tube formation were measured to evaluate angiogenesis. Signal transduction was analysed using Western blotting and confocal microscopy. The pulps of rat maxillary first molars were exposed and capped with either MTA or MTA plus HPE. Histologic observation and scoring were performed. Results Compared to treatment of HDPCs with either HPE or MTA alone, the combination of HPE and MTA increased cell growth, ALP activity, mineralized nodules and expression of marker mRNAs. Combination HPE and MTA increased migration, capillary tube formation and angiogenic gene expression compared with MTA alone. Activation of Akt, mammalian target of rapamycin (mTOR), p38, JNK and ERK MAPK, Akt, and NF-κB were significantly increased by combining HPE and MTA compared with MTA alone. Pulp capping with MTA plus HPE in rats showed superior dentin bridge formation, odontoblastic layers and dentinal tubules and lower inflammatory cell response, compared to the MTA alone group. Conclusions This study demonstrates for the first time that the use of MTA with HPE promotes cell growth, differentiation and angiogenesis in HDPCs, which were associated with mTOR, MAPK and NF-κB pathways. Direct pulp capping with HPE plus MTA showed superior results when compared with MTA alone. Thus, the combination of MTA and HPE may be useful for regenerative endodontics.

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Published

2016-05-18