본문 바로가기
KERD
논문KCI 등재

Effects of Mineral Trioxide Aggregate on the Proliferation and Differentiation of Human Dental Pulp Stromal Cells from Permanent and Deciduous Teeth

2

조회

0

다운로드

1

인용

0

참고문헌

키워드

주제분류치의학

초록

Mineral trioxide aggregate (MTA) has recently been used as a pulpotomy medicament for primary molars. The aim of this study was to evaluate and compare the proliferation and differentiation potential of dental pulp stromal cells of permanent teeth and deciduous teeth cultured on MTA-coated surface. Human dental pulp stromal cells were obtained from human permanent premolars and deciduous teeth and cultured on MTA-coated culture plates. The cells were subjected to proliferation assay and cell cycle analysis. Their differentiation potential was evaluated by analysing changes in the mRNA expressions of runt-related transcriptional factor 2 (Runx2) and alkaline phosphatase (ALP). Morphological changes of cells in direct contact with MTA were observed using scanning electron microscopy (SEM). The proliferation rates, distribution of cell cycles and mRNA expression patterns of Runx2 and ALP were similar in both types of pulpal cells. SEM observations revealed that both types changed into more dendrite-like cells. On the surface of MTA, human dental pulp stromal cells from deciduous and permanent teeth were able to both proliferate and differentiate into cells that induce mineralization. MTA is suitable as a biocompatible pulpotomy medicament for primary teeth.

Abstract

Mineral trioxide aggregate (MTA) has recently been used as a pulpotomy medicament for primary molars. The aim of this study was to evaluate and compare the proliferation and differentiation potential of dental pulp stromal cells of permanent teeth and deciduous teeth cultured on MTA-coated surface. Human dental pulp stromal cells were obtained from human permanent premolars and deciduous teeth and cultured on MTA-coated culture plates. The cells were subjected to proliferation assay and cell cycle analysis. Their differentiation potential was evaluated by analysing changes in the mRNA expressions of runt-related transcriptional factor 2 (Runx2) and alkaline phosphatase (ALP). Morphological changes of cells in direct contact with MTA were observed using scanning electron microscopy (SEM). The proliferation rates, distribution of cell cycles and mRNA expression patterns of Runx2 and ALP were similar in both types of pulpal cells. SEM observations revealed that both types changed into more dendrite-like cells. On the surface of MTA, human dental pulp stromal cells from deciduous and permanent teeth were able to both proliferate and differentiate into cells that induce mineralization. MTA is suitable as a biocompatible pulpotomy medicament for primary teeth.

참고문헌 (32)

  1. Judd PL, "Formocresol concerns. A review", J Can Dent Assoc, 53, pp.401~404 (1987)
  2. International Agency for Research on Cancer, "IARC classifies formaldehyde as carcinogenic to humans. Press release no. 153", World Health Organization International Agency for research on Cancer, ~ (2004)
  3. Deery C, "Formocresol and ferric sulfate have similar success rates in primary molar pulpotomy. In carious primary molars does a pulpotomy performed with ferric sulphate, compared with formocresol, result in greater clinical", radiographic success?, 2005, pp.6, 70~
  4. Fei AL, "A clinical study of fer ric sulfate as a pulpotomy agent in primary teeth", Pediatr Dent, 13, pp.327~332 (1991)
  5. Loh A, "Evidence-based assessment: evaluation of the formocresol versus ferric sulfate primary molar pulpotomy", Pediatr Dent, 26, pp.401~409 (2004)
  6. Shayegan A, "Beta-tricalcium phosphate, white mineral trioxide aggregate, white Portland cement, ferric sulfate, and formocresol used as pulpotomy agents in primary pig teeth", Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 105, pp.536~542 (2008)
  7. Peng L, "Evaluation of the formocresol versus mineral trioxide aggregate primary molar pulpotomy: a meta-analysis", Oral Surg Oral Med Oral Pathol Oral Radiol Endod, 102, pp.40~44 (2006)
  8. Noorollahian H, "Comparison of mineral trioxide aggregate and formocresol as pulp medicaments for pulpotomies in primary molars", Br Dent J, 204, pp.20~ (2008)
  9. Torabinejad M, "Sealing ability of a mineral trioxide aggregate when used as a root end filling material", J Endod, 19, pp.591~595 (1993)
  10. Salako N, "Comparison of bioactive glass, mineral trioxide aggregate, ferric sulfate, and formocresol as pulpotomy agents in rat molar", Dent Traumatol, 19, pp.314~320 (2003)
  11. Min KS, "The combined effect of mineral trioxide aggregate and enamel matrix derivative on odontoblastic differentiation in human dental pulp cells", J Endod, 35, pp.847~851 (2009)
  12. Paranjpe A, "Nacetyl cysteine mediates protection from 2-hydroxyethyl methacrylate induced apoptosis via nuclear factor kappa B-dependent and independent pathways: potential involvement of JNK", Toxicol Sci, 108, pp.356~366 (2009)
  13. Takita T, "Effect of mineral trioxide aggregate on proliferation of cultured human dental pulp cells", Int Endod J, 39, pp.415~422 (2006)
  14. Wang MY, "Effects of mineral trioxide aggregate and calcium hydroxide on the proliferation and differentiation capacity of pulp cells of primary teeth", Zhonghua Kou Qiang Yi Xue Za Zhi, 43, pp.524~527 (2008)
  15. Miura M, "SHED: stem cells from human exfoliated deciduous teeth", Proc Natl Acad Sci U S A, 100, pp.5807~5812 (2003)
  16. Gronthos S, "Stem cell properties of human dental pulp stem cells", J Dent Res, 81, pp.531~535 (2002)
  17. Gronthos S, "Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo", Proc Natl Acad Sci U S A, 97, pp.13625~13630 (2000)
  18. Nakamura S, "Stem cell proliferation pathways comparison between human exfoliated deciduous teeth and dental pulp stem cells by gene expression profile from promising dental pulp", J Endod, 35, pp.1536~1542 (2009)
  19. Torabinejad M, "Mineral trioxide aggregate: a comprehensive literature review--part II: leakage and biocompatibility investigations", J Endod, 36, pp.190~202 (2010)
  20. Camilleri J, "Mineral trioxide aggregate: a review of the constituents and biological properties of the material", Int Endod J, 39, pp.747~754 (2006)
  21. 최유석, "Mineral Trioxide Aggregate(MTA)에 의한 치수세포의 유전자 발현변화", 대한소아치과학회지, 35(1), pp.30~38 (2008), 대한소아치과학회
  22. Moghaddame-Jafari S, "Effect of ProRoot MTA on pulp cell apoptosis and proliferation in vitro", J Endod, 31, pp.387~391 (2005)
  23. Ford TR, "Using mineral trioxide aggregate as a pulp-capping material", J Am Dent Assoc, 127, pp.1491~1494 (1996)
  24. Faraco IM, Jr., "Response of the pulp of dogs to capping with mineral trioxide aggregate or a calcium hydroxide cement", Dent Traumatol, 17, pp.163~166 (2001)
  25. Accorinte ML, "Response of human dental pulp capped with MTA and calcium hydroxide powder", Oper Dent, 33, pp.488~495 (2008)
  26. Moretti AB, "The effectiveness of mineral trioxide aggregate, calcium hydroxide and formocresol for pulpotomies in primary teeth", Int Endod J, 41, pp.547~555 (2008)
  27. Yasuda Y, "The effect of mineral trioxide aggregate on the mineralization ability of rat dental pulp cells: an in vitro study", J Endod, 34, pp.1057~1060 (2008)
  28. Ducy P, "A Cbfa1- dependent genetic pathway controls bone formation beyond embryonic development", Genes Dev, 13, pp.1025~1036 (1999)
  29. Chen S, "Differential regulation of dentin sialophosphoprotein expression by Runx2 during odontoblast cytodifferentiation", J Biol Chem, 280, pp.29717~29727 (2005)
  30. Mizuno M, "Bone sialoprotein (BSP) is a crucial factor for the expression of osteoblastic phenotypes of bone marrow cells cultured on type I collagen matrix", Calcif Tissue Int, 66, pp.388~396 (2000)
  31. Butler WT, "Dentin matrix proteins and dentinogenesis", Connect Tissue Res, 33, pp.59~65 (1995)
  32. Lian JB, "Concepts of osteoblast growth and differentiation: basis for modulation of bone cell development and tissue formation", Crit Rev Oral Biol Med, 3, pp.269~305 (1992)

관련 논문AI추천

이 간행물의 다른 논문 (9건)