4.5 Article

Effects of Extracellular pH on Dental Pulp Cells In Vitro

期刊

JOURNAL OF ENDODONTICS
卷 42, 期 5, 页码 735-741

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.joen.2016.01.019

关键词

Cell death; dental pulp cells; extracellular pH; growth arrest; migration; proliferation

资金

  1. Budget for Promoting Science and Technology in Japan
  2. Research Grant for Longevity Sciences from the Ministry of Health, Labour and Welfare [23-10]
  3. Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan [26293422]
  4. Iwadare Educational Association for Dental Graduate Students
  5. Grants-in-Aid for Scientific Research [16K15787, 15H05012, 26293422, 26462779, 16H05847, 26462780] Funding Source: KAKEN

向作者/读者索取更多资源

Introduction: The proliferation and migration of dental pulp stem cells (DPSCs), a population comprised of dental pulp cells (DPCs), are important processes for pulp tissue repair. Dental pulp is exposed to changes in extracellular pH under various conditions, such as acidosis and exposure to caries-associated bacteria or a pulp capping agent. The objective of this study was to investigate the effects of extracellular pH on DPC proliferation and migration in vitro. Methods: To evaluate the proliferation potency of DPCs in various extracellular pH conditions, 2 x 10(4) cells were seeded into 35-mm dishes. The following day, we changed to NaHCO3-free medium, which was adjusted to different extracellular pH levels. Results: After 120 hours, DPCs cultured in media from a pH of 3.5 to 5.5 showed cell death, those cultured in conditions from a pH of 6.5 to 7.5 showed growth arrest or cell death, and those grown at a pH of 9.5 showed mild proliferation. The migratory activity of living DPCs was not affected by extracellular pH. For histologic analysis, human teeth possessing a small abscess in the corona] pulp chamber were sliced for histologic analysis. Proliferating cell nuclear antigen (PCNA) immunolocalization was used as an index of cell proliferation for the sections and cultured cells. Acidic extracellular pH conditions resulted in reduced numbers of PCNA-positive DPCs in the dishes. As for pulp tissue affected by a small abscess, a PCNA-negative pulp cell layer was observed in close proximity to the infectious lesion. Conclusions: Together, these results suggest that an acidic extracellular pH condition is associated with DPC growth arrest or cell death.

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