AI Article Synopsis

  • The study investigates the impact of the complement component C5a on the differentiation of dental pulp stem cells (DPSCs) under both normal (normoxic) and oxygen-deprived (hypoxic) conditions.
  • C5a was found to enhance the odontogenic differentiation of DPSCs in normoxia, while blocking the C5a receptor significantly reduced key differentiation genes.
  • Under hypoxic conditions, the positive effects of C5a on DPSC differentiation were reversed, highlighting the importance of C5a and oxygen levels in regulating stem cell behavior, which could inform treatments for dental repair.

Article Abstract

Aim: Alterations in the microenvironment change the phenotypes of dental pulp stem cells (DPSCs). The role of complement component C5a in the differentiation of DPSCs is unknown, especially under oxygen-deprived conditions. The aim of this study was to determine the effect of C5a on the odontogenic differentiation of DPSCs under normoxia and hypoxia.

Material And Methods: Human DPSCs were subjected to odontogenic differentiation in osteogenic media and treated with the C5a receptor antagonist-W54011 under normal and hypoxic conditions (2% oxygen). Immunochemistry, western blot, and PCR analysis for the various odontogenic differentiation genes/proteins were performed.

Results: Our results demonstrated that C5a plays a positive role in the odontogenic differentiation of DPSCs. C5a receptor inhibition resulted in a significant decrease in odontogenic differentiation genes, such as DMP1, ON, RUNX2, DSPP compared with the control. This observation was further supported by the Western blot data for DSPP and DMP1 and immunohistochemical analysis. The hypoxic condition reversed this effect.

Conclusions: Our results demonstrate that C5a regulates the odontogenic DPSC differentiation under normoxia. Under hypoxia, C5a exerts a reversed function for DPSC differentiation. Taken together, we identified that C5a and oxygen levels are key initial signals during pulp inflammation to control the odontogenic differentiation of DPSCs, thereby, providing a mechanism for potential therapeutic interventions for dentin repair and vital tooth preservation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8611100PMC
http://dx.doi.org/10.1080/03008207.2021.1924696DOI Listing

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