An in vitro coculture approach to study the interplay between dental pulp cells and Streptococcus mutans

Author:

Akamp Tobias1,Rosendahl Andreas1,Galler Kerstin M.2,Wölflick Melanie1,Buchalla Wolfgang1,Widbiller Matthias1ORCID

Affiliation:

1. Department of Conservative Dentistry and Periodontology University Hospital Regensburg Regensburg Germany

2. Department of Operative Dentistry and Periodontology Friedrich‐Alexander‐University Erlangen‐Nürnberg Erlangen Germany

Abstract

AbstractAimTo develop a new coculture system that allows exposure of dental pulp cells (DPCs) to Streptococcus mutans and dentine matrix proteins (eDMP) to study cellular interactions in dentine caries.MethodologyDental pulp cells and S. mutans were cocultured with or without eDMP for 72 h. Cell proliferation and viability were assessed by cell counting and MTT assays, while bacterial growth and viability were determined by CFU and LIVE/DEAD staining. Glucose catabolism and lactate excretion were measured photometrically as metabolic indicators. To evaluate the inflammatory response, the release of cytokines and growth factors (IL‐6, IL‐8, TGF‐β1, VEGF) was determined by ELISA. Non‐parametric statistical analyses were performed to compare all groups and time points (Mann–Whitney U test or Kruskal–Wallis test; α = .05).ResultsWhile eDMP and especially S. mutans reduced the number and viability of DPCs (p ≤ .0462), neither DPCs nor eDMP affected the growth and viability of S. mutans during coculture (p > .0546). The growth of S. mutans followed a common curve, but the death phase was not reached within 72 h. S. mutans consumed medium glucose in only 30 h, whereas in the absence of S. mutans, cells were able to catabolize glucose throughout 72 h, resulting in the corresponding amount of l‐lactate. No change in medium pH was observed. S. mutans induced IL‐6 production in DPCs (p ≤ .0011), whereas eDMP had no discernible effect (p > .7509). No significant changes in IL‐8 were observed (p > .198). TGF‐β1, available from eDMP supplementation, was reduced by DPCs over time. VEGF, on the other hand, was increased in all groups during coculture.ConclusionsThe results show that the coculture of DPCs and S. mutans is possible without functional impairment. The bacterially induced stimulation of proinflammatory and regenerative cytokines provides a basis for future investigations and the elucidation of molecular biological relationships in pulp defence against caries.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Dentistry

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