CCL3 and CXCL12 production in vitro by dental pulp fibroblasts from permanent and deciduous teeth stimulated by Porphyromonas gingivalis LPS
- Carla Renata Sipert,
- ,
- Karin Cristina da Silva Modena,
- Thiago Jose Dionisio,
- Maria Aparecida Andrade Moreira Machado,
- Sandra Helena Penha de Oliveira
- Universidade de São Paulo,
- Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo,
- Universidade Estadual Paulista Júlio de Mesquita Filho
Open access
Abstract
Objective: The aim of this study was to compare the production of the chemokines CCL3 and CXCL12 by cultured dental pulp fibroblasts from permanent (PDPF) and deciduous (DDPF) teeth under stimulation by Porphyromonas gingivalis LPS (PgLPS). Material and Methods: Primary culture of fibroblasts from permanent (n=3) and deciduous (n=2) teeth were established using an explant technique. After the fourth passage, fibroblasts were stimulated by increasing concentrations of PgLPS (0 - 10 pg/mL) at 1, 6 and 24 h. The cells were tested for viability through MTT assay, and production of the chemokines CCL3 and CXCL12 was determined through ELISA. Comparisons among samples were performed using One-way ANOVA for MTT assay and Two-way ANOVA for ELISA results. Results: Cell viability was not affected by the antigen after 24 h of stimulation. PgLPS induced the production of CCL3 by dental pulp fibroblasts at similar levels for both permanent and deciduous pulp fibroblasts. Production of CXCL12, however, was significantly higher for PDPF than DDPF at 1 and 6 h. PgLPS, in turn, downregulated the production of CXCL12 by PDPF but not by DDPF. Conclusion: These data suggest that dental pulp fibroblasts from permanent and deciduous teeth may present a differential behavior under PgLPS stimulation.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 99-105 (7 pages)Journal (Volume, Issue Number)
Journal of Applied Oral Science (Volume 21, Issue 2)Publication milestones
- Published - 2013
Publication status
ISSN
1678-7757Publication IDs
- Scopus: 84878168654
- PubMed: 23739851
- ORCID: /0000-0003-4749-571X/work/107901297
