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(Reference retrieved automatically from SciELO through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Immunomodulatory effects of apical papilla cells on periodontal ligament fibroblasts stimulated with Escherichia coli lipopolysaccharide: an in vitro study

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Author(s):
Alexandre Guimarães dos SANTOS [1] ; Karollyne Santos SPIGARIOL [2] ; Letícia Martins SANTOS [3] ; Marinella HOLZHAUSEN [4] ; Carla Renata SIPERT [5]
Total Authors: 5
Affiliation:
[1] Universidade de São Paulo. Faculdade de Odontologia. Departamento de Dentística - Brasil
[2] Universidade de São Paulo. Faculdade de Odontologia. Departamento de Dentística - Brasil
[3] Universidade de São Paulo. Faculdade de Odontologia. Departamento de Biomateriais e Biologia Oral - Brasil
[4] Universidade de São Paulo. Faculdade de Odontologia. Departamento de Estomatologia - Brasil
[5] Universidade de São Paulo. Faculdade de Odontologia. Departamento de Dentística - Brasil
Total Affiliations: 5
Document type: Journal article
Source: Journal of Applied Oral Science; v. 33, 2025-03-14.
Abstract

Abstract The role of human Stem Cells from the Apical Papilla (SCAP) in tissue regeneration has been described, but their impact on modulating the apical inflammatory process by other surrounding cell populations, such as periodontal ligament fibroblasts (PLFs), is unclear. Therefore, we investigated the role of SCAP in the activation of PLFs in vitro. Methods Primary SCAP culture was used to obtain conditioned media (CM). A primary human PLF culture was established and stimulated with increasing concentrations of Escherichia coli lipopolysaccharide (LPS) (0.01, 0.1, and 1 µg/mL). At the 24 h time-point, an MTT viability assay was performed, and interleukin (IL)-6 and chemokine (CC-motif) ligand 2 (CCL2) levels were quantified by enzyme-linked immunosorbent assay. Then, PLFs were stimulated with LPS in the presence of SCAP-CM (1:5 dilution) for cell viability assessment and cytokine detection. The following groups were tested: PLF activated with LPS at concentrations of 0.01 and 1 µg/mL with or without SCAP-CM; a group with PLF stimulated by SCAP-CM alone; and a control group (proliferation medium only). The experiments were conducted in triplicate and sextuplicate. Statistical analyses were performed using analysis of variance followed by Tukey’s post-hoc test, with statistical significance established at 5% (p=0.05). Results The MTT assay showed no cytotoxicity of LPS or SCAP-CM on PLFs (p>0.05). The production of CCL2 and IL-6 significantly increased in the presence of SCAP-CM regardless of the presence of LPS (p<0.0001). Conclusion SCAP-CM significantly enhanced the release of proinflammatory cytokines by PLFs in vitro. (AU)

FAPESP's process: 20/12726-0 - Role of osteoprotegerin on in vitro modulation of monocytes by apical papilla cells
Grantee:Carla Renata Sipert
Support Opportunities: Regular Research Grants
FAPESP's process: 22/14686-0 - Role of osteoprotegerin on in vitro modulation of monocytes by apical papilla cells
Grantee:Letícia Martins Santos
Support Opportunities: Scholarships in Brazil - Doctorate