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Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines

OBJECTIVE: Regulation of immune-like cell properties of periodontal ligament (PDL) cells is not understood. We investigate the importance of secretory leukocyte protease inhibitor (SLPI) for production of pro-inflammatory cytokines in human PDL cells. MATERIALS AND METHODS: PDL cells were isolated f...

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Autores principales: Svensson, Daniel, Aidoukovitch, Alexandra, Anders, Emma, Jönsson, Daniel, Nebel, Daniel, Nilsson, Bengt-Olof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529494/
https://www.ncbi.nlm.nih.gov/pubmed/28597116
http://dx.doi.org/10.1007/s00011-017-1062-2
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author Svensson, Daniel
Aidoukovitch, Alexandra
Anders, Emma
Jönsson, Daniel
Nebel, Daniel
Nilsson, Bengt-Olof
author_facet Svensson, Daniel
Aidoukovitch, Alexandra
Anders, Emma
Jönsson, Daniel
Nebel, Daniel
Nilsson, Bengt-Olof
author_sort Svensson, Daniel
collection PubMed
description OBJECTIVE: Regulation of immune-like cell properties of periodontal ligament (PDL) cells is not understood. We investigate the importance of secretory leukocyte protease inhibitor (SLPI) for production of pro-inflammatory cytokines in human PDL cells. MATERIALS AND METHODS: PDL cells were isolated from teeth extracted for orthodontic reasons. Cellular location of SLPI was investigated by immunocytochemistry. Cytokine transcript and protein expression were assessed by quantitative real-time RT-PCR and Western blotting. SLPI gene activity was knocked-down by siRNA. NF-κB signaling was assessed by measuring IκBα, and phosphorylated p65 and p105 protein expression. RESULTS: PDL cells showed cytoplasmic expression of SLPI. Cellular expression level of SLPI negatively correlated to LPS-induced stimulation of IL-6 and MCP-1. Both SLPI gene activity and protein were reduced by about 70% in PDL cells treated with SLPI siRNA compared to cells treated with non-coding construct. Treatment with SLPI siRNA was associated with up-regulation of both basal and LPS-stimulated IL-6, MCP-1 and TLRs mRNA expression. The up-regulation of MCP-1 transcript in SLPI siRNA-treated cells was confirmed on protein level. SLPI siRNA-treatment enhanced the phosphorylated NF-κB p105 protein expression. CONCLUSIONS: SLPI regulates PDL cell pro-inflammatory cytokine expression and modulates NF-κB signaling, suggesting that SLPI governs the immune cell-like properties of PDL cells.
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spelling pubmed-55294942017-08-08 Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines Svensson, Daniel Aidoukovitch, Alexandra Anders, Emma Jönsson, Daniel Nebel, Daniel Nilsson, Bengt-Olof Inflamm Res Original Research Paper OBJECTIVE: Regulation of immune-like cell properties of periodontal ligament (PDL) cells is not understood. We investigate the importance of secretory leukocyte protease inhibitor (SLPI) for production of pro-inflammatory cytokines in human PDL cells. MATERIALS AND METHODS: PDL cells were isolated from teeth extracted for orthodontic reasons. Cellular location of SLPI was investigated by immunocytochemistry. Cytokine transcript and protein expression were assessed by quantitative real-time RT-PCR and Western blotting. SLPI gene activity was knocked-down by siRNA. NF-κB signaling was assessed by measuring IκBα, and phosphorylated p65 and p105 protein expression. RESULTS: PDL cells showed cytoplasmic expression of SLPI. Cellular expression level of SLPI negatively correlated to LPS-induced stimulation of IL-6 and MCP-1. Both SLPI gene activity and protein were reduced by about 70% in PDL cells treated with SLPI siRNA compared to cells treated with non-coding construct. Treatment with SLPI siRNA was associated with up-regulation of both basal and LPS-stimulated IL-6, MCP-1 and TLRs mRNA expression. The up-regulation of MCP-1 transcript in SLPI siRNA-treated cells was confirmed on protein level. SLPI siRNA-treatment enhanced the phosphorylated NF-κB p105 protein expression. CONCLUSIONS: SLPI regulates PDL cell pro-inflammatory cytokine expression and modulates NF-κB signaling, suggesting that SLPI governs the immune cell-like properties of PDL cells. Springer International Publishing 2017-06-08 2017 /pmc/articles/PMC5529494/ /pubmed/28597116 http://dx.doi.org/10.1007/s00011-017-1062-2 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Research Paper
Svensson, Daniel
Aidoukovitch, Alexandra
Anders, Emma
Jönsson, Daniel
Nebel, Daniel
Nilsson, Bengt-Olof
Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
title Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
title_full Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
title_fullStr Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
title_full_unstemmed Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
title_short Secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
title_sort secretory leukocyte protease inhibitor regulates human periodontal ligament cell production of pro-inflammatory cytokines
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5529494/
https://www.ncbi.nlm.nih.gov/pubmed/28597116
http://dx.doi.org/10.1007/s00011-017-1062-2
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