Enterococcus faecalis Inhibits Osteoblast Differentiation and Induces Chemokine Expression

Abstract Introduction Enterococcus faecalis is commonly found in root canals of patients with refractory apical periodontitis, often accompanying inflammation and malfunctioning bone regeneration. In this study, we investigated the effect of E. faecalis on osteoblast differentiation and the ability...

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Veröffentlicht in:Journal of endodontics 2015-09, Vol.41 (9), p.1480-1485
Hauptverfasser: Park, Ok-Jin, PhD, Kim, Jiseon, MS, Yang, Jihyun, PhD, Yun, Cheol-Heui, PhD, Han, Seung Hyun, PhD
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container_end_page 1485
container_issue 9
container_start_page 1480
container_title Journal of endodontics
container_volume 41
creator Park, Ok-Jin, PhD
Kim, Jiseon, MS
Yang, Jihyun, PhD
Yun, Cheol-Heui, PhD
Han, Seung Hyun, PhD
description Abstract Introduction Enterococcus faecalis is commonly found in root canals of patients with refractory apical periodontitis, often accompanying inflammation and malfunctioning bone regeneration. In this study, we investigated the effect of E. faecalis on osteoblast differentiation and the ability to induce chemokine expression to recruit inflammatory cells. Methods Osteoblast precursors from mouse calvaria were differentiated into osteoblasts with ascorbic acid and β-glycerophosphate in the absence or presence of heat-killed E. faecalis (HKEF). Alizarin red S staining was performed to determine the degree of mineralization. Reporter gene and reverse-transcription polymerase chain reaction assays were performed to examine the activity of the Runx2 transcription factor and the expression of osteogenic marker genes, respectively. Secretion of the chemokines keratinocyte-derived chemokine and monocyte chemotactic protein-1 was measured by the enzyme-linked immunosorbent assay, and their functions were analyzed by measuring the migration of peripheral blood mononuclear cells using a transwell system. Results HKEF inhibited osteoblast mineralization and Runx2 transcriptional activity, which are typical features of osteoblast differentiation. HKEF also decreased the expression of Runx2, osterix, β-catenin, osteocalcin, and type I collagen. Interestingly, however, the expression of keratinocyte-derived chemokine and monocyte chemotactic protein-1 was increased by HKEF, and the culture supernatant of HKEF-stimulated osteoblasts increased the transmigration of peripheral blood mononuclear cells. Conclusions HKEF inhibits osteoblast differentiation and induces chemokine expression, which might be involved in refractory apical periodontitis and bone loss.
doi_str_mv 10.1016/j.joen.2015.04.025
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In this study, we investigated the effect of E. faecalis on osteoblast differentiation and the ability to induce chemokine expression to recruit inflammatory cells. Methods Osteoblast precursors from mouse calvaria were differentiated into osteoblasts with ascorbic acid and β-glycerophosphate in the absence or presence of heat-killed E. faecalis (HKEF). Alizarin red S staining was performed to determine the degree of mineralization. Reporter gene and reverse-transcription polymerase chain reaction assays were performed to examine the activity of the Runx2 transcription factor and the expression of osteogenic marker genes, respectively. Secretion of the chemokines keratinocyte-derived chemokine and monocyte chemotactic protein-1 was measured by the enzyme-linked immunosorbent assay, and their functions were analyzed by measuring the migration of peripheral blood mononuclear cells using a transwell system. Results HKEF inhibited osteoblast mineralization and Runx2 transcriptional activity, which are typical features of osteoblast differentiation. HKEF also decreased the expression of Runx2, osterix, β-catenin, osteocalcin, and type I collagen. Interestingly, however, the expression of keratinocyte-derived chemokine and monocyte chemotactic protein-1 was increased by HKEF, and the culture supernatant of HKEF-stimulated osteoblasts increased the transmigration of peripheral blood mononuclear cells. Conclusions HKEF inhibits osteoblast differentiation and induces chemokine expression, which might be involved in refractory apical periodontitis and bone loss.</description><identifier>ISSN: 0099-2399</identifier><identifier>EISSN: 1878-3554</identifier><identifier>DOI: 10.1016/j.joen.2015.04.025</identifier><identifier>PMID: 26141768</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Cell Differentiation ; Chemokine ; Chemokines - biosynthesis ; Core Binding Factor Alpha 1 Subunit - genetics ; Core Binding Factor Alpha 1 Subunit - metabolism ; Dental Pulp Cavity - cytology ; Dental Pulp Cavity - microbiology ; Dentistry ; Endocrinology &amp; Metabolism ; Enterococcus faecalis ; Enterococcus faecalis - physiology ; Mice ; Mice, Inbred C57BL ; osteoblast ; Osteoblasts - cytology ; Osteoblasts - metabolism ; Osteoblasts - microbiology ; Periapical Periodontitis - microbiology ; refractory apical periodontitis ; Runx2 ; Transcription, Genetic</subject><ispartof>Journal of endodontics, 2015-09, Vol.41 (9), p.1480-1485</ispartof><rights>American Association of Endodontists</rights><rights>2015 American Association of Endodontists</rights><rights>Copyright © 2015 American Association of Endodontists. Published by Elsevier Inc. 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In this study, we investigated the effect of E. faecalis on osteoblast differentiation and the ability to induce chemokine expression to recruit inflammatory cells. Methods Osteoblast precursors from mouse calvaria were differentiated into osteoblasts with ascorbic acid and β-glycerophosphate in the absence or presence of heat-killed E. faecalis (HKEF). Alizarin red S staining was performed to determine the degree of mineralization. Reporter gene and reverse-transcription polymerase chain reaction assays were performed to examine the activity of the Runx2 transcription factor and the expression of osteogenic marker genes, respectively. Secretion of the chemokines keratinocyte-derived chemokine and monocyte chemotactic protein-1 was measured by the enzyme-linked immunosorbent assay, and their functions were analyzed by measuring the migration of peripheral blood mononuclear cells using a transwell system. Results HKEF inhibited osteoblast mineralization and Runx2 transcriptional activity, which are typical features of osteoblast differentiation. HKEF also decreased the expression of Runx2, osterix, β-catenin, osteocalcin, and type I collagen. Interestingly, however, the expression of keratinocyte-derived chemokine and monocyte chemotactic protein-1 was increased by HKEF, and the culture supernatant of HKEF-stimulated osteoblasts increased the transmigration of peripheral blood mononuclear cells. Conclusions HKEF inhibits osteoblast differentiation and induces chemokine expression, which might be involved in refractory apical periodontitis and bone loss.</description><subject>Animals</subject><subject>Cell Differentiation</subject><subject>Chemokine</subject><subject>Chemokines - biosynthesis</subject><subject>Core Binding Factor Alpha 1 Subunit - genetics</subject><subject>Core Binding Factor Alpha 1 Subunit - metabolism</subject><subject>Dental Pulp Cavity - cytology</subject><subject>Dental Pulp Cavity - microbiology</subject><subject>Dentistry</subject><subject>Endocrinology &amp; Metabolism</subject><subject>Enterococcus faecalis</subject><subject>Enterococcus faecalis - physiology</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>osteoblast</subject><subject>Osteoblasts - cytology</subject><subject>Osteoblasts - metabolism</subject><subject>Osteoblasts - microbiology</subject><subject>Periapical Periodontitis - microbiology</subject><subject>refractory apical periodontitis</subject><subject>Runx2</subject><subject>Transcription, Genetic</subject><issn>0099-2399</issn><issn>1878-3554</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kbGO1DAURS0EYoeFH6BAKWkS7NiOHQkhoWGAlVbaAmhoLMd-0TqbsQc_B7F_T6JZKCioXnPuld65hLxktGGUdW-mZkoQm5Yy2VDR0FY-Ijumla65lOIx2VHa93XL-_6CPEOcKGWKc_WUXLQdE0x1eke-H2KBnFxybsFqtODsHLC6irdhCAWrGyyQhtliqT6EcYQMsQRbQoqVjX7l_OIAq_0tHNNdiFAdfp0yIK7Ac_JktDPCi4d7Sb59PHzdf66vbz5d7d9f105oVmrdWSm8AEm5pNpKphTvlPTKajF0A-1b3Q9Kj6MdXW8p52ClZ50duRfS24Ffktfn3lNOPxbAYo4BHcyzjZAWNExRrXvVdmJF2zPqckLMMJpTDkeb7w2jZnNqJrM5NZtTQ4VZna6hVw_9y3AE_zfyR-IKvD0DsH75M0A26AJEBz5kcMX4FP7f_-6fuJtDDOsQd3APOKUlx9WfYQZbQ82XbdVtVCYpFUJq_htgw53_</recordid><startdate>20150901</startdate><enddate>20150901</enddate><creator>Park, Ok-Jin, PhD</creator><creator>Kim, Jiseon, MS</creator><creator>Yang, Jihyun, PhD</creator><creator>Yun, Cheol-Heui, PhD</creator><creator>Han, Seung Hyun, PhD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150901</creationdate><title>Enterococcus faecalis Inhibits Osteoblast Differentiation and Induces Chemokine Expression</title><author>Park, Ok-Jin, PhD ; 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In this study, we investigated the effect of E. faecalis on osteoblast differentiation and the ability to induce chemokine expression to recruit inflammatory cells. Methods Osteoblast precursors from mouse calvaria were differentiated into osteoblasts with ascorbic acid and β-glycerophosphate in the absence or presence of heat-killed E. faecalis (HKEF). Alizarin red S staining was performed to determine the degree of mineralization. Reporter gene and reverse-transcription polymerase chain reaction assays were performed to examine the activity of the Runx2 transcription factor and the expression of osteogenic marker genes, respectively. Secretion of the chemokines keratinocyte-derived chemokine and monocyte chemotactic protein-1 was measured by the enzyme-linked immunosorbent assay, and their functions were analyzed by measuring the migration of peripheral blood mononuclear cells using a transwell system. 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subjects Animals
Cell Differentiation
Chemokine
Chemokines - biosynthesis
Core Binding Factor Alpha 1 Subunit - genetics
Core Binding Factor Alpha 1 Subunit - metabolism
Dental Pulp Cavity - cytology
Dental Pulp Cavity - microbiology
Dentistry
Endocrinology & Metabolism
Enterococcus faecalis
Enterococcus faecalis - physiology
Mice
Mice, Inbred C57BL
osteoblast
Osteoblasts - cytology
Osteoblasts - metabolism
Osteoblasts - microbiology
Periapical Periodontitis - microbiology
refractory apical periodontitis
Runx2
Transcription, Genetic
title Enterococcus faecalis Inhibits Osteoblast Differentiation and Induces Chemokine Expression
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