The presence of neutrophils causes RANKL expression in periodontal tissue, giving rise to osteoclast formation
Backgrounds and Objective Increased neutrophil infiltration and osteoclast formation are key characteristics of periodontitis. The effect of these neutrophils on osteoclast formation in periodontitis remains unclear. Therefore, we investigated the effects of neutrophils on osteoclast formation in a...
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Veröffentlicht in: | Journal of periodontal research 2020-12, Vol.55 (6), p.868-876 |
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creator | Kim, Ae Ri Kim, Ji‑Hye Choi, Yun Hui Jeon, Yeong‐Eui Cha, Jeong‑Heon Bak, Eun‑Jung Yoo, Yun‑Jung |
description | Backgrounds and Objective
Increased neutrophil infiltration and osteoclast formation are key characteristics of periodontitis. The effect of these neutrophils on osteoclast formation in periodontitis remains unclear. Therefore, we investigated the effects of neutrophils on osteoclast formation in a neutrophil‐deficient mouse model of periodontitis.
Methods
Anti‐Ly6G antibody (Ab) was used for neutrophil depletion in two mouse models: periodontitis and air pouch. In the periodontitis experiments, mice were divided into PBS‐administered control (C), control Ab‐administered periodontitis (P), and anti‐Ly6G Ab‐administered periodontitis (P + Ly6G) groups. Periodontitis was induced by ligature of mandibular first molars. In the air pouch experiments, mice were divided into PBS‐administered (C), LPS and control Ab‐administered (LPS), and LPS and anti‐Ly6G Ab‐administered (LPS + Ly6G) groups. Neutrophil migration into air pouches was induced by LPS injection. Flow cytometry was used to examine CD11b+Ly6G+ neutrophils in the blood of periodontitis mice and CD11b+Ly6G+RANKL+ neutrophils in exudates of air pouch mice. In periodontal tissue, Ly6G+ neutrophil and RANKL+ cell numbers in periodontal ligament and alveolar bone areas were estimated using immunohistochemistry, osteoclast numbers were measured using TRAP assay, and alveolar bone loss was determined by H&E staining.
Results
In blood, CD11b+Ly6G+ neutrophils were found in greater percentage in the P group than in the C group on days 3 and 7. However, the percentage of neutrophils was lower in the P + Ly6G group than in the C and P groups. In periodontal tissue, the numbers of Ly6G+ neutrophils and RANKL+ cells were lower in the P + Ly6G group than in the P group on day 3. Ly6G+ neutrophil numbers decreased more in the P + Ly6G group than in the P group on day 7, but RANKL+ cell numbers did not decrease in the P + Ly6G group. In exudates, the number of CD11b+Ly6G+RANKL+ neutrophils was greater in the LPS group than in the C and LPS + Ly6G groups. On days 3 and 7, the numbers of osteoclasts and alveolar bone loss were greater in periodontal tissue in the P and P + Ly6G groups than in the C group. Interestingly, there were fewer osteoclasts in the P + Ly6G group than in the P group on day 3.
Conclusion
Neutrophil deficiency caused a reduction in numbers of both RANKL+ cells and osteoclasts in periodontitis‐induced tissues only on day 3. Furthermore, in the LPS‐injected air pouch model, neutrophil deficiency redu |
doi_str_mv | 10.1111/jre.12779 |
format | Article |
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Increased neutrophil infiltration and osteoclast formation are key characteristics of periodontitis. The effect of these neutrophils on osteoclast formation in periodontitis remains unclear. Therefore, we investigated the effects of neutrophils on osteoclast formation in a neutrophil‐deficient mouse model of periodontitis.
Methods
Anti‐Ly6G antibody (Ab) was used for neutrophil depletion in two mouse models: periodontitis and air pouch. In the periodontitis experiments, mice were divided into PBS‐administered control (C), control Ab‐administered periodontitis (P), and anti‐Ly6G Ab‐administered periodontitis (P + Ly6G) groups. Periodontitis was induced by ligature of mandibular first molars. In the air pouch experiments, mice were divided into PBS‐administered (C), LPS and control Ab‐administered (LPS), and LPS and anti‐Ly6G Ab‐administered (LPS + Ly6G) groups. Neutrophil migration into air pouches was induced by LPS injection. Flow cytometry was used to examine CD11b+Ly6G+ neutrophils in the blood of periodontitis mice and CD11b+Ly6G+RANKL+ neutrophils in exudates of air pouch mice. In periodontal tissue, Ly6G+ neutrophil and RANKL+ cell numbers in periodontal ligament and alveolar bone areas were estimated using immunohistochemistry, osteoclast numbers were measured using TRAP assay, and alveolar bone loss was determined by H&E staining.
Results
In blood, CD11b+Ly6G+ neutrophils were found in greater percentage in the P group than in the C group on days 3 and 7. However, the percentage of neutrophils was lower in the P + Ly6G group than in the C and P groups. In periodontal tissue, the numbers of Ly6G+ neutrophils and RANKL+ cells were lower in the P + Ly6G group than in the P group on day 3. Ly6G+ neutrophil numbers decreased more in the P + Ly6G group than in the P group on day 7, but RANKL+ cell numbers did not decrease in the P + Ly6G group. In exudates, the number of CD11b+Ly6G+RANKL+ neutrophils was greater in the LPS group than in the C and LPS + Ly6G groups. On days 3 and 7, the numbers of osteoclasts and alveolar bone loss were greater in periodontal tissue in the P and P + Ly6G groups than in the C group. Interestingly, there were fewer osteoclasts in the P + Ly6G group than in the P group on day 3.
Conclusion
Neutrophil deficiency caused a reduction in numbers of both RANKL+ cells and osteoclasts in periodontitis‐induced tissues only on day 3. Furthermore, in the LPS‐injected air pouch model, neutrophil deficiency reduced the influx of RANKL+ neutrophils. These findings suggest that the presence of neutrophils induces RANKL expression and could induce osteoclast formation in the early stages of periodontitis.</description><identifier>ISSN: 0022-3484</identifier><identifier>EISSN: 1600-0765</identifier><identifier>DOI: 10.1111/jre.12779</identifier><identifier>PMID: 32583887</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Alveolar bone ; Alveolar Bone Loss ; Animal models ; Animals ; Bone loss ; CD11b antigen ; Exudates ; Flow cytometry ; Gum disease ; Immunohistochemistry ; Leukocyte migration ; Leukocytes (neutrophilic) ; Lipopolysaccharides ; Mice ; Molars ; Neutrophils ; Neutrophils - physiology ; Osteoclasts ; Periodontal ligament ; Periodontitis ; Periodontium ; RANK Ligand - metabolism ; RANKL ; Teeth ; TRANCE protein</subject><ispartof>Journal of periodontal research, 2020-12, Vol.55 (6), p.868-876</ispartof><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd</rights><rights>2020 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.</rights><rights>2020 John Wiley & Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4199-cf3f542bf15002df9d9100c1340ae8cf64b5ae60b29efb4bb227444c8aaa6c0f3</citedby><cites>FETCH-LOGICAL-c4199-cf3f542bf15002df9d9100c1340ae8cf64b5ae60b29efb4bb227444c8aaa6c0f3</cites><orcidid>0000-0002-0045-9597 ; 0000-0002-7976-8594</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjre.12779$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjre.12779$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32583887$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Ae Ri</creatorcontrib><creatorcontrib>Kim, Ji‑Hye</creatorcontrib><creatorcontrib>Choi, Yun Hui</creatorcontrib><creatorcontrib>Jeon, Yeong‐Eui</creatorcontrib><creatorcontrib>Cha, Jeong‑Heon</creatorcontrib><creatorcontrib>Bak, Eun‑Jung</creatorcontrib><creatorcontrib>Yoo, Yun‑Jung</creatorcontrib><title>The presence of neutrophils causes RANKL expression in periodontal tissue, giving rise to osteoclast formation</title><title>Journal of periodontal research</title><addtitle>J Periodontal Res</addtitle><description>Backgrounds and Objective
Increased neutrophil infiltration and osteoclast formation are key characteristics of periodontitis. The effect of these neutrophils on osteoclast formation in periodontitis remains unclear. Therefore, we investigated the effects of neutrophils on osteoclast formation in a neutrophil‐deficient mouse model of periodontitis.
Methods
Anti‐Ly6G antibody (Ab) was used for neutrophil depletion in two mouse models: periodontitis and air pouch. In the periodontitis experiments, mice were divided into PBS‐administered control (C), control Ab‐administered periodontitis (P), and anti‐Ly6G Ab‐administered periodontitis (P + Ly6G) groups. Periodontitis was induced by ligature of mandibular first molars. In the air pouch experiments, mice were divided into PBS‐administered (C), LPS and control Ab‐administered (LPS), and LPS and anti‐Ly6G Ab‐administered (LPS + Ly6G) groups. Neutrophil migration into air pouches was induced by LPS injection. Flow cytometry was used to examine CD11b+Ly6G+ neutrophils in the blood of periodontitis mice and CD11b+Ly6G+RANKL+ neutrophils in exudates of air pouch mice. In periodontal tissue, Ly6G+ neutrophil and RANKL+ cell numbers in periodontal ligament and alveolar bone areas were estimated using immunohistochemistry, osteoclast numbers were measured using TRAP assay, and alveolar bone loss was determined by H&E staining.
Results
In blood, CD11b+Ly6G+ neutrophils were found in greater percentage in the P group than in the C group on days 3 and 7. However, the percentage of neutrophils was lower in the P + Ly6G group than in the C and P groups. In periodontal tissue, the numbers of Ly6G+ neutrophils and RANKL+ cells were lower in the P + Ly6G group than in the P group on day 3. Ly6G+ neutrophil numbers decreased more in the P + Ly6G group than in the P group on day 7, but RANKL+ cell numbers did not decrease in the P + Ly6G group. In exudates, the number of CD11b+Ly6G+RANKL+ neutrophils was greater in the LPS group than in the C and LPS + Ly6G groups. On days 3 and 7, the numbers of osteoclasts and alveolar bone loss were greater in periodontal tissue in the P and P + Ly6G groups than in the C group. Interestingly, there were fewer osteoclasts in the P + Ly6G group than in the P group on day 3.
Conclusion
Neutrophil deficiency caused a reduction in numbers of both RANKL+ cells and osteoclasts in periodontitis‐induced tissues only on day 3. Furthermore, in the LPS‐injected air pouch model, neutrophil deficiency reduced the influx of RANKL+ neutrophils. These findings suggest that the presence of neutrophils induces RANKL expression and could induce osteoclast formation in the early stages of periodontitis.</description><subject>Alveolar bone</subject><subject>Alveolar Bone Loss</subject><subject>Animal models</subject><subject>Animals</subject><subject>Bone loss</subject><subject>CD11b antigen</subject><subject>Exudates</subject><subject>Flow cytometry</subject><subject>Gum disease</subject><subject>Immunohistochemistry</subject><subject>Leukocyte migration</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lipopolysaccharides</subject><subject>Mice</subject><subject>Molars</subject><subject>Neutrophils</subject><subject>Neutrophils - physiology</subject><subject>Osteoclasts</subject><subject>Periodontal ligament</subject><subject>Periodontitis</subject><subject>Periodontium</subject><subject>RANK Ligand - metabolism</subject><subject>RANKL</subject><subject>Teeth</subject><subject>TRANCE protein</subject><issn>0022-3484</issn><issn>1600-0765</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10ctqGzEUBmBREhrH7SIvEATZNJCJJY3momUIuTQ1LQR3PWjkI1tmLE11Zprk7SPXaRaFaiMEn34O5yfkhLNLns5sE-GSi6pSH8iEl4xlrCqLAzJhTIgsl7U8IseIG5beZaU-kqNcFHVe19WE-MUaaB8BwRugwVIP4xBDv3YdUqNHBKSPV9-_zSk87xi64KnztIfowjL4QXd0cIgjXNCV--38ikaHQIdAAw4QTKdxoDbErR7S10_k0OoO4fPbPSU_b28W1_fZ_Mfd1-ureWYkVyozNreFFK3lRZp5adVSccYMzyXTUBtbyrbQULJWKLCtbFshKimlqbXWpWE2n5Iv-9w-hl8j4NBsHRroOu0hjNgIySvJCi5Eomf_0E0Yo0_TJVUoVdUlq5M63ysTA2IE2_TRbXV8aThrdiU0qYTmTwnJnr4lju0Wlu_y79YTmO3Bk-vg5f9JzcPjzT7yFQBFkgc</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Kim, Ae Ri</creator><creator>Kim, Ji‑Hye</creator><creator>Choi, Yun Hui</creator><creator>Jeon, Yeong‐Eui</creator><creator>Cha, Jeong‑Heon</creator><creator>Bak, Eun‑Jung</creator><creator>Yoo, Yun‑Jung</creator><general>Wiley Subscription Services, 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>7QP</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0045-9597</orcidid><orcidid>https://orcid.org/0000-0002-7976-8594</orcidid></search><sort><creationdate>202012</creationdate><title>The presence of neutrophils causes RANKL expression in periodontal tissue, giving rise to osteoclast formation</title><author>Kim, Ae Ri ; Kim, Ji‑Hye ; Choi, Yun Hui ; Jeon, Yeong‐Eui ; Cha, Jeong‑Heon ; Bak, Eun‑Jung ; Yoo, Yun‑Jung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4199-cf3f542bf15002df9d9100c1340ae8cf64b5ae60b29efb4bb227444c8aaa6c0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alveolar bone</topic><topic>Alveolar Bone Loss</topic><topic>Animal models</topic><topic>Animals</topic><topic>Bone loss</topic><topic>CD11b antigen</topic><topic>Exudates</topic><topic>Flow cytometry</topic><topic>Gum disease</topic><topic>Immunohistochemistry</topic><topic>Leukocyte migration</topic><topic>Leukocytes (neutrophilic)</topic><topic>Lipopolysaccharides</topic><topic>Mice</topic><topic>Molars</topic><topic>Neutrophils</topic><topic>Neutrophils - physiology</topic><topic>Osteoclasts</topic><topic>Periodontal ligament</topic><topic>Periodontitis</topic><topic>Periodontium</topic><topic>RANK Ligand - metabolism</topic><topic>RANKL</topic><topic>Teeth</topic><topic>TRANCE protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Ae Ri</creatorcontrib><creatorcontrib>Kim, Ji‑Hye</creatorcontrib><creatorcontrib>Choi, Yun Hui</creatorcontrib><creatorcontrib>Jeon, Yeong‐Eui</creatorcontrib><creatorcontrib>Cha, Jeong‑Heon</creatorcontrib><creatorcontrib>Bak, Eun‑Jung</creatorcontrib><creatorcontrib>Yoo, Yun‑Jung</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of periodontal research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ae Ri</au><au>Kim, Ji‑Hye</au><au>Choi, Yun Hui</au><au>Jeon, Yeong‐Eui</au><au>Cha, Jeong‑Heon</au><au>Bak, Eun‑Jung</au><au>Yoo, Yun‑Jung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The presence of neutrophils causes RANKL expression in periodontal tissue, giving rise to osteoclast formation</atitle><jtitle>Journal of periodontal research</jtitle><addtitle>J Periodontal Res</addtitle><date>2020-12</date><risdate>2020</risdate><volume>55</volume><issue>6</issue><spage>868</spage><epage>876</epage><pages>868-876</pages><issn>0022-3484</issn><eissn>1600-0765</eissn><abstract>Backgrounds and Objective
Increased neutrophil infiltration and osteoclast formation are key characteristics of periodontitis. The effect of these neutrophils on osteoclast formation in periodontitis remains unclear. Therefore, we investigated the effects of neutrophils on osteoclast formation in a neutrophil‐deficient mouse model of periodontitis.
Methods
Anti‐Ly6G antibody (Ab) was used for neutrophil depletion in two mouse models: periodontitis and air pouch. In the periodontitis experiments, mice were divided into PBS‐administered control (C), control Ab‐administered periodontitis (P), and anti‐Ly6G Ab‐administered periodontitis (P + Ly6G) groups. Periodontitis was induced by ligature of mandibular first molars. In the air pouch experiments, mice were divided into PBS‐administered (C), LPS and control Ab‐administered (LPS), and LPS and anti‐Ly6G Ab‐administered (LPS + Ly6G) groups. Neutrophil migration into air pouches was induced by LPS injection. Flow cytometry was used to examine CD11b+Ly6G+ neutrophils in the blood of periodontitis mice and CD11b+Ly6G+RANKL+ neutrophils in exudates of air pouch mice. In periodontal tissue, Ly6G+ neutrophil and RANKL+ cell numbers in periodontal ligament and alveolar bone areas were estimated using immunohistochemistry, osteoclast numbers were measured using TRAP assay, and alveolar bone loss was determined by H&E staining.
Results
In blood, CD11b+Ly6G+ neutrophils were found in greater percentage in the P group than in the C group on days 3 and 7. However, the percentage of neutrophils was lower in the P + Ly6G group than in the C and P groups. In periodontal tissue, the numbers of Ly6G+ neutrophils and RANKL+ cells were lower in the P + Ly6G group than in the P group on day 3. Ly6G+ neutrophil numbers decreased more in the P + Ly6G group than in the P group on day 7, but RANKL+ cell numbers did not decrease in the P + Ly6G group. In exudates, the number of CD11b+Ly6G+RANKL+ neutrophils was greater in the LPS group than in the C and LPS + Ly6G groups. On days 3 and 7, the numbers of osteoclasts and alveolar bone loss were greater in periodontal tissue in the P and P + Ly6G groups than in the C group. Interestingly, there were fewer osteoclasts in the P + Ly6G group than in the P group on day 3.
Conclusion
Neutrophil deficiency caused a reduction in numbers of both RANKL+ cells and osteoclasts in periodontitis‐induced tissues only on day 3. Furthermore, in the LPS‐injected air pouch model, neutrophil deficiency reduced the influx of RANKL+ neutrophils. These findings suggest that the presence of neutrophils induces RANKL expression and could induce osteoclast formation in the early stages of periodontitis.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>32583887</pmid><doi>10.1111/jre.12779</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0045-9597</orcidid><orcidid>https://orcid.org/0000-0002-7976-8594</orcidid></addata></record> |
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subjects | Alveolar bone Alveolar Bone Loss Animal models Animals Bone loss CD11b antigen Exudates Flow cytometry Gum disease Immunohistochemistry Leukocyte migration Leukocytes (neutrophilic) Lipopolysaccharides Mice Molars Neutrophils Neutrophils - physiology Osteoclasts Periodontal ligament Periodontitis Periodontium RANK Ligand - metabolism RANKL Teeth TRANCE protein |
title | The presence of neutrophils causes RANKL expression in periodontal tissue, giving rise to osteoclast formation |
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