Induction of M2 Macrophages Prevents Bone Loss in Murine Periodontitis Models
Periodontitis is characterized by the progressive destruction of tooth-supporting alveolar bone, which is mainly caused by chronic inflammation in response to persistent bacterial insult. It has recently become clear that the pathogenesis of periodontitis is associated with a high ratio of proinflam...
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creator | Zhuang, Z. Yoshizawa-Smith, S. Glowacki, A. Maltos, K. Pacheco, C. Shehabeldin, M. Mulkeen, M. Myers, N. Chong, R. Verdelis, K. Garlet, G.P. Little, S. Sfeir, C. |
description | Periodontitis is characterized by the progressive destruction of tooth-supporting alveolar bone, which is mainly caused by chronic inflammation in response to persistent bacterial insult. It has recently become clear that the pathogenesis of periodontitis is associated with a high ratio of proinflammatory M1 (classically activated) macrophages to anti-inflammatory M2 (alternatively activated). To decrease the inflammatory activity, we locally delivered the C-C motif chemokine ligand 2 (CCL2) using controlled-release microparticles (MPs). CCL2 is known to promote chemotaxis of M0 or M2 phenotype macrophages to the inflamed site and induce M2 phenotype polarization locally. Our in vitro data showed that CCL2 increased the number of M2 phenotype macrophages, decreased TNF-α secretion, and enhanced chemotaxis of RAW264.7 cells toward CCL2 MPs. Moreover, we induced periodontal disease in 2 animal models through inoculation of Porphyromonas gingivalis and ligature around the murine molar. Micro–computed tomography analysis showed significant reduction of alveolar bone loss in the CCL2 MP treatment group when compared with a blank MP group and a no-treatment periodontitis group in both models. Immunohistologic analysis showed a significant increase in the M2 phenotype subset and a decrease in the M1 phenotype subset in the CCL2 MP group of the P. gingivalis–induced model. Also, in both models, tartrate-resistant acidic phosphatase staining showed significantly fewer numbers of osteoclasts in the CCL2 MP group in alveolar bone area. Moreover, quantitative polymerase chain reaction results showed a significant increase in IL-1RA (interleukin 1 receptor antagonist) mRNA expression and a decrease in RANKL (receptor activator of nuclear factor kappa-Β ligand) mRNA expression in the CCL2 MP group in the ligature model. In summary, manipulation of endogenous M2 phenotype macrophages with CCL2 MPs decreased the M1 phenotype:M2 phenotype ratio and prevented alveolar bone loss in mouse periodontitis models. The delivery of CCL2 MPs provides a novel approach to treat periodontal disease. |
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It has recently become clear that the pathogenesis of periodontitis is associated with a high ratio of proinflammatory M1 (classically activated) macrophages to anti-inflammatory M2 (alternatively activated). To decrease the inflammatory activity, we locally delivered the C-C motif chemokine ligand 2 (CCL2) using controlled-release microparticles (MPs). CCL2 is known to promote chemotaxis of M0 or M2 phenotype macrophages to the inflamed site and induce M2 phenotype polarization locally. Our in vitro data showed that CCL2 increased the number of M2 phenotype macrophages, decreased TNF-α secretion, and enhanced chemotaxis of RAW264.7 cells toward CCL2 MPs. Moreover, we induced periodontal disease in 2 animal models through inoculation of Porphyromonas gingivalis and ligature around the murine molar. Micro–computed tomography analysis showed significant reduction of alveolar bone loss in the CCL2 MP treatment group when compared with a blank MP group and a no-treatment periodontitis group in both models. Immunohistologic analysis showed a significant increase in the M2 phenotype subset and a decrease in the M1 phenotype subset in the CCL2 MP group of the P. gingivalis–induced model. Also, in both models, tartrate-resistant acidic phosphatase staining showed significantly fewer numbers of osteoclasts in the CCL2 MP group in alveolar bone area. Moreover, quantitative polymerase chain reaction results showed a significant increase in IL-1RA (interleukin 1 receptor antagonist) mRNA expression and a decrease in RANKL (receptor activator of nuclear factor kappa-Β ligand) mRNA expression in the CCL2 MP group in the ligature model. In summary, manipulation of endogenous M2 phenotype macrophages with CCL2 MPs decreased the M1 phenotype:M2 phenotype ratio and prevented alveolar bone loss in mouse periodontitis models. The delivery of CCL2 MPs provides a novel approach to treat periodontal disease.</description><identifier>ISSN: 0022-0345</identifier><identifier>EISSN: 1544-0591</identifier><identifier>DOI: 10.1177/0022034518805984</identifier><identifier>PMID: 30392438</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Alveolar bone ; Alveolar Bone Loss - prevention & control ; Animal models ; Animals ; Bone loss ; Bone marrow ; Cell adhesion & migration ; Chemokines ; Chemotaxis ; Computed tomography ; Controlled release ; Cytokines ; Data analysis ; Dentistry ; Disease ; Disease Models, Animal ; Female ; Gene expression ; Genotype & phenotype ; Gum disease ; Inflammation ; Inoculation ; Interleukin 1 ; Interleukin 1 receptor antagonist ; Interleukin 1 receptors ; Ligands ; Macrophages ; Macrophages - physiology ; Mice ; Microparticles ; Monocyte chemoattractant protein 1 ; Osteoclasts ; Penicillin ; Periodontal diseases ; Periodontitis ; Periodontitis - physiopathology ; Phenotypes ; Polymerase chain reaction ; Porphyromonas gingivalis ; Research Reports ; TRANCE protein ; Tumor necrosis factor-α ; X-Ray Microtomography</subject><ispartof>Journal of dental research, 2019-02, Vol.98 (2), p.200-208</ispartof><rights>International & American Associations for Dental Research 2018</rights><rights>International & American Associations for Dental Research 2018 2018 International & American Associations for Dental Research</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-7c85a812e8437eae04a65155860482625165cbee45e072a6f94ac24456e533283</citedby><cites>FETCH-LOGICAL-c528t-7c85a812e8437eae04a65155860482625165cbee45e072a6f94ac24456e533283</cites><orcidid>0000-0002-5071-8382</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/0022034518805984$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/0022034518805984$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>230,314,776,780,881,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30392438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhuang, Z.</creatorcontrib><creatorcontrib>Yoshizawa-Smith, S.</creatorcontrib><creatorcontrib>Glowacki, A.</creatorcontrib><creatorcontrib>Maltos, K.</creatorcontrib><creatorcontrib>Pacheco, C.</creatorcontrib><creatorcontrib>Shehabeldin, M.</creatorcontrib><creatorcontrib>Mulkeen, M.</creatorcontrib><creatorcontrib>Myers, N.</creatorcontrib><creatorcontrib>Chong, R.</creatorcontrib><creatorcontrib>Verdelis, K.</creatorcontrib><creatorcontrib>Garlet, G.P.</creatorcontrib><creatorcontrib>Little, S.</creatorcontrib><creatorcontrib>Sfeir, C.</creatorcontrib><title>Induction of M2 Macrophages Prevents Bone Loss in Murine Periodontitis Models</title><title>Journal of dental research</title><addtitle>J Dent Res</addtitle><description>Periodontitis is characterized by the progressive destruction of tooth-supporting alveolar bone, which is mainly caused by chronic inflammation in response to persistent bacterial insult. It has recently become clear that the pathogenesis of periodontitis is associated with a high ratio of proinflammatory M1 (classically activated) macrophages to anti-inflammatory M2 (alternatively activated). To decrease the inflammatory activity, we locally delivered the C-C motif chemokine ligand 2 (CCL2) using controlled-release microparticles (MPs). CCL2 is known to promote chemotaxis of M0 or M2 phenotype macrophages to the inflamed site and induce M2 phenotype polarization locally. Our in vitro data showed that CCL2 increased the number of M2 phenotype macrophages, decreased TNF-α secretion, and enhanced chemotaxis of RAW264.7 cells toward CCL2 MPs. Moreover, we induced periodontal disease in 2 animal models through inoculation of Porphyromonas gingivalis and ligature around the murine molar. Micro–computed tomography analysis showed significant reduction of alveolar bone loss in the CCL2 MP treatment group when compared with a blank MP group and a no-treatment periodontitis group in both models. Immunohistologic analysis showed a significant increase in the M2 phenotype subset and a decrease in the M1 phenotype subset in the CCL2 MP group of the P. gingivalis–induced model. Also, in both models, tartrate-resistant acidic phosphatase staining showed significantly fewer numbers of osteoclasts in the CCL2 MP group in alveolar bone area. Moreover, quantitative polymerase chain reaction results showed a significant increase in IL-1RA (interleukin 1 receptor antagonist) mRNA expression and a decrease in RANKL (receptor activator of nuclear factor kappa-Β ligand) mRNA expression in the CCL2 MP group in the ligature model. In summary, manipulation of endogenous M2 phenotype macrophages with CCL2 MPs decreased the M1 phenotype:M2 phenotype ratio and prevented alveolar bone loss in mouse periodontitis models. The delivery of CCL2 MPs provides a novel approach to treat periodontal disease.</description><subject>Alveolar bone</subject><subject>Alveolar Bone Loss - prevention & control</subject><subject>Animal models</subject><subject>Animals</subject><subject>Bone loss</subject><subject>Bone marrow</subject><subject>Cell adhesion & migration</subject><subject>Chemokines</subject><subject>Chemotaxis</subject><subject>Computed tomography</subject><subject>Controlled release</subject><subject>Cytokines</subject><subject>Data analysis</subject><subject>Dentistry</subject><subject>Disease</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Gene expression</subject><subject>Genotype & phenotype</subject><subject>Gum disease</subject><subject>Inflammation</subject><subject>Inoculation</subject><subject>Interleukin 1</subject><subject>Interleukin 1 receptor antagonist</subject><subject>Interleukin 1 receptors</subject><subject>Ligands</subject><subject>Macrophages</subject><subject>Macrophages - physiology</subject><subject>Mice</subject><subject>Microparticles</subject><subject>Monocyte chemoattractant protein 1</subject><subject>Osteoclasts</subject><subject>Penicillin</subject><subject>Periodontal diseases</subject><subject>Periodontitis</subject><subject>Periodontitis - physiopathology</subject><subject>Phenotypes</subject><subject>Polymerase chain reaction</subject><subject>Porphyromonas gingivalis</subject><subject>Research Reports</subject><subject>TRANCE protein</subject><subject>Tumor necrosis factor-α</subject><subject>X-Ray Microtomography</subject><issn>0022-0345</issn><issn>1544-0591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUlLBDEQhYMoOi53TxLw4qU1ezIXQcUNptGDnkPsqdFITzIm3YL_3jTjDp5CUV-9qpeH0C4lh5RqfUQIY4QLSY0hcmzEChpRKURVCrqKRkO7GvobaDPnZ0LomBm-jjY44WMmuBmh-jpM-6bzMeA4wzXDtWtSXDy5R8j4NsErhC7j0xgAT2LO2Adc98mX8haSj9MYOt_5jOs4hTZvo7WZazPsfLxb6P7i_O7sqprcXF6fnUyqRjLTVbox0hnKwAiuwQERTkkqpVFEGKaYpEo2DwBCAtHMqdlYuIYJIRVIzouFLXS81F30D3OYNuXI5Fq7SH7u0puNztvfneCf7GN8tUorqrkqAgcfAim-9JA7O_e5gbZ1AWKfLaOcECm0GHbt_0GfY59CsWdZgRTlWg4UWVLl93JOMPs6hhI7ZGX_ZlVG9n6a-Br4DKcA1RLIJY3vrf8KvgPr05nN</recordid><startdate>20190201</startdate><enddate>20190201</enddate><creator>Zhuang, Z.</creator><creator>Yoshizawa-Smith, S.</creator><creator>Glowacki, A.</creator><creator>Maltos, K.</creator><creator>Pacheco, C.</creator><creator>Shehabeldin, M.</creator><creator>Mulkeen, M.</creator><creator>Myers, N.</creator><creator>Chong, R.</creator><creator>Verdelis, K.</creator><creator>Garlet, G.P.</creator><creator>Little, S.</creator><creator>Sfeir, C.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, 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>K9.</scope><scope>NAPCQ</scope><scope>U9A</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5071-8382</orcidid></search><sort><creationdate>20190201</creationdate><title>Induction of M2 Macrophages Prevents Bone Loss in Murine Periodontitis Models</title><author>Zhuang, Z. ; Yoshizawa-Smith, S. ; Glowacki, A. ; Maltos, K. ; Pacheco, C. ; Shehabeldin, M. ; Mulkeen, M. ; Myers, N. ; Chong, R. ; Verdelis, K. ; Garlet, G.P. ; Little, S. ; Sfeir, C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-7c85a812e8437eae04a65155860482625165cbee45e072a6f94ac24456e533283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Alveolar bone</topic><topic>Alveolar Bone Loss - prevention & control</topic><topic>Animal models</topic><topic>Animals</topic><topic>Bone loss</topic><topic>Bone marrow</topic><topic>Cell adhesion & migration</topic><topic>Chemokines</topic><topic>Chemotaxis</topic><topic>Computed tomography</topic><topic>Controlled release</topic><topic>Cytokines</topic><topic>Data analysis</topic><topic>Dentistry</topic><topic>Disease</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Gene expression</topic><topic>Genotype & phenotype</topic><topic>Gum disease</topic><topic>Inflammation</topic><topic>Inoculation</topic><topic>Interleukin 1</topic><topic>Interleukin 1 receptor antagonist</topic><topic>Interleukin 1 receptors</topic><topic>Ligands</topic><topic>Macrophages</topic><topic>Macrophages - physiology</topic><topic>Mice</topic><topic>Microparticles</topic><topic>Monocyte chemoattractant protein 1</topic><topic>Osteoclasts</topic><topic>Penicillin</topic><topic>Periodontal diseases</topic><topic>Periodontitis</topic><topic>Periodontitis - physiopathology</topic><topic>Phenotypes</topic><topic>Polymerase chain reaction</topic><topic>Porphyromonas gingivalis</topic><topic>Research Reports</topic><topic>TRANCE protein</topic><topic>Tumor necrosis factor-α</topic><topic>X-Ray Microtomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhuang, Z.</creatorcontrib><creatorcontrib>Yoshizawa-Smith, S.</creatorcontrib><creatorcontrib>Glowacki, A.</creatorcontrib><creatorcontrib>Maltos, K.</creatorcontrib><creatorcontrib>Pacheco, C.</creatorcontrib><creatorcontrib>Shehabeldin, M.</creatorcontrib><creatorcontrib>Mulkeen, M.</creatorcontrib><creatorcontrib>Myers, N.</creatorcontrib><creatorcontrib>Chong, R.</creatorcontrib><creatorcontrib>Verdelis, K.</creatorcontrib><creatorcontrib>Garlet, G.P.</creatorcontrib><creatorcontrib>Little, S.</creatorcontrib><creatorcontrib>Sfeir, C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of dental research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhuang, Z.</au><au>Yoshizawa-Smith, S.</au><au>Glowacki, A.</au><au>Maltos, K.</au><au>Pacheco, C.</au><au>Shehabeldin, M.</au><au>Mulkeen, M.</au><au>Myers, N.</au><au>Chong, R.</au><au>Verdelis, K.</au><au>Garlet, G.P.</au><au>Little, S.</au><au>Sfeir, C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Induction of M2 Macrophages Prevents Bone Loss in Murine Periodontitis Models</atitle><jtitle>Journal of dental research</jtitle><addtitle>J Dent Res</addtitle><date>2019-02-01</date><risdate>2019</risdate><volume>98</volume><issue>2</issue><spage>200</spage><epage>208</epage><pages>200-208</pages><issn>0022-0345</issn><eissn>1544-0591</eissn><abstract>Periodontitis is characterized by the progressive destruction of tooth-supporting alveolar bone, which is mainly caused by chronic inflammation in response to persistent bacterial insult. It has recently become clear that the pathogenesis of periodontitis is associated with a high ratio of proinflammatory M1 (classically activated) macrophages to anti-inflammatory M2 (alternatively activated). To decrease the inflammatory activity, we locally delivered the C-C motif chemokine ligand 2 (CCL2) using controlled-release microparticles (MPs). CCL2 is known to promote chemotaxis of M0 or M2 phenotype macrophages to the inflamed site and induce M2 phenotype polarization locally. Our in vitro data showed that CCL2 increased the number of M2 phenotype macrophages, decreased TNF-α secretion, and enhanced chemotaxis of RAW264.7 cells toward CCL2 MPs. Moreover, we induced periodontal disease in 2 animal models through inoculation of Porphyromonas gingivalis and ligature around the murine molar. Micro–computed tomography analysis showed significant reduction of alveolar bone loss in the CCL2 MP treatment group when compared with a blank MP group and a no-treatment periodontitis group in both models. Immunohistologic analysis showed a significant increase in the M2 phenotype subset and a decrease in the M1 phenotype subset in the CCL2 MP group of the P. gingivalis–induced model. Also, in both models, tartrate-resistant acidic phosphatase staining showed significantly fewer numbers of osteoclasts in the CCL2 MP group in alveolar bone area. Moreover, quantitative polymerase chain reaction results showed a significant increase in IL-1RA (interleukin 1 receptor antagonist) mRNA expression and a decrease in RANKL (receptor activator of nuclear factor kappa-Β ligand) mRNA expression in the CCL2 MP group in the ligature model. In summary, manipulation of endogenous M2 phenotype macrophages with CCL2 MPs decreased the M1 phenotype:M2 phenotype ratio and prevented alveolar bone loss in mouse periodontitis models. The delivery of CCL2 MPs provides a novel approach to treat periodontal disease.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>30392438</pmid><doi>10.1177/0022034518805984</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-5071-8382</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alveolar bone Alveolar Bone Loss - prevention & control Animal models Animals Bone loss Bone marrow Cell adhesion & migration Chemokines Chemotaxis Computed tomography Controlled release Cytokines Data analysis Dentistry Disease Disease Models, Animal Female Gene expression Genotype & phenotype Gum disease Inflammation Inoculation Interleukin 1 Interleukin 1 receptor antagonist Interleukin 1 receptors Ligands Macrophages Macrophages - physiology Mice Microparticles Monocyte chemoattractant protein 1 Osteoclasts Penicillin Periodontal diseases Periodontitis Periodontitis - physiopathology Phenotypes Polymerase chain reaction Porphyromonas gingivalis Research Reports TRANCE protein Tumor necrosis factor-α X-Ray Microtomography |
title | Induction of M2 Macrophages Prevents Bone Loss in Murine Periodontitis Models |
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