Profiling of the three circulating monocyte subpopulations in human obesity
Three subpopulations of circulating monocytes have been described: CD14(2+)CD16(-) (classical monocytes [CM]), CD14(2+)CD16(+) (intermediate monocytes [IM]), and CD14(+)CD16(2+) (nonclassical monocytes [NCM]). We previously showed that obesity is associated with an increased proportion of IM and NCM...
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description | Three subpopulations of circulating monocytes have been described: CD14(2+)CD16(-) (classical monocytes [CM]), CD14(2+)CD16(+) (intermediate monocytes [IM]), and CD14(+)CD16(2+) (nonclassical monocytes [NCM]). We previously showed that obesity is associated with an increased proportion of IM and NCM. Our objective is to decipher the migratory and inflammatory functions of each monocyte subset in obesity-related low-grade inflammation. Twenty-six healthy, normal-weight and nondiabetic volunteers (C) and 40 obese nondiabetic (Ob) individuals were included in this study. We explored the gene expression profile of 18 inflammatory genes in each subset of C and Ob subjects and measured protein expression of the upregulated genes. We then tested their functional response to TLR signaling in both groups. We showed an increased expression of CX3CR1 in all monocyte subpopulations and of CCR2 and CCR5 in CM and IM in the Ob group. We found negative correlation between CCR2 and CX3CR1 expressions and high-density lipoprotein-cholesterol, whereas CCR5 expression was positively linked to obesity-related metabolic traits. Production of inflammatory proteins upon bacterial LPS and viral ssRNA stimulation was higher in CM and NCM of the Ob group compared with the C group. Our work highlights an enhanced inflammatory phenotype of monocytes with a higher response to TLR4 and TLR8 stimulations in obesity. Moreover, it suggests an increased migration capacity of CM and IM subpopulations. |
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We previously showed that obesity is associated with an increased proportion of IM and NCM. Our objective is to decipher the migratory and inflammatory functions of each monocyte subset in obesity-related low-grade inflammation. Twenty-six healthy, normal-weight and nondiabetic volunteers (C) and 40 obese nondiabetic (Ob) individuals were included in this study. We explored the gene expression profile of 18 inflammatory genes in each subset of C and Ob subjects and measured protein expression of the upregulated genes. We then tested their functional response to TLR signaling in both groups. We showed an increased expression of CX3CR1 in all monocyte subpopulations and of CCR2 and CCR5 in CM and IM in the Ob group. We found negative correlation between CCR2 and CX3CR1 expressions and high-density lipoprotein-cholesterol, whereas CCR5 expression was positively linked to obesity-related metabolic traits. Production of inflammatory proteins upon bacterial LPS and viral ssRNA stimulation was higher in CM and NCM of the Ob group compared with the C group. Our work highlights an enhanced inflammatory phenotype of monocytes with a higher response to TLR4 and TLR8 stimulations in obesity. Moreover, it suggests an increased migration capacity of CM and IM subpopulations.</description><identifier>ISSN: 0022-1767</identifier><identifier>EISSN: 1550-6606</identifier><identifier>DOI: 10.4049/jimmunol.1402655</identifier><identifier>PMID: 25786686</identifier><language>eng</language><publisher>United States: Publisher : Baltimore : Williams & Wilkins, c1950-. 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We previously showed that obesity is associated with an increased proportion of IM and NCM. Our objective is to decipher the migratory and inflammatory functions of each monocyte subset in obesity-related low-grade inflammation. Twenty-six healthy, normal-weight and nondiabetic volunteers (C) and 40 obese nondiabetic (Ob) individuals were included in this study. We explored the gene expression profile of 18 inflammatory genes in each subset of C and Ob subjects and measured protein expression of the upregulated genes. We then tested their functional response to TLR signaling in both groups. We showed an increased expression of CX3CR1 in all monocyte subpopulations and of CCR2 and CCR5 in CM and IM in the Ob group. We found negative correlation between CCR2 and CX3CR1 expressions and high-density lipoprotein-cholesterol, whereas CCR5 expression was positively linked to obesity-related metabolic traits. Production of inflammatory proteins upon bacterial LPS and viral ssRNA stimulation was higher in CM and NCM of the Ob group compared with the C group. Our work highlights an enhanced inflammatory phenotype of monocytes with a higher response to TLR4 and TLR8 stimulations in obesity. Moreover, it suggests an increased migration capacity of CM and IM subpopulations.</description><subject>Adult</subject><subject>CX3C Chemokine Receptor 1</subject><subject>Female</subject><subject>Gene Expression Profiling</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Gene Expression Regulation - immunology</subject><subject>GPI-Linked Proteins - immunology</subject><subject>Humans</subject><subject>Immunology</subject><subject>Inflammation Mediators - immunology</subject><subject>Innate immunity</subject><subject>Life Sciences</subject><subject>Lipopolysaccharide Receptors - immunology</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Male</subject><subject>Monocytes - immunology</subject><subject>Monocytes - pathology</subject><subject>Obesity</subject><subject>Receptors, CCR2 - immunology</subject><subject>Receptors, CCR5 - immunology</subject><subject>Receptors, Chemokine - immunology</subject><subject>Receptors, IgG - immunology</subject><subject>Toll-Like Receptor 4 - agonists</subject><subject>Toll-Like Receptor 4 - immunology</subject><subject>Toll-Like Receptor 8 - agonists</subject><subject>Toll-Like Receptor 8 - immunology</subject><issn>0022-1767</issn><issn>1550-6606</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkb1v2zAQxYmgQeK43TsVGptBzpEij9QYGElc1EAyJDNB8aNmIImuKAXwf187drJ2OBzw7vceDniEfKew4MDrm9fYdVOf2gXlwFCIMzKjQkCJCPiFzAAYK6lEeUmucn4FAATGL8glE1IhKpyR309DCrGN_Z8ihWLc-P0M3hc2DnZqzXg4dKlPdjf6Ik_NNm3f5dTnIvbFZupMX6TG5zjuvpLzYNrsv532nLzc3z0vV-X68eHX8nZdWg5qLF3Aug4c0VUUlbSMVc5VXrrGMg4GK6E8mkY1zpogZO0YY8hDsMEpXlWmmpPrY-7GtHo7xM4MO51M1KvbtT5owARnAPUb3bM_j-x2SH8nn0fdxWx925repylrqkAhrWsq_4-ipIwKkAcUjqgdUs6DD59vUNCHZvRHM_rUzN7y45Q-NZ13n4aPKqp_j_uLow</recordid><startdate>20150415</startdate><enddate>20150415</enddate><creator>Devêvre, Estelle F</creator><creator>Renovato-Martins, Mariana</creator><creator>Clément, Karine</creator><creator>Sautès-Fridman, Catherine</creator><creator>Cremer, Isabelle</creator><creator>Poitou, Christine</creator><general>Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists</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><scope>7T5</scope><scope>H94</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-1735-8722</orcidid><orcidid>https://orcid.org/0000-0002-0963-1031</orcidid><orcidid>https://orcid.org/0000-0002-8347-8987</orcidid><orcidid>https://orcid.org/0000-0003-4619-6785</orcidid><orcidid>https://orcid.org/0000-0002-2489-3355</orcidid><orcidid>https://orcid.org/0000-0001-7769-6331</orcidid></search><sort><creationdate>20150415</creationdate><title>Profiling of the three circulating monocyte subpopulations in human obesity</title><author>Devêvre, Estelle F ; Renovato-Martins, Mariana ; Clément, Karine ; Sautès-Fridman, Catherine ; Cremer, Isabelle ; Poitou, Christine</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-df699f466d31687c223dd3e7dbc240a6358e6ab8bdcaf579d22264ffcfd8433a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>CX3C Chemokine Receptor 1</topic><topic>Female</topic><topic>Gene Expression Profiling</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Gene Expression Regulation - immunology</topic><topic>GPI-Linked Proteins - immunology</topic><topic>Humans</topic><topic>Immunology</topic><topic>Inflammation Mediators - immunology</topic><topic>Innate immunity</topic><topic>Life Sciences</topic><topic>Lipopolysaccharide Receptors - immunology</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Male</topic><topic>Monocytes - immunology</topic><topic>Monocytes - pathology</topic><topic>Obesity</topic><topic>Receptors, CCR2 - immunology</topic><topic>Receptors, CCR5 - immunology</topic><topic>Receptors, Chemokine - immunology</topic><topic>Receptors, IgG - immunology</topic><topic>Toll-Like Receptor 4 - agonists</topic><topic>Toll-Like Receptor 4 - immunology</topic><topic>Toll-Like Receptor 8 - agonists</topic><topic>Toll-Like Receptor 8 - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Devêvre, Estelle F</creatorcontrib><creatorcontrib>Renovato-Martins, Mariana</creatorcontrib><creatorcontrib>Clément, Karine</creatorcontrib><creatorcontrib>Sautès-Fridman, Catherine</creatorcontrib><creatorcontrib>Cremer, Isabelle</creatorcontrib><creatorcontrib>Poitou, Christine</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>The Journal of immunology (1950)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Devêvre, Estelle F</au><au>Renovato-Martins, Mariana</au><au>Clément, Karine</au><au>Sautès-Fridman, Catherine</au><au>Cremer, Isabelle</au><au>Poitou, Christine</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Profiling of the three circulating monocyte subpopulations in human obesity</atitle><jtitle>The Journal of immunology (1950)</jtitle><addtitle>J Immunol</addtitle><date>2015-04-15</date><risdate>2015</risdate><volume>194</volume><issue>8</issue><spage>3917</spage><epage>3923</epage><pages>3917-3923</pages><issn>0022-1767</issn><eissn>1550-6606</eissn><abstract>Three subpopulations of circulating monocytes have been described: CD14(2+)CD16(-) (classical monocytes [CM]), CD14(2+)CD16(+) (intermediate monocytes [IM]), and CD14(+)CD16(2+) (nonclassical monocytes [NCM]). We previously showed that obesity is associated with an increased proportion of IM and NCM. Our objective is to decipher the migratory and inflammatory functions of each monocyte subset in obesity-related low-grade inflammation. Twenty-six healthy, normal-weight and nondiabetic volunteers (C) and 40 obese nondiabetic (Ob) individuals were included in this study. We explored the gene expression profile of 18 inflammatory genes in each subset of C and Ob subjects and measured protein expression of the upregulated genes. We then tested their functional response to TLR signaling in both groups. We showed an increased expression of CX3CR1 in all monocyte subpopulations and of CCR2 and CCR5 in CM and IM in the Ob group. We found negative correlation between CCR2 and CX3CR1 expressions and high-density lipoprotein-cholesterol, whereas CCR5 expression was positively linked to obesity-related metabolic traits. Production of inflammatory proteins upon bacterial LPS and viral ssRNA stimulation was higher in CM and NCM of the Ob group compared with the C group. Our work highlights an enhanced inflammatory phenotype of monocytes with a higher response to TLR4 and TLR8 stimulations in obesity. Moreover, it suggests an increased migration capacity of CM and IM subpopulations.</abstract><cop>United States</cop><pub>Publisher : Baltimore : Williams & Wilkins, c1950-. Latest Publisher : Bethesda, MD : American Association of Immunologists</pub><pmid>25786686</pmid><doi>10.4049/jimmunol.1402655</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-1735-8722</orcidid><orcidid>https://orcid.org/0000-0002-0963-1031</orcidid><orcidid>https://orcid.org/0000-0002-8347-8987</orcidid><orcidid>https://orcid.org/0000-0003-4619-6785</orcidid><orcidid>https://orcid.org/0000-0002-2489-3355</orcidid><orcidid>https://orcid.org/0000-0001-7769-6331</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult CX3C Chemokine Receptor 1 Female Gene Expression Profiling Gene Expression Regulation - drug effects Gene Expression Regulation - immunology GPI-Linked Proteins - immunology Humans Immunology Inflammation Mediators - immunology Innate immunity Life Sciences Lipopolysaccharide Receptors - immunology Lipopolysaccharides - pharmacology Male Monocytes - immunology Monocytes - pathology Obesity Receptors, CCR2 - immunology Receptors, CCR5 - immunology Receptors, Chemokine - immunology Receptors, IgG - immunology Toll-Like Receptor 4 - agonists Toll-Like Receptor 4 - immunology Toll-Like Receptor 8 - agonists Toll-Like Receptor 8 - immunology |
title | Profiling of the three circulating monocyte subpopulations in human obesity |
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