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Phenotypic Changes in Macrophage Activation in a Model of Nonalcoholic Fatty Liver Disease using Microminipigs
Aim: Non-alcoholic fatty liver disease (NAFLD) is one of the most common chronic liver disorders associated with metabolic syndrome, and its prevalence has been on the rise. The pathogenesis of NAFLD has not yet been sufficiently elucidated due to the multifactorial nature of the disease, although t...
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Published in: | Journal of Atherosclerosis and Thrombosis 2021/08/01, Vol.28(8), pp.844-851 |
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creator | Yoshii, Daiki Nakagawa, Takenobu Komohara, Yoshihiro Kawaguchi, Hiroaki Yamada, Sohsuke Tanimoto, Akihide |
description | Aim: Non-alcoholic fatty liver disease (NAFLD) is one of the most common chronic liver disorders associated with metabolic syndrome, and its prevalence has been on the rise. The pathogenesis of NAFLD has not yet been sufficiently elucidated due to the multifactorial nature of the disease, although the activation of macrophages/Kupffer cells is considered to be involved. We previously reported an animal model of NAFLD using MicrominipigsTM (µMPs) fed high-fat diets containing cholesterol with or without cholic acid. The aim of this study was to investigate the phenotypic changes of macrophages that occur during the development of NAFLD. Methods: Immunohistochemistry of macrophages, lymphocytes, and stellate cells was performed using liver samples, and the density of positive cells was analyzed. Results: The number of Iba-1-positive macrophages increased with increasing cholesterol content in the diet. The numbers of CD163-positive macrophages and CD204-positive macrophages also increased with increasing cholesterol content in the diet; however, the proportion of CD204-positive macrophages among Iba-1-positive macrophages was significantly reduced by cholic acid supplementation. Conclusion: The results suggest that lipid accumulation induced macrophage recruitment in swine livers, and that the number of M2-like macrophages increased at the early stage of NAFLD, while the number of M1-like macrophages increased at the late stage of NAFLD, resulting in a liver condition like non-alcoholic steatohepatitis. We provide evidence of the phenotypic changes that occur in macrophages during the development of NAFLD that has never been reported before using µMPs. |
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The pathogenesis of NAFLD has not yet been sufficiently elucidated due to the multifactorial nature of the disease, although the activation of macrophages/Kupffer cells is considered to be involved. We previously reported an animal model of NAFLD using MicrominipigsTM (µMPs) fed high-fat diets containing cholesterol with or without cholic acid. The aim of this study was to investigate the phenotypic changes of macrophages that occur during the development of NAFLD. Methods: Immunohistochemistry of macrophages, lymphocytes, and stellate cells was performed using liver samples, and the density of positive cells was analyzed. Results: The number of Iba-1-positive macrophages increased with increasing cholesterol content in the diet. The numbers of CD163-positive macrophages and CD204-positive macrophages also increased with increasing cholesterol content in the diet; however, the proportion of CD204-positive macrophages among Iba-1-positive macrophages was significantly reduced by cholic acid supplementation. Conclusion: The results suggest that lipid accumulation induced macrophage recruitment in swine livers, and that the number of M2-like macrophages increased at the early stage of NAFLD, while the number of M1-like macrophages increased at the late stage of NAFLD, resulting in a liver condition like non-alcoholic steatohepatitis. We provide evidence of the phenotypic changes that occur in macrophages during the development of NAFLD that has never been reported before using µMPs.</description><identifier>ISSN: 1340-3478</identifier><identifier>EISSN: 1880-3873</identifier><identifier>DOI: 10.5551/jat.57703</identifier><identifier>PMID: 33012740</identifier><language>eng</language><publisher>Japan: Japan Atherosclerosis Society</publisher><subject>Animals ; Antigens, CD - metabolism ; Antigens, Differentiation, Myelomonocytic - metabolism ; Cholesterol - administration & dosage ; Cholesterol - toxicity ; Cholic Acid - administration & dosage ; Cholic Acid - toxicity ; Diet, High-Fat ; Disease Models, Animal ; Disease Progression ; Fatty liver disease ; Hepatic Stellate Cells - immunology ; Hepatic Stellate Cells - metabolism ; Hepatic Stellate Cells - pathology ; Lymphocytes - immunology ; Lymphocytes - metabolism ; Lymphocytes - pathology ; Macrophage ; Macrophage Activation - immunology ; Macrophages - immunology ; Macrophages - metabolism ; Macrophages - pathology ; Microminipig ; NAFLD ; NASH ; Non-alcoholic Fatty Liver Disease - chemically induced ; Non-alcoholic Fatty Liver Disease - immunology ; Non-alcoholic Fatty Liver Disease - pathology ; Original ; Phenotype ; Receptors, Cell Surface - metabolism ; Swine ; Swine, Miniature</subject><ispartof>Journal of Atherosclerosis and Thrombosis, 2021/08/01, Vol.28(8), pp.844-851</ispartof><rights>This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.</rights><rights>2021 Japan Atherosclerosis Society 2021</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c686t-f8d414c0efdf160bae64dda1ad169b4940f6c3ff549010d123ed1e23f690e1353</citedby><cites>FETCH-LOGICAL-c686t-f8d414c0efdf160bae64dda1ad169b4940f6c3ff549010d123ed1e23f690e1353</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326174/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8326174/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33012740$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yoshii, Daiki</creatorcontrib><creatorcontrib>Nakagawa, Takenobu</creatorcontrib><creatorcontrib>Komohara, Yoshihiro</creatorcontrib><creatorcontrib>Kawaguchi, Hiroaki</creatorcontrib><creatorcontrib>Yamada, Sohsuke</creatorcontrib><creatorcontrib>Tanimoto, Akihide</creatorcontrib><creatorcontrib>Department of Pathology</creatorcontrib><creatorcontrib>Department of Pathology and Laboratory Medicine</creatorcontrib><creatorcontrib>Kumamoto University</creatorcontrib><creatorcontrib>Kanazawa Medical University</creatorcontrib><creatorcontrib>Center for Metabolic Regulation of Healthy Aging</creatorcontrib><creatorcontrib>Department of Cell Pathology</creatorcontrib><creatorcontrib>Department of Hygiene and Health Promotion Medicine</creatorcontrib><creatorcontrib>Kagoshima University Graduate School of Medical and Dental Sciences</creatorcontrib><creatorcontrib>Graduate School of Medical Sciences</creatorcontrib><title>Phenotypic Changes in Macrophage Activation in a Model of Nonalcoholic Fatty Liver Disease using Microminipigs</title><title>Journal of Atherosclerosis and Thrombosis</title><addtitle>JAT</addtitle><description>Aim: Non-alcoholic fatty liver disease (NAFLD) is one of the most common chronic liver disorders associated with metabolic syndrome, and its prevalence has been on the rise. The pathogenesis of NAFLD has not yet been sufficiently elucidated due to the multifactorial nature of the disease, although the activation of macrophages/Kupffer cells is considered to be involved. We previously reported an animal model of NAFLD using MicrominipigsTM (µMPs) fed high-fat diets containing cholesterol with or without cholic acid. The aim of this study was to investigate the phenotypic changes of macrophages that occur during the development of NAFLD. Methods: Immunohistochemistry of macrophages, lymphocytes, and stellate cells was performed using liver samples, and the density of positive cells was analyzed. Results: The number of Iba-1-positive macrophages increased with increasing cholesterol content in the diet. The numbers of CD163-positive macrophages and CD204-positive macrophages also increased with increasing cholesterol content in the diet; however, the proportion of CD204-positive macrophages among Iba-1-positive macrophages was significantly reduced by cholic acid supplementation. Conclusion: The results suggest that lipid accumulation induced macrophage recruitment in swine livers, and that the number of M2-like macrophages increased at the early stage of NAFLD, while the number of M1-like macrophages increased at the late stage of NAFLD, resulting in a liver condition like non-alcoholic steatohepatitis. We provide evidence of the phenotypic changes that occur in macrophages during the development of NAFLD that has never been reported before using µMPs.</description><subject>Animals</subject><subject>Antigens, CD - metabolism</subject><subject>Antigens, Differentiation, Myelomonocytic - metabolism</subject><subject>Cholesterol - administration & dosage</subject><subject>Cholesterol - toxicity</subject><subject>Cholic Acid - administration & dosage</subject><subject>Cholic Acid - toxicity</subject><subject>Diet, High-Fat</subject><subject>Disease Models, Animal</subject><subject>Disease Progression</subject><subject>Fatty liver disease</subject><subject>Hepatic Stellate Cells - immunology</subject><subject>Hepatic Stellate Cells - metabolism</subject><subject>Hepatic Stellate Cells - pathology</subject><subject>Lymphocytes - immunology</subject><subject>Lymphocytes - metabolism</subject><subject>Lymphocytes - pathology</subject><subject>Macrophage</subject><subject>Macrophage Activation - immunology</subject><subject>Macrophages - immunology</subject><subject>Macrophages - metabolism</subject><subject>Macrophages - pathology</subject><subject>Microminipig</subject><subject>NAFLD</subject><subject>NASH</subject><subject>Non-alcoholic Fatty Liver Disease - chemically induced</subject><subject>Non-alcoholic Fatty Liver Disease - immunology</subject><subject>Non-alcoholic Fatty Liver Disease - pathology</subject><subject>Original</subject><subject>Phenotype</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Swine</subject><subject>Swine, Miniature</subject><issn>1340-3478</issn><issn>1880-3873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpVUU2P0zAQjRCIXRYO_AHkI3vo4q8kzgW0KrsLUgsc4GxNnUniKrFD7FT036_bLhUcPDPSe37z7Jdlbxm9yfOcfdhCvMnLkopn2SVTii6EKsXzNAuZZlmqi-xVCFtKhchz_jK7EIIyXkp6mbkfHTof96M1ZNmBazEQ68gazOTHDloktybaHUTr3QEAsvY19sQ35Jt30Bvf-T7dvYcY92RldziRzzYgBCRzsK4la5ukBuvsaNvwOnvRQB_wzVO_yn7d3_1cflmsvj98Xd6uFqZQRVw0qpZMGopN3bCCbgALWdfAoGZFtZGVpE1hRNPksqKM1owLrBly0RQVRSZycZV9POmO82bA2qCLE_R6nOwA0157sPp_xNlOt36nleAFK2USeP8kMPnfM4aoBxsM9j049HPQXEpVSMarMlGvT9T0zhAmbM5rGNWHfHTKRx_zSdx3__o6M_8GkggPJ0JCrYHeu9461Fs_T-m3g8Y_Ze2HPWhOOdOUckVVaukoKVPJmVA5Zexg69NJaRtiyvG8CqZoTY9HU1xpdShHc2fEdDBpdOIRsB265w</recordid><startdate>20210801</startdate><enddate>20210801</enddate><creator>Yoshii, Daiki</creator><creator>Nakagawa, Takenobu</creator><creator>Komohara, Yoshihiro</creator><creator>Kawaguchi, Hiroaki</creator><creator>Yamada, Sohsuke</creator><creator>Tanimoto, Akihide</creator><general>Japan Atherosclerosis Society</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>5PM</scope></search><sort><creationdate>20210801</creationdate><title>Phenotypic Changes in Macrophage Activation in a Model of Nonalcoholic Fatty Liver Disease using Microminipigs</title><author>Yoshii, Daiki ; Nakagawa, Takenobu ; Komohara, Yoshihiro ; Kawaguchi, Hiroaki ; Yamada, Sohsuke ; Tanimoto, Akihide</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c686t-f8d414c0efdf160bae64dda1ad169b4940f6c3ff549010d123ed1e23f690e1353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Antigens, CD - metabolism</topic><topic>Antigens, Differentiation, Myelomonocytic - metabolism</topic><topic>Cholesterol - administration & dosage</topic><topic>Cholesterol - toxicity</topic><topic>Cholic Acid - administration & dosage</topic><topic>Cholic Acid - toxicity</topic><topic>Diet, High-Fat</topic><topic>Disease Models, Animal</topic><topic>Disease Progression</topic><topic>Fatty liver disease</topic><topic>Hepatic Stellate Cells - immunology</topic><topic>Hepatic Stellate Cells - metabolism</topic><topic>Hepatic Stellate Cells - pathology</topic><topic>Lymphocytes - immunology</topic><topic>Lymphocytes - metabolism</topic><topic>Lymphocytes - pathology</topic><topic>Macrophage</topic><topic>Macrophage Activation - immunology</topic><topic>Macrophages - immunology</topic><topic>Macrophages - metabolism</topic><topic>Macrophages - pathology</topic><topic>Microminipig</topic><topic>NAFLD</topic><topic>NASH</topic><topic>Non-alcoholic Fatty Liver Disease - chemically induced</topic><topic>Non-alcoholic Fatty Liver Disease - immunology</topic><topic>Non-alcoholic Fatty Liver Disease - pathology</topic><topic>Original</topic><topic>Phenotype</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Swine</topic><topic>Swine, Miniature</topic><toplevel>online_resources</toplevel><creatorcontrib>Yoshii, Daiki</creatorcontrib><creatorcontrib>Nakagawa, Takenobu</creatorcontrib><creatorcontrib>Komohara, Yoshihiro</creatorcontrib><creatorcontrib>Kawaguchi, Hiroaki</creatorcontrib><creatorcontrib>Yamada, Sohsuke</creatorcontrib><creatorcontrib>Tanimoto, Akihide</creatorcontrib><creatorcontrib>Department of Pathology</creatorcontrib><creatorcontrib>Department of Pathology and Laboratory Medicine</creatorcontrib><creatorcontrib>Kumamoto University</creatorcontrib><creatorcontrib>Kanazawa Medical University</creatorcontrib><creatorcontrib>Center for Metabolic Regulation of Healthy Aging</creatorcontrib><creatorcontrib>Department of Cell Pathology</creatorcontrib><creatorcontrib>Department of Hygiene and Health Promotion Medicine</creatorcontrib><creatorcontrib>Kagoshima University Graduate School of Medical and Dental Sciences</creatorcontrib><creatorcontrib>Graduate School of Medical Sciences</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>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yoshii, Daiki</au><au>Nakagawa, Takenobu</au><au>Komohara, Yoshihiro</au><au>Kawaguchi, Hiroaki</au><au>Yamada, Sohsuke</au><au>Tanimoto, Akihide</au><aucorp>Department of Pathology</aucorp><aucorp>Department of Pathology and Laboratory Medicine</aucorp><aucorp>Kumamoto University</aucorp><aucorp>Kanazawa Medical University</aucorp><aucorp>Center for Metabolic Regulation of Healthy Aging</aucorp><aucorp>Department of Cell Pathology</aucorp><aucorp>Department of Hygiene and Health Promotion Medicine</aucorp><aucorp>Kagoshima University Graduate School of Medical and Dental Sciences</aucorp><aucorp>Graduate School of Medical Sciences</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenotypic Changes in Macrophage Activation in a Model of Nonalcoholic Fatty Liver Disease using Microminipigs</atitle><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle><addtitle>JAT</addtitle><date>2021-08-01</date><risdate>2021</risdate><volume>28</volume><issue>8</issue><spage>844</spage><epage>851</epage><pages>844-851</pages><artnum>57703</artnum><issn>1340-3478</issn><eissn>1880-3873</eissn><abstract>Aim: Non-alcoholic fatty liver disease (NAFLD) is one of the most common chronic liver disorders associated with metabolic syndrome, and its prevalence has been on the rise. The pathogenesis of NAFLD has not yet been sufficiently elucidated due to the multifactorial nature of the disease, although the activation of macrophages/Kupffer cells is considered to be involved. We previously reported an animal model of NAFLD using MicrominipigsTM (µMPs) fed high-fat diets containing cholesterol with or without cholic acid. The aim of this study was to investigate the phenotypic changes of macrophages that occur during the development of NAFLD. Methods: Immunohistochemistry of macrophages, lymphocytes, and stellate cells was performed using liver samples, and the density of positive cells was analyzed. Results: The number of Iba-1-positive macrophages increased with increasing cholesterol content in the diet. The numbers of CD163-positive macrophages and CD204-positive macrophages also increased with increasing cholesterol content in the diet; however, the proportion of CD204-positive macrophages among Iba-1-positive macrophages was significantly reduced by cholic acid supplementation. Conclusion: The results suggest that lipid accumulation induced macrophage recruitment in swine livers, and that the number of M2-like macrophages increased at the early stage of NAFLD, while the number of M1-like macrophages increased at the late stage of NAFLD, resulting in a liver condition like non-alcoholic steatohepatitis. We provide evidence of the phenotypic changes that occur in macrophages during the development of NAFLD that has never been reported before using µMPs.</abstract><cop>Japan</cop><pub>Japan Atherosclerosis Society</pub><pmid>33012740</pmid><doi>10.5551/jat.57703</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antigens, CD - metabolism Antigens, Differentiation, Myelomonocytic - metabolism Cholesterol - administration & dosage Cholesterol - toxicity Cholic Acid - administration & dosage Cholic Acid - toxicity Diet, High-Fat Disease Models, Animal Disease Progression Fatty liver disease Hepatic Stellate Cells - immunology Hepatic Stellate Cells - metabolism Hepatic Stellate Cells - pathology Lymphocytes - immunology Lymphocytes - metabolism Lymphocytes - pathology Macrophage Macrophage Activation - immunology Macrophages - immunology Macrophages - metabolism Macrophages - pathology Microminipig NAFLD NASH Non-alcoholic Fatty Liver Disease - chemically induced Non-alcoholic Fatty Liver Disease - immunology Non-alcoholic Fatty Liver Disease - pathology Original Phenotype Receptors, Cell Surface - metabolism Swine Swine, Miniature |
title | Phenotypic Changes in Macrophage Activation in a Model of Nonalcoholic Fatty Liver Disease using Microminipigs |
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