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Atherosclerotic mice exhibit systemic inflammation in periadventitial and visceral adipose tissue, liver, and pancreatic islets
Abstract Objective Atherosclerosis is a chronic inflammatory disease of major conduit arteries. Similarly, obesity and type 2 diabetes mellitus are associated with accumulation of macrophages in visceral white adipose tissue and pancreatic islets. Our goal was to characterize systemic inflammation i...
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Published in: | Atherosclerosis 2009-12, Vol.207 (2), p.360-367 |
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description | Abstract Objective Atherosclerosis is a chronic inflammatory disease of major conduit arteries. Similarly, obesity and type 2 diabetes mellitus are associated with accumulation of macrophages in visceral white adipose tissue and pancreatic islets. Our goal was to characterize systemic inflammation in atherosclerosis with hypercholesterolemia, but without obesity. Methods and results We compared 22-week-old apolipoprotein E knockout ( ApoE−/− ) with wild-type mice kept for 14 weeks on a high cholesterol (1.25%) diet (CD, n = 8) and 8-week-old ApoE−/− with wild-type mice kept on a normal diet (ND, n = 8). Hypercholesterolemic, atherosclerotic ApoE−/− mice on CD exhibited increased macrophages and T-cells in plaques and periadventitial adipose tissue that revealed elevated expression of MIP-1α , IL-1β , IL-1 receptor , and IL-6 . Mesenteric adipose tissue and pancreatic islets in ApoE−/− mice showed increased macrophages. Expression of IL-1β was enhanced in mesenteric adipose tissue of ApoE−/− mice on CD. Furthermore, these mice exhibited steatohepatitis with macrophage and T-cell infiltrations as well as increased MIP-1α and IL-1 receptor expression. Blood glucose, insulin and total body weight did not differ between the groups. Conclusions In hypercholesterolemic lean ApoE−/− mice, inflammation extends beyond atherosclerotic plaques to the periadventitial and visceral adipose tissue, liver, and pancreatic islets without affecting glucose homeostasis. |
doi_str_mv | 10.1016/j.atherosclerosis.2009.05.004 |
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Similarly, obesity and type 2 diabetes mellitus are associated with accumulation of macrophages in visceral white adipose tissue and pancreatic islets. Our goal was to characterize systemic inflammation in atherosclerosis with hypercholesterolemia, but without obesity. Methods and results We compared 22-week-old apolipoprotein E knockout ( ApoE−/− ) with wild-type mice kept for 14 weeks on a high cholesterol (1.25%) diet (CD, n = 8) and 8-week-old ApoE−/− with wild-type mice kept on a normal diet (ND, n = 8). Hypercholesterolemic, atherosclerotic ApoE−/− mice on CD exhibited increased macrophages and T-cells in plaques and periadventitial adipose tissue that revealed elevated expression of MIP-1α , IL-1β , IL-1 receptor , and IL-6 . Mesenteric adipose tissue and pancreatic islets in ApoE−/− mice showed increased macrophages. Expression of IL-1β was enhanced in mesenteric adipose tissue of ApoE−/− mice on CD. Furthermore, these mice exhibited steatohepatitis with macrophage and T-cell infiltrations as well as increased MIP-1α and IL-1 receptor expression. Blood glucose, insulin and total body weight did not differ between the groups. Conclusions In hypercholesterolemic lean ApoE−/− mice, inflammation extends beyond atherosclerotic plaques to the periadventitial and visceral adipose tissue, liver, and pancreatic islets without affecting glucose homeostasis.</description><identifier>ISSN: 0021-9150</identifier><identifier>ISSN: 1879-1484</identifier><identifier>EISSN: 1879-1484</identifier><identifier>DOI: 10.1016/j.atherosclerosis.2009.05.004</identifier><identifier>PMID: 19481752</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ireland Ltd</publisher><subject>Adipose tissue ; Animals ; Apolipoproteins E - deficiency ; Apolipoproteins E - genetics ; Atherosclerosis ; Atherosclerosis (general aspects, experimental research) ; Atherosclerosis - genetics ; Atherosclerosis - immunology ; Atherosclerosis - pathology ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood Glucose - metabolism ; Body Weight ; Cardiology. Vascular system ; Cardiovascular ; Connective Tissue - immunology ; Connective Tissue - pathology ; Cytokines - blood ; Disease Models, Animal ; Fatty Liver - immunology ; Fatty Liver - pathology ; Hypercholesterolemia ; Hypercholesterolemia - complications ; Hypercholesterolemia - genetics ; Hypercholesterolemia - immunology ; Hypercholesterolemia - pathology ; Immunomodulators ; Inflammation - genetics ; Inflammation - immunology ; Inflammation - pathology ; Inflammation Mediators - blood ; Insulin - blood ; Intra-Abdominal Fat - immunology ; Intra-Abdominal Fat - pathology ; Islets of Langerhans - immunology ; Islets of Langerhans - pathology ; Liver - immunology ; Liver - pathology ; Macrophages ; Macrophages - immunology ; Male ; MEDICAL AND HEALTH SCIENCES ; Medical sciences ; MEDICIN OCH HÄLSOVETENSKAP ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Pancreatic islets ; Pharmacology. Drug treatments ; T-Lymphocytes - immunology</subject><ispartof>Atherosclerosis, 2009-12, Vol.207 (2), p.360-367</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2009 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c510t-42e1a7e59de7beed3416db3e8f09dc019546ceff32425de3fdc0276dc8f600233</citedby><cites>FETCH-LOGICAL-c510t-42e1a7e59de7beed3416db3e8f09dc019546ceff32425de3fdc0276dc8f600233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22366763$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19481752$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://gup.ub.gu.se/publication/95488$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Lohmann, Christine</creatorcontrib><creatorcontrib>Schäfer, Nicola</creatorcontrib><creatorcontrib>von Lukowicz, Tobias</creatorcontrib><creatorcontrib>Sokrates Stein, M.A</creatorcontrib><creatorcontrib>Borén, Jan</creatorcontrib><creatorcontrib>Rütti, Sabine</creatorcontrib><creatorcontrib>Wahli, Walter</creatorcontrib><creatorcontrib>Donath, Marc Y</creatorcontrib><creatorcontrib>Lüscher, Thomas F</creatorcontrib><creatorcontrib>Matter, Christian M</creatorcontrib><title>Atherosclerotic mice exhibit systemic inflammation in periadventitial and visceral adipose tissue, liver, and pancreatic islets</title><title>Atherosclerosis</title><addtitle>Atherosclerosis</addtitle><description>Abstract Objective Atherosclerosis is a chronic inflammatory disease of major conduit arteries. Similarly, obesity and type 2 diabetes mellitus are associated with accumulation of macrophages in visceral white adipose tissue and pancreatic islets. Our goal was to characterize systemic inflammation in atherosclerosis with hypercholesterolemia, but without obesity. Methods and results We compared 22-week-old apolipoprotein E knockout ( ApoE−/− ) with wild-type mice kept for 14 weeks on a high cholesterol (1.25%) diet (CD, n = 8) and 8-week-old ApoE−/− with wild-type mice kept on a normal diet (ND, n = 8). Hypercholesterolemic, atherosclerotic ApoE−/− mice on CD exhibited increased macrophages and T-cells in plaques and periadventitial adipose tissue that revealed elevated expression of MIP-1α , IL-1β , IL-1 receptor , and IL-6 . Mesenteric adipose tissue and pancreatic islets in ApoE−/− mice showed increased macrophages. Expression of IL-1β was enhanced in mesenteric adipose tissue of ApoE−/− mice on CD. Furthermore, these mice exhibited steatohepatitis with macrophage and T-cell infiltrations as well as increased MIP-1α and IL-1 receptor expression. Blood glucose, insulin and total body weight did not differ between the groups. Conclusions In hypercholesterolemic lean ApoE−/− mice, inflammation extends beyond atherosclerotic plaques to the periadventitial and visceral adipose tissue, liver, and pancreatic islets without affecting glucose homeostasis.</description><subject>Adipose tissue</subject><subject>Animals</subject><subject>Apolipoproteins E - deficiency</subject><subject>Apolipoproteins E - genetics</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Atherosclerosis - genetics</subject><subject>Atherosclerosis - immunology</subject><subject>Atherosclerosis - pathology</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood Glucose - metabolism</subject><subject>Body Weight</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Connective Tissue - immunology</subject><subject>Connective Tissue - pathology</subject><subject>Cytokines - blood</subject><subject>Disease Models, Animal</subject><subject>Fatty Liver - immunology</subject><subject>Fatty Liver - pathology</subject><subject>Hypercholesterolemia</subject><subject>Hypercholesterolemia - complications</subject><subject>Hypercholesterolemia - genetics</subject><subject>Hypercholesterolemia - immunology</subject><subject>Hypercholesterolemia - pathology</subject><subject>Immunomodulators</subject><subject>Inflammation - genetics</subject><subject>Inflammation - immunology</subject><subject>Inflammation - pathology</subject><subject>Inflammation Mediators - blood</subject><subject>Insulin - blood</subject><subject>Intra-Abdominal Fat - immunology</subject><subject>Intra-Abdominal Fat - pathology</subject><subject>Islets of Langerhans - immunology</subject><subject>Islets of Langerhans - pathology</subject><subject>Liver - immunology</subject><subject>Liver - pathology</subject><subject>Macrophages</subject><subject>Macrophages - immunology</subject><subject>Male</subject><subject>MEDICAL AND HEALTH SCIENCES</subject><subject>Medical sciences</subject><subject>MEDICIN OCH HÄLSOVETENSKAP</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Pancreatic islets</subject><subject>Pharmacology. Drug treatments</subject><subject>T-Lymphocytes - immunology</subject><issn>0021-9150</issn><issn>1879-1484</issn><issn>1879-1484</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNkktv1DAQxyMEokvhK6BcKi6bMM47B5CqCgpSJQ7A2XLsSTuL88DjLOyJr47DLg_1xMWWRz__5_GfKLoQkAoQ1ctdqvwduom1XU_iNANoUyhTgOJBtBFN3SaiaIqH0QYgE0krSjiLnjDvIBC1aB5HZ6ItGlGX2Sb6cfmPmicdD6Qxxu931JGP-cAeQySmsbdqGJSnaQyPeEZHyuxx9ORJ2ViNJt4Ta3Trw9A8McaemBfcxpb26La_mFmN2qFaExFb9Pw0etQry_jsdJ9Hn9---XT1Lrn5cP3-6vIm0aUAnxQZClVj2RqsO0STF6IyXY5ND63RINqyqDT2fZ4VWWkw70Mwqyujm74KU8jz82h71OVvOC-dnB0Nyh3kpEjeLrMModtFMsqg1DQBf3HEZzd9XZC9HNburFUjTgvLOhRQtk0BgXx1JHWYIjvs_0gLkKtjcifvOSZXxySUMvgR_j8_ZVq6Ac3f3yeLAnBxAhRrZXsXRhg0fnNZlldVXa0dXh85DGPcEzrJmnDUaMih9tJM9N8lvb6npC2NFJJ_wQPyblrcGLySQnImQX5c12zdMmgB8ryt8p-EoNeQ</recordid><startdate>20091201</startdate><enddate>20091201</enddate><creator>Lohmann, Christine</creator><creator>Schäfer, Nicola</creator><creator>von Lukowicz, Tobias</creator><creator>Sokrates Stein, M.A</creator><creator>Borén, Jan</creator><creator>Rütti, Sabine</creator><creator>Wahli, Walter</creator><creator>Donath, Marc Y</creator><creator>Lüscher, Thomas F</creator><creator>Matter, Christian M</creator><general>Elsevier Ireland Ltd</general><general>Elsevier</general><scope>IQODW</scope><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>ADTPV</scope><scope>AOWAS</scope><scope>F1U</scope></search><sort><creationdate>20091201</creationdate><title>Atherosclerotic mice exhibit systemic inflammation in periadventitial and visceral adipose tissue, liver, and pancreatic islets</title><author>Lohmann, Christine ; Schäfer, Nicola ; von Lukowicz, Tobias ; Sokrates Stein, M.A ; Borén, Jan ; Rütti, Sabine ; Wahli, Walter ; Donath, Marc Y ; Lüscher, Thomas F ; Matter, Christian M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c510t-42e1a7e59de7beed3416db3e8f09dc019546ceff32425de3fdc0276dc8f600233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adipose tissue</topic><topic>Animals</topic><topic>Apolipoproteins E - deficiency</topic><topic>Apolipoproteins E - genetics</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Atherosclerosis - genetics</topic><topic>Atherosclerosis - immunology</topic><topic>Atherosclerosis - pathology</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood Glucose - metabolism</topic><topic>Body Weight</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular</topic><topic>Connective Tissue - immunology</topic><topic>Connective Tissue - pathology</topic><topic>Cytokines - blood</topic><topic>Disease Models, Animal</topic><topic>Fatty Liver - immunology</topic><topic>Fatty Liver - pathology</topic><topic>Hypercholesterolemia</topic><topic>Hypercholesterolemia - complications</topic><topic>Hypercholesterolemia - genetics</topic><topic>Hypercholesterolemia - immunology</topic><topic>Hypercholesterolemia - pathology</topic><topic>Immunomodulators</topic><topic>Inflammation - genetics</topic><topic>Inflammation - immunology</topic><topic>Inflammation - pathology</topic><topic>Inflammation Mediators - blood</topic><topic>Insulin - blood</topic><topic>Intra-Abdominal Fat - immunology</topic><topic>Intra-Abdominal Fat - pathology</topic><topic>Islets of Langerhans - immunology</topic><topic>Islets of Langerhans - pathology</topic><topic>Liver - immunology</topic><topic>Liver - pathology</topic><topic>Macrophages</topic><topic>Macrophages - immunology</topic><topic>Male</topic><topic>MEDICAL AND HEALTH SCIENCES</topic><topic>Medical sciences</topic><topic>MEDICIN OCH HÄLSOVETENSKAP</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Pancreatic islets</topic><topic>Pharmacology. Drug treatments</topic><topic>T-Lymphocytes - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lohmann, Christine</creatorcontrib><creatorcontrib>Schäfer, Nicola</creatorcontrib><creatorcontrib>von Lukowicz, Tobias</creatorcontrib><creatorcontrib>Sokrates Stein, M.A</creatorcontrib><creatorcontrib>Borén, Jan</creatorcontrib><creatorcontrib>Rütti, Sabine</creatorcontrib><creatorcontrib>Wahli, Walter</creatorcontrib><creatorcontrib>Donath, Marc Y</creatorcontrib><creatorcontrib>Lüscher, Thomas F</creatorcontrib><creatorcontrib>Matter, Christian M</creatorcontrib><collection>Pascal-Francis</collection><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>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Göteborgs universitet</collection><jtitle>Atherosclerosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lohmann, Christine</au><au>Schäfer, Nicola</au><au>von Lukowicz, Tobias</au><au>Sokrates Stein, M.A</au><au>Borén, Jan</au><au>Rütti, Sabine</au><au>Wahli, Walter</au><au>Donath, Marc Y</au><au>Lüscher, Thomas F</au><au>Matter, Christian M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Atherosclerotic mice exhibit systemic inflammation in periadventitial and visceral adipose tissue, liver, and pancreatic islets</atitle><jtitle>Atherosclerosis</jtitle><addtitle>Atherosclerosis</addtitle><date>2009-12-01</date><risdate>2009</risdate><volume>207</volume><issue>2</issue><spage>360</spage><epage>367</epage><pages>360-367</pages><issn>0021-9150</issn><issn>1879-1484</issn><eissn>1879-1484</eissn><abstract>Abstract Objective Atherosclerosis is a chronic inflammatory disease of major conduit arteries. Similarly, obesity and type 2 diabetes mellitus are associated with accumulation of macrophages in visceral white adipose tissue and pancreatic islets. Our goal was to characterize systemic inflammation in atherosclerosis with hypercholesterolemia, but without obesity. Methods and results We compared 22-week-old apolipoprotein E knockout ( ApoE−/− ) with wild-type mice kept for 14 weeks on a high cholesterol (1.25%) diet (CD, n = 8) and 8-week-old ApoE−/− with wild-type mice kept on a normal diet (ND, n = 8). Hypercholesterolemic, atherosclerotic ApoE−/− mice on CD exhibited increased macrophages and T-cells in plaques and periadventitial adipose tissue that revealed elevated expression of MIP-1α , IL-1β , IL-1 receptor , and IL-6 . Mesenteric adipose tissue and pancreatic islets in ApoE−/− mice showed increased macrophages. Expression of IL-1β was enhanced in mesenteric adipose tissue of ApoE−/− mice on CD. Furthermore, these mice exhibited steatohepatitis with macrophage and T-cell infiltrations as well as increased MIP-1α and IL-1 receptor expression. Blood glucose, insulin and total body weight did not differ between the groups. Conclusions In hypercholesterolemic lean ApoE−/− mice, inflammation extends beyond atherosclerotic plaques to the periadventitial and visceral adipose tissue, liver, and pancreatic islets without affecting glucose homeostasis.</abstract><cop>Amsterdam</cop><pub>Elsevier Ireland Ltd</pub><pmid>19481752</pmid><doi>10.1016/j.atherosclerosis.2009.05.004</doi><tpages>8</tpages></addata></record> |
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subjects | Adipose tissue Animals Apolipoproteins E - deficiency Apolipoproteins E - genetics Atherosclerosis Atherosclerosis (general aspects, experimental research) Atherosclerosis - genetics Atherosclerosis - immunology Atherosclerosis - pathology Biological and medical sciences Blood and lymphatic vessels Blood Glucose - metabolism Body Weight Cardiology. Vascular system Cardiovascular Connective Tissue - immunology Connective Tissue - pathology Cytokines - blood Disease Models, Animal Fatty Liver - immunology Fatty Liver - pathology Hypercholesterolemia Hypercholesterolemia - complications Hypercholesterolemia - genetics Hypercholesterolemia - immunology Hypercholesterolemia - pathology Immunomodulators Inflammation - genetics Inflammation - immunology Inflammation - pathology Inflammation Mediators - blood Insulin - blood Intra-Abdominal Fat - immunology Intra-Abdominal Fat - pathology Islets of Langerhans - immunology Islets of Langerhans - pathology Liver - immunology Liver - pathology Macrophages Macrophages - immunology Male MEDICAL AND HEALTH SCIENCES Medical sciences MEDICIN OCH HÄLSOVETENSKAP Mice Mice, Inbred C57BL Mice, Knockout Pancreatic islets Pharmacology. Drug treatments T-Lymphocytes - immunology |
title | Atherosclerotic mice exhibit systemic inflammation in periadventitial and visceral adipose tissue, liver, and pancreatic islets |
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