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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
Main Authors: 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
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container_title Atherosclerosis
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creator 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
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&amp;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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ispartof Atherosclerosis, 2009-12, Vol.207 (2), p.360-367
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1879-1484
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source ScienceDirect Journals
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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