Antagonism of RANTES Receptors Reduces Atherosclerotic Plaque Formation in Mice
ABSTRACT—Increasing evidence supports the involvement of inflammation in the early phases of atherogenesis. Recruitment of leukocytes within the vascular wall, controlled by chemokines, is an essential process in the development of this common disease. In this study, we report that blocking a chemok...
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Veröffentlicht in: | Circulation research 2004-02, Vol.94 (2), p.253-261 |
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description | ABSTRACT—Increasing evidence supports the involvement of inflammation in the early phases of atherogenesis. Recruitment of leukocytes within the vascular wall, controlled by chemokines, is an essential process in the development of this common disease. In this study, we report that blocking a chemokine pathway in vivo with the CC chemokine antagonist Met-RANTES reduces the progression of atherosclerosis in a hypercholesterolemic mouse model. The reduction of lesions was correlated with a diminution of expression of several major chemokines and chemokine receptors, a decrease in leukocyte infiltration, and an increase of collagen-rich atheroma, features associated with stable atheroma. Treatment was well tolerated and serum lipid profiles were not affected. Whereas genetically engineered mice with deletion of either a CC chemokine or its receptor have demonstrated resistance to disease, to our knowledge, this is the first demonstration that treatment with a chemokine receptor antagonist limits the progression of atherosclerosis in vivo. Thus, our findings indicate that blockade of chemokine receptor/ligand interactions might become a novel therapeutic strategy to reduce the evolution of this common disease. |
doi_str_mv | 10.1161/01.RES.0000109793.17591.4E |
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Recruitment of leukocytes within the vascular wall, controlled by chemokines, is an essential process in the development of this common disease. In this study, we report that blocking a chemokine pathway in vivo with the CC chemokine antagonist Met-RANTES reduces the progression of atherosclerosis in a hypercholesterolemic mouse model. The reduction of lesions was correlated with a diminution of expression of several major chemokines and chemokine receptors, a decrease in leukocyte infiltration, and an increase of collagen-rich atheroma, features associated with stable atheroma. Treatment was well tolerated and serum lipid profiles were not affected. Whereas genetically engineered mice with deletion of either a CC chemokine or its receptor have demonstrated resistance to disease, to our knowledge, this is the first demonstration that treatment with a chemokine receptor antagonist limits the progression of atherosclerosis in vivo. Thus, our findings indicate that blockade of chemokine receptor/ligand interactions might become a novel therapeutic strategy to reduce the evolution of this common disease.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/01.RES.0000109793.17591.4E</identifier><identifier>PMID: 14656931</identifier><identifier>CODEN: CIRUAL</identifier><language>eng</language><publisher>Hagerstown, MD: American Heart Association, Inc</publisher><subject>Animals ; Aorta - drug effects ; Aorta - pathology ; Apolipoproteins E - deficiency ; Apolipoproteins E - genetics ; Arteriosclerosis - pathology ; Arteriosclerosis - prevention & control ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; CCR5 Receptor Antagonists ; Chemokine CCL5 - analogs & derivatives ; Chemokine CCL5 - metabolism ; Chemokine CCL5 - pharmacology ; Chemokines - biosynthesis ; Chemokines - genetics ; Chemotaxis, Leukocyte - drug effects ; Cholesterol, Dietary - toxicity ; Endothelium, Vascular - metabolism ; Endothelium, Vascular - pathology ; Fundamental and applied biological sciences. Psychology ; Gene Expression Regulation - drug effects ; Male ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Protein Binding ; Receptors, CCR1 ; Receptors, CCR2 ; Receptors, CCR5 - physiology ; Receptors, Chemokine - antagonists & inhibitors ; Receptors, Chemokine - biosynthesis ; Receptors, Chemokine - deficiency ; Receptors, Chemokine - drug effects ; Receptors, Chemokine - genetics ; Receptors, Chemokine - physiology ; Receptors, LDL - deficiency ; RNA, Messenger - genetics ; Vasculitis - pathology ; Vasculitis - prevention & control ; Vertebrates: cardiovascular system</subject><ispartof>Circulation research, 2004-02, Vol.94 (2), p.253-261</ispartof><rights>2004 American Heart Association, Inc.</rights><rights>2004 INIST-CNRS</rights><rights>Copyright American Heart Association, Inc. 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Recruitment of leukocytes within the vascular wall, controlled by chemokines, is an essential process in the development of this common disease. In this study, we report that blocking a chemokine pathway in vivo with the CC chemokine antagonist Met-RANTES reduces the progression of atherosclerosis in a hypercholesterolemic mouse model. The reduction of lesions was correlated with a diminution of expression of several major chemokines and chemokine receptors, a decrease in leukocyte infiltration, and an increase of collagen-rich atheroma, features associated with stable atheroma. Treatment was well tolerated and serum lipid profiles were not affected. Whereas genetically engineered mice with deletion of either a CC chemokine or its receptor have demonstrated resistance to disease, to our knowledge, this is the first demonstration that treatment with a chemokine receptor antagonist limits the progression of atherosclerosis in vivo. Thus, our findings indicate that blockade of chemokine receptor/ligand interactions might become a novel therapeutic strategy to reduce the evolution of this common disease.</description><subject>Animals</subject><subject>Aorta - drug effects</subject><subject>Aorta - pathology</subject><subject>Apolipoproteins E - deficiency</subject><subject>Apolipoproteins E - genetics</subject><subject>Arteriosclerosis - pathology</subject><subject>Arteriosclerosis - prevention & control</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>CCR5 Receptor Antagonists</subject><subject>Chemokine CCL5 - analogs & derivatives</subject><subject>Chemokine CCL5 - metabolism</subject><subject>Chemokine CCL5 - pharmacology</subject><subject>Chemokines - biosynthesis</subject><subject>Chemokines - genetics</subject><subject>Chemotaxis, Leukocyte - drug effects</subject><subject>Cholesterol, Dietary - toxicity</subject><subject>Endothelium, Vascular - metabolism</subject><subject>Endothelium, Vascular - pathology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gene Expression Regulation - drug effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Protein Binding</subject><subject>Receptors, CCR1</subject><subject>Receptors, CCR2</subject><subject>Receptors, CCR5 - physiology</subject><subject>Receptors, Chemokine - antagonists & inhibitors</subject><subject>Receptors, Chemokine - biosynthesis</subject><subject>Receptors, Chemokine - deficiency</subject><subject>Receptors, Chemokine - drug effects</subject><subject>Receptors, Chemokine - genetics</subject><subject>Receptors, Chemokine - physiology</subject><subject>Receptors, LDL - deficiency</subject><subject>RNA, Messenger - genetics</subject><subject>Vasculitis - pathology</subject><subject>Vasculitis - prevention & control</subject><subject>Vertebrates: cardiovascular system</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkF1v2yAUhtG0ac3a_YXJqrRLuxzAEHYXVW43qR9T2l4jDIfFnWNnYKvqvx9tIuVcABfP4X31EHIOtAKQcEGhWjcPFc0DVCvNK1C1hko0H8gCaiZKUSv4SBYZ0KXinJ6QLyk9Z1xwpj-TExCylprDgtyvhsn-GYcubYsxFOvV3WPzUKzR4W4aY8ovPztMxWraYByT6_M5da743dt_MxZXY9zaqRuHohuK287hGfkUbJ_w6-E-JU9XzePlz_Lm_vrX5eqmdHJZ65IxplgI1oe2ZbRFq4TXVoAVXIJjLbcKPQpkQQclcYlaBuk89d5zqZaOn5Lz_b-7OOYiaTLP4xyHHGkYMMG0ApWhH3vI5eopYjC72G1tfDVAzZtKQ8Fkleao0ryrNKLJy98OCXO7RX9cPbjLwPcDYJOzfYh2cF06cnUeyljmxJ57GfsJY_rbzy8YzQZtP23eozkFVjJKBWVU0vKtjOb_Ab0AjDo</recordid><startdate>20040206</startdate><enddate>20040206</enddate><creator>Veillard, Niels R</creator><creator>Kwak, Brenda</creator><creator>Pelli, Graziano</creator><creator>Mulhaupt, Flore</creator><creator>James, Richard W</creator><creator>Proudfoot, Amanda E.I</creator><creator>Mach, François</creator><general>American Heart Association, Inc</general><general>Lippincott</general><general>Lippincott Williams & Wilkins Ovid Technologies</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>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope><scope>K9.</scope></search><sort><creationdate>20040206</creationdate><title>Antagonism of RANTES Receptors Reduces Atherosclerotic Plaque Formation in Mice</title><author>Veillard, Niels R ; Kwak, Brenda ; Pelli, Graziano ; Mulhaupt, Flore ; James, Richard W ; Proudfoot, Amanda E.I ; Mach, François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6859-22272ffadfbb20bea74d9a41a4361c2b3a7ede4e2f9f76e8e96f6cd0ddd3678c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Aorta - drug effects</topic><topic>Aorta - pathology</topic><topic>Apolipoproteins E - deficiency</topic><topic>Apolipoproteins E - genetics</topic><topic>Arteriosclerosis - pathology</topic><topic>Arteriosclerosis - prevention & control</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>CCR5 Receptor Antagonists</topic><topic>Chemokine CCL5 - analogs & derivatives</topic><topic>Chemokine CCL5 - metabolism</topic><topic>Chemokine CCL5 - pharmacology</topic><topic>Chemokines - biosynthesis</topic><topic>Chemokines - genetics</topic><topic>Chemotaxis, Leukocyte - drug effects</topic><topic>Cholesterol, Dietary - toxicity</topic><topic>Endothelium, Vascular - metabolism</topic><topic>Endothelium, Vascular - pathology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gene Expression Regulation - drug effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Protein Binding</topic><topic>Receptors, CCR1</topic><topic>Receptors, CCR2</topic><topic>Receptors, CCR5 - physiology</topic><topic>Receptors, Chemokine - antagonists & inhibitors</topic><topic>Receptors, Chemokine - biosynthesis</topic><topic>Receptors, Chemokine - deficiency</topic><topic>Receptors, Chemokine - drug effects</topic><topic>Receptors, Chemokine - genetics</topic><topic>Receptors, Chemokine - physiology</topic><topic>Receptors, LDL - deficiency</topic><topic>RNA, Messenger - genetics</topic><topic>Vasculitis - pathology</topic><topic>Vasculitis - prevention & control</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Veillard, Niels R</creatorcontrib><creatorcontrib>Kwak, Brenda</creatorcontrib><creatorcontrib>Pelli, Graziano</creatorcontrib><creatorcontrib>Mulhaupt, Flore</creatorcontrib><creatorcontrib>James, Richard W</creatorcontrib><creatorcontrib>Proudfoot, Amanda E.I</creatorcontrib><creatorcontrib>Mach, François</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>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Veillard, Niels R</au><au>Kwak, Brenda</au><au>Pelli, Graziano</au><au>Mulhaupt, Flore</au><au>James, Richard W</au><au>Proudfoot, Amanda E.I</au><au>Mach, François</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antagonism of RANTES Receptors Reduces Atherosclerotic Plaque Formation in Mice</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2004-02-06</date><risdate>2004</risdate><volume>94</volume><issue>2</issue><spage>253</spage><epage>261</epage><pages>253-261</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>ABSTRACT—Increasing evidence supports the involvement of inflammation in the early phases of atherogenesis. Recruitment of leukocytes within the vascular wall, controlled by chemokines, is an essential process in the development of this common disease. In this study, we report that blocking a chemokine pathway in vivo with the CC chemokine antagonist Met-RANTES reduces the progression of atherosclerosis in a hypercholesterolemic mouse model. The reduction of lesions was correlated with a diminution of expression of several major chemokines and chemokine receptors, a decrease in leukocyte infiltration, and an increase of collagen-rich atheroma, features associated with stable atheroma. Treatment was well tolerated and serum lipid profiles were not affected. Whereas genetically engineered mice with deletion of either a CC chemokine or its receptor have demonstrated resistance to disease, to our knowledge, this is the first demonstration that treatment with a chemokine receptor antagonist limits the progression of atherosclerosis in vivo. Thus, our findings indicate that blockade of chemokine receptor/ligand interactions might become a novel therapeutic strategy to reduce the evolution of this common disease.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>14656931</pmid><doi>10.1161/01.RES.0000109793.17591.4E</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Aorta - drug effects Aorta - pathology Apolipoproteins E - deficiency Apolipoproteins E - genetics Arteriosclerosis - pathology Arteriosclerosis - prevention & control Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system CCR5 Receptor Antagonists Chemokine CCL5 - analogs & derivatives Chemokine CCL5 - metabolism Chemokine CCL5 - pharmacology Chemokines - biosynthesis Chemokines - genetics Chemotaxis, Leukocyte - drug effects Cholesterol, Dietary - toxicity Endothelium, Vascular - metabolism Endothelium, Vascular - pathology Fundamental and applied biological sciences. Psychology Gene Expression Regulation - drug effects Male Medical sciences Mice Mice, Inbred C57BL Mice, Knockout Protein Binding Receptors, CCR1 Receptors, CCR2 Receptors, CCR5 - physiology Receptors, Chemokine - antagonists & inhibitors Receptors, Chemokine - biosynthesis Receptors, Chemokine - deficiency Receptors, Chemokine - drug effects Receptors, Chemokine - genetics Receptors, Chemokine - physiology Receptors, LDL - deficiency RNA, Messenger - genetics Vasculitis - pathology Vasculitis - prevention & control Vertebrates: cardiovascular system |
title | Antagonism of RANTES Receptors Reduces Atherosclerotic Plaque Formation in Mice |
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