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Clearance of Fetuin-A–Containing Calciprotein Particles Is Mediated by Scavenger Receptor-A
RATIONALE:Fetuin-A is a liver-derived plasma protein involved in the regulation of calcified matrix metabolism. Biochemical studies showed that fetuin-A is essential for the formation of protein-mineral complexes, called calciprotein particles (CPPs). CPPs must be cleared from circulation to prevent...
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Published in: | Circulation research 2012-08, Vol.111 (5), p.575-584 |
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creator | Herrmann, Marietta Schäfer, Cora Heiss, Alexander Gräber, Steffen Kinkeldey, Anne Büscher, Andrea Schmitt, Martin M.N Bornemann, Jörg Nimmerjahn, Falk Herrmann, Martin Helming, Laura Gordon, Siamon Jahnen-Dechent, Willi |
description | RATIONALE:Fetuin-A is a liver-derived plasma protein involved in the regulation of calcified matrix metabolism. Biochemical studies showed that fetuin-A is essential for the formation of protein-mineral complexes, called calciprotein particles (CPPs). CPPs must be cleared from circulation to prevent local deposition and pathological calcification.
OBJECTIVE:We studied CPP clearance in mice and in cell culture to identify the tissues, cells, and receptors involved in the clearance.
METHODS AND RESULTS:In mice, fetuin-A–containing CPPs were rapidly cleared by the reticuloendothelial system, namely Kupffer cells of the liver and marginal zone macrophages of the spleen. Macrophages from scavenger receptor-AI/II (SR-A)-deficient mice cleared CPPs less efficiently than macrophages from wild-type mice, suggesting that SR-AI/II is involved in CPP binding and endocytosis. Accordingly, we found reduced clearance of CPPs in SR-A/MARCO–deficient mice.
CONCLUSIONS:We could demonstrate that fetuin-A–containing CPPs facilitate the clearance of mineral debris by macrophages via SR-A. Since the same receptor also contributes to the uptake of modified low-density lipoprotein particles in atherosclerosis, defective endocytosis of both types of particle may impinge on lipid as well as mineral debris clearance in calcifying atherosclerosis. |
doi_str_mv | 10.1161/CIRCRESAHA.111.261479 |
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OBJECTIVE:We studied CPP clearance in mice and in cell culture to identify the tissues, cells, and receptors involved in the clearance.
METHODS AND RESULTS:In mice, fetuin-A–containing CPPs were rapidly cleared by the reticuloendothelial system, namely Kupffer cells of the liver and marginal zone macrophages of the spleen. Macrophages from scavenger receptor-AI/II (SR-A)-deficient mice cleared CPPs less efficiently than macrophages from wild-type mice, suggesting that SR-AI/II is involved in CPP binding and endocytosis. Accordingly, we found reduced clearance of CPPs in SR-A/MARCO–deficient mice.
CONCLUSIONS:We could demonstrate that fetuin-A–containing CPPs facilitate the clearance of mineral debris by macrophages via SR-A. Since the same receptor also contributes to the uptake of modified low-density lipoprotein particles in atherosclerosis, defective endocytosis of both types of particle may impinge on lipid as well as mineral debris clearance in calcifying atherosclerosis.</description><identifier>ISSN: 0009-7330</identifier><identifier>EISSN: 1524-4571</identifier><identifier>DOI: 10.1161/CIRCRESAHA.111.261479</identifier><identifier>PMID: 22753077</identifier><identifier>CODEN: CIRUAL</identifier><language>eng</language><publisher>Hagerstown, MD: American Heart Association, Inc</publisher><subject>alpha-2-HS-Glycoprotein - genetics ; alpha-2-HS-Glycoprotein - metabolism ; alpha-2-HS-Glycoprotein - pharmacology ; Animals ; Apolipoproteins E - genetics ; Atherosclerosis (general aspects, experimental research) ; Atherosclerosis - metabolism ; Atherosclerosis - pathology ; Biological and medical sciences ; Blood and lymphatic vessels ; Calcification, Physiologic - physiology ; Calcinosis - metabolism ; Calcinosis - pathology ; Calcium - blood ; Calcium-Binding Proteins - metabolism ; Cardiology. Vascular system ; Carotid Arteries - cytology ; Cattle ; Cell Line ; Endocytosis - physiology ; Fundamental and applied biological sciences. Psychology ; Kupffer Cells - cytology ; Kupffer Cells - metabolism ; Lipoproteins, LDL - metabolism ; Macrophages - cytology ; Macrophages - metabolism ; Medical sciences ; Mice ; Mice, Inbred C57BL ; Mice, Knockout ; Mononuclear Phagocyte System - metabolism ; Phosphates - blood ; Receptors, Immunologic - genetics ; Receptors, Immunologic - metabolism ; Scavenger Receptors, Class A - genetics ; Scavenger Receptors, Class A - metabolism ; Spleen - cytology ; Vertebrates: cardiovascular system</subject><ispartof>Circulation research, 2012-08, Vol.111 (5), p.575-584</ispartof><rights>2012 American Heart Association, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5491-d2d3fff8ce319b0d66e8431196b5a3c04523c02f222f07beb8c26702c14aaa703</citedby><cites>FETCH-LOGICAL-c5491-d2d3fff8ce319b0d66e8431196b5a3c04523c02f222f07beb8c26702c14aaa703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26281159$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22753077$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Herrmann, Marietta</creatorcontrib><creatorcontrib>Schäfer, Cora</creatorcontrib><creatorcontrib>Heiss, Alexander</creatorcontrib><creatorcontrib>Gräber, Steffen</creatorcontrib><creatorcontrib>Kinkeldey, Anne</creatorcontrib><creatorcontrib>Büscher, Andrea</creatorcontrib><creatorcontrib>Schmitt, Martin M.N</creatorcontrib><creatorcontrib>Bornemann, Jörg</creatorcontrib><creatorcontrib>Nimmerjahn, Falk</creatorcontrib><creatorcontrib>Herrmann, Martin</creatorcontrib><creatorcontrib>Helming, Laura</creatorcontrib><creatorcontrib>Gordon, Siamon</creatorcontrib><creatorcontrib>Jahnen-Dechent, Willi</creatorcontrib><title>Clearance of Fetuin-A–Containing Calciprotein Particles Is Mediated by Scavenger Receptor-A</title><title>Circulation research</title><addtitle>Circ Res</addtitle><description>RATIONALE:Fetuin-A is a liver-derived plasma protein involved in the regulation of calcified matrix metabolism. Biochemical studies showed that fetuin-A is essential for the formation of protein-mineral complexes, called calciprotein particles (CPPs). CPPs must be cleared from circulation to prevent local deposition and pathological calcification.
OBJECTIVE:We studied CPP clearance in mice and in cell culture to identify the tissues, cells, and receptors involved in the clearance.
METHODS AND RESULTS:In mice, fetuin-A–containing CPPs were rapidly cleared by the reticuloendothelial system, namely Kupffer cells of the liver and marginal zone macrophages of the spleen. Macrophages from scavenger receptor-AI/II (SR-A)-deficient mice cleared CPPs less efficiently than macrophages from wild-type mice, suggesting that SR-AI/II is involved in CPP binding and endocytosis. Accordingly, we found reduced clearance of CPPs in SR-A/MARCO–deficient mice.
CONCLUSIONS:We could demonstrate that fetuin-A–containing CPPs facilitate the clearance of mineral debris by macrophages via SR-A. Since the same receptor also contributes to the uptake of modified low-density lipoprotein particles in atherosclerosis, defective endocytosis of both types of particle may impinge on lipid as well as mineral debris clearance in calcifying atherosclerosis.</description><subject>alpha-2-HS-Glycoprotein - genetics</subject><subject>alpha-2-HS-Glycoprotein - metabolism</subject><subject>alpha-2-HS-Glycoprotein - pharmacology</subject><subject>Animals</subject><subject>Apolipoproteins E - genetics</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Atherosclerosis - metabolism</subject><subject>Atherosclerosis - pathology</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Calcification, Physiologic - physiology</subject><subject>Calcinosis - metabolism</subject><subject>Calcinosis - pathology</subject><subject>Calcium - blood</subject><subject>Calcium-Binding Proteins - metabolism</subject><subject>Cardiology. Vascular system</subject><subject>Carotid Arteries - cytology</subject><subject>Cattle</subject><subject>Cell Line</subject><subject>Endocytosis - physiology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Kupffer Cells - cytology</subject><subject>Kupffer Cells - metabolism</subject><subject>Lipoproteins, LDL - metabolism</subject><subject>Macrophages - cytology</subject><subject>Macrophages - metabolism</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Knockout</subject><subject>Mononuclear Phagocyte System - metabolism</subject><subject>Phosphates - blood</subject><subject>Receptors, Immunologic - genetics</subject><subject>Receptors, Immunologic - metabolism</subject><subject>Scavenger Receptors, Class A - genetics</subject><subject>Scavenger Receptors, Class A - metabolism</subject><subject>Spleen - cytology</subject><subject>Vertebrates: cardiovascular system</subject><issn>0009-7330</issn><issn>1524-4571</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpFkcFu1DAQQC0EokvhE0C5IPWSMmM7cXKMopauVATawhFFjjNuDd5ksROq3vgH_pAvwatd6GVGY72Zsd4w9hrhHLHEd-16024ubpqrJtV4zkuUqn7CVlhwmctC4VO2AoA6V0LACXsR4zcAlILXz9kJ56oQoNSKfW096aBHQ9lks0uaFzfmzZ9fv9tpnLUb3XibtdobtwvTTG7MPukwO-MpZuuYfaDB6ZmGrH_Iboz-SeMthWxDhnbzFPLmJXtmtY_06phP2ZfLi8_tVX798f26ba5zU8ga84EPwlpbGRJY9zCUJVVSINZlX2hhQBY8RW455xZUT31leKmAG5RaawXilJ0d5qZf_lgozt3WRUPe65GmJXYIQhYoJIiEFgfUhCnGQLbbBbfV4SFB3d5s92g21dgdzKa-N8cVS7-l4X_XP5UJeHsEdDTa271UFx-5kleIxX6QPHD3k58pxO9-uafQ3ZH2812XTgYCkOc8BahQQZ5eEMVfAl6RfA</recordid><startdate>20120817</startdate><enddate>20120817</enddate><creator>Herrmann, Marietta</creator><creator>Schäfer, Cora</creator><creator>Heiss, Alexander</creator><creator>Gräber, Steffen</creator><creator>Kinkeldey, Anne</creator><creator>Büscher, Andrea</creator><creator>Schmitt, Martin M.N</creator><creator>Bornemann, Jörg</creator><creator>Nimmerjahn, Falk</creator><creator>Herrmann, Martin</creator><creator>Helming, Laura</creator><creator>Gordon, Siamon</creator><creator>Jahnen-Dechent, Willi</creator><general>American Heart Association, Inc</general><general>Lippincott Williams & Wilkins</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></search><sort><creationdate>20120817</creationdate><title>Clearance of Fetuin-A–Containing Calciprotein Particles Is Mediated by Scavenger Receptor-A</title><author>Herrmann, Marietta ; Schäfer, Cora ; Heiss, Alexander ; Gräber, Steffen ; Kinkeldey, Anne ; Büscher, Andrea ; Schmitt, Martin M.N ; Bornemann, Jörg ; Nimmerjahn, Falk ; Herrmann, Martin ; Helming, Laura ; Gordon, Siamon ; Jahnen-Dechent, Willi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5491-d2d3fff8ce319b0d66e8431196b5a3c04523c02f222f07beb8c26702c14aaa703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>alpha-2-HS-Glycoprotein - genetics</topic><topic>alpha-2-HS-Glycoprotein - metabolism</topic><topic>alpha-2-HS-Glycoprotein - pharmacology</topic><topic>Animals</topic><topic>Apolipoproteins E - genetics</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Atherosclerosis - metabolism</topic><topic>Atherosclerosis - pathology</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Calcification, Physiologic - physiology</topic><topic>Calcinosis - metabolism</topic><topic>Calcinosis - pathology</topic><topic>Calcium - blood</topic><topic>Calcium-Binding Proteins - metabolism</topic><topic>Cardiology. Vascular system</topic><topic>Carotid Arteries - cytology</topic><topic>Cattle</topic><topic>Cell Line</topic><topic>Endocytosis - physiology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Kupffer Cells - cytology</topic><topic>Kupffer Cells - metabolism</topic><topic>Lipoproteins, LDL - metabolism</topic><topic>Macrophages - cytology</topic><topic>Macrophages - metabolism</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Knockout</topic><topic>Mononuclear Phagocyte System - metabolism</topic><topic>Phosphates - blood</topic><topic>Receptors, Immunologic - genetics</topic><topic>Receptors, Immunologic - metabolism</topic><topic>Scavenger Receptors, Class A - genetics</topic><topic>Scavenger Receptors, Class A - metabolism</topic><topic>Spleen - cytology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Herrmann, Marietta</creatorcontrib><creatorcontrib>Schäfer, Cora</creatorcontrib><creatorcontrib>Heiss, Alexander</creatorcontrib><creatorcontrib>Gräber, Steffen</creatorcontrib><creatorcontrib>Kinkeldey, Anne</creatorcontrib><creatorcontrib>Büscher, Andrea</creatorcontrib><creatorcontrib>Schmitt, Martin M.N</creatorcontrib><creatorcontrib>Bornemann, Jörg</creatorcontrib><creatorcontrib>Nimmerjahn, Falk</creatorcontrib><creatorcontrib>Herrmann, Martin</creatorcontrib><creatorcontrib>Helming, Laura</creatorcontrib><creatorcontrib>Gordon, Siamon</creatorcontrib><creatorcontrib>Jahnen-Dechent, Willi</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><jtitle>Circulation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Herrmann, Marietta</au><au>Schäfer, Cora</au><au>Heiss, Alexander</au><au>Gräber, Steffen</au><au>Kinkeldey, Anne</au><au>Büscher, Andrea</au><au>Schmitt, Martin M.N</au><au>Bornemann, Jörg</au><au>Nimmerjahn, Falk</au><au>Herrmann, Martin</au><au>Helming, Laura</au><au>Gordon, Siamon</au><au>Jahnen-Dechent, Willi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clearance of Fetuin-A–Containing Calciprotein Particles Is Mediated by Scavenger Receptor-A</atitle><jtitle>Circulation research</jtitle><addtitle>Circ Res</addtitle><date>2012-08-17</date><risdate>2012</risdate><volume>111</volume><issue>5</issue><spage>575</spage><epage>584</epage><pages>575-584</pages><issn>0009-7330</issn><eissn>1524-4571</eissn><coden>CIRUAL</coden><abstract>RATIONALE:Fetuin-A is a liver-derived plasma protein involved in the regulation of calcified matrix metabolism. Biochemical studies showed that fetuin-A is essential for the formation of protein-mineral complexes, called calciprotein particles (CPPs). CPPs must be cleared from circulation to prevent local deposition and pathological calcification.
OBJECTIVE:We studied CPP clearance in mice and in cell culture to identify the tissues, cells, and receptors involved in the clearance.
METHODS AND RESULTS:In mice, fetuin-A–containing CPPs were rapidly cleared by the reticuloendothelial system, namely Kupffer cells of the liver and marginal zone macrophages of the spleen. Macrophages from scavenger receptor-AI/II (SR-A)-deficient mice cleared CPPs less efficiently than macrophages from wild-type mice, suggesting that SR-AI/II is involved in CPP binding and endocytosis. Accordingly, we found reduced clearance of CPPs in SR-A/MARCO–deficient mice.
CONCLUSIONS:We could demonstrate that fetuin-A–containing CPPs facilitate the clearance of mineral debris by macrophages via SR-A. Since the same receptor also contributes to the uptake of modified low-density lipoprotein particles in atherosclerosis, defective endocytosis of both types of particle may impinge on lipid as well as mineral debris clearance in calcifying atherosclerosis.</abstract><cop>Hagerstown, MD</cop><pub>American Heart Association, Inc</pub><pmid>22753077</pmid><doi>10.1161/CIRCRESAHA.111.261479</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | alpha-2-HS-Glycoprotein - genetics alpha-2-HS-Glycoprotein - metabolism alpha-2-HS-Glycoprotein - pharmacology Animals Apolipoproteins E - genetics Atherosclerosis (general aspects, experimental research) Atherosclerosis - metabolism Atherosclerosis - pathology Biological and medical sciences Blood and lymphatic vessels Calcification, Physiologic - physiology Calcinosis - metabolism Calcinosis - pathology Calcium - blood Calcium-Binding Proteins - metabolism Cardiology. Vascular system Carotid Arteries - cytology Cattle Cell Line Endocytosis - physiology Fundamental and applied biological sciences. Psychology Kupffer Cells - cytology Kupffer Cells - metabolism Lipoproteins, LDL - metabolism Macrophages - cytology Macrophages - metabolism Medical sciences Mice Mice, Inbred C57BL Mice, Knockout Mononuclear Phagocyte System - metabolism Phosphates - blood Receptors, Immunologic - genetics Receptors, Immunologic - metabolism Scavenger Receptors, Class A - genetics Scavenger Receptors, Class A - metabolism Spleen - cytology Vertebrates: cardiovascular system |
title | Clearance of Fetuin-A–Containing Calciprotein Particles Is Mediated by Scavenger Receptor-A |
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