Role of the soluble pattern recognition receptor PTX3 in vascular biology

•  Introduction •  PTX3 gene and expression •  PTX3 protein structure •  PTX3 ligands •  PTX3 in vascular pathology ‐  PTX3 as a marker of vascular damage ‐  Atherosclerosis ‐  Angiogenesis ‐  Restenosis •  Concluding remarks Pentraxins act as soluble pattern recognition receptors with a wide range...

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Veröffentlicht in:Journal of cellular and molecular medicine 2007-07, Vol.11 (4), p.723-738
Hauptverfasser: Presta, Marco, Camozzi, Maura, Salvatori, Giovanni, Rusnati, Marco
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Salvatori, Giovanni
Rusnati, Marco
description •  Introduction •  PTX3 gene and expression •  PTX3 protein structure •  PTX3 ligands •  PTX3 in vascular pathology ‐  PTX3 as a marker of vascular damage ‐  Atherosclerosis ‐  Angiogenesis ‐  Restenosis •  Concluding remarks Pentraxins act as soluble pattern recognition receptors with a wide range of functions in various pathophysiological conditions. The long‐pentraxin PTX3 shares the C‐terminal pentraxin‐domain with short‐pentraxins C‐reactive protein and serum amyloid P component and possesses an unique N‐terminal domain. These structural features suggest that PTX3 may have both overlapping and distinct biological/ligand recognition properties when compared to short‐pentraxins. PTX3 serves as a mechanism of amplification of inflammation and innate immunity. Indeed, vessel wall elements produce high amounts of PTX3 during inflammation and the levels of circulating PTX3 increase in several pathological conditions affecting the cardiovascular system. PTX3 exists as a free or extracellular matrix‐associated molecule and it binds the complement fraction C1q. PTX3 binds also apoptotic cells and selected pathogens, playing a role in innate immunity processes. In endothelial cells and macrophages, PTX3 upregulates tissue factor expression, suggesting its action as a regulator of endothelium during thrombogenesis and ischaemic vascular disease. Finally, PTX3 binds the angiogenic fibroblast growth factor‐2, thus inhibiting its biological activity. Taken together, these properties point to a role for PTX3 during vascular damage, angiogenesis, atherosclerosis, and restenosis.
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The long‐pentraxin PTX3 shares the C‐terminal pentraxin‐domain with short‐pentraxins C‐reactive protein and serum amyloid P component and possesses an unique N‐terminal domain. These structural features suggest that PTX3 may have both overlapping and distinct biological/ligand recognition properties when compared to short‐pentraxins. PTX3 serves as a mechanism of amplification of inflammation and innate immunity. Indeed, vessel wall elements produce high amounts of PTX3 during inflammation and the levels of circulating PTX3 increase in several pathological conditions affecting the cardiovascular system. PTX3 exists as a free or extracellular matrix‐associated molecule and it binds the complement fraction C1q. PTX3 binds also apoptotic cells and selected pathogens, playing a role in innate immunity processes. In endothelial cells and macrophages, PTX3 upregulates tissue factor expression, suggesting its action as a regulator of endothelium during thrombogenesis and ischaemic vascular disease. Finally, PTX3 binds the angiogenic fibroblast growth factor‐2, thus inhibiting its biological activity. 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The long‐pentraxin PTX3 shares the C‐terminal pentraxin‐domain with short‐pentraxins C‐reactive protein and serum amyloid P component and possesses an unique N‐terminal domain. These structural features suggest that PTX3 may have both overlapping and distinct biological/ligand recognition properties when compared to short‐pentraxins. PTX3 serves as a mechanism of amplification of inflammation and innate immunity. Indeed, vessel wall elements produce high amounts of PTX3 during inflammation and the levels of circulating PTX3 increase in several pathological conditions affecting the cardiovascular system. PTX3 exists as a free or extracellular matrix‐associated molecule and it binds the complement fraction C1q. PTX3 binds also apoptotic cells and selected pathogens, playing a role in innate immunity processes. In endothelial cells and macrophages, PTX3 upregulates tissue factor expression, suggesting its action as a regulator of endothelium during thrombogenesis and ischaemic vascular disease. Finally, PTX3 binds the angiogenic fibroblast growth factor‐2, thus inhibiting its biological activity. Taken together, these properties point to a role for PTX3 during vascular damage, angiogenesis, atherosclerosis, and restenosis.</description><subject>Adipocytes</subject><subject>Amino Acid Sequence</subject><subject>Amino acids</subject><subject>Amyloid P component</subject><subject>Angiogenesis</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Arteriosclerosis</subject><subject>atherosclerosis</subject><subject>bacteria</subject><subject>Biological activity</subject><subject>Blood Vessels - metabolism</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - chemistry</subject><subject>C-Reactive Protein - genetics</subject><subject>C-Reactive Protein - metabolism</subject><subject>Cardiovascular system</subject><subject>Cells</subject><subject>complement</subject><subject>Complement component C1q</subject><subject>Cytokines</subject><subject>Dendritic cells</subject><subject>Endothelial cells</subject><subject>Endothelium</subject><subject>Extracellular matrix</subject><subject>FGF</subject><subject>Fibroblast growth factor 2</subject><subject>Fibroblasts</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Innate immunity</subject><subject>Ischemia</subject><subject>Ligands</subject><subject>Macrophages</subject><subject>Molecular Sequence Data</subject><subject>Molecules</subject><subject>Nerve Tissue Proteins - chemistry</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Nervous system</subject><subject>Pathogens</subject><subject>Pattern recognition</subject><subject>Pattern recognition receptors</subject><subject>pentraxin</subject><subject>Pentraxins</subject><subject>Peptides</subject><subject>Protein structure</subject><subject>Proteins</subject><subject>Receptors, Pattern Recognition - metabolism</subject><subject>Restenosis</subject><subject>Reviews</subject><subject>Rheumatoid arthritis</subject><subject>Solubility</subject><subject>Tissue factor</subject><subject>Tissues</subject><subject>Vascular Diseases</subject><subject>vasculitis</subject><issn>1582-1838</issn><issn>1582-4934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqNkV9rFDEUxYMo9o9-BQkKfdsxN3cmyTwoyFK10qJIBd9CZiazzZKdrMlM7X77ZrtLtQXBvOSE-zuHXA4hFFgB-bxdFlApPitrLAvOmCwYYwKKmyfk8H7wdK9BoTogRyktGUMBWD8nByClYAqrQ3L2PXhLQ0_HK0tT8FOTn2szjjYONNo2LAY3unCn7XoMkX67_InUDfTapHbyJtLGBR8WmxfkWW98si_39zH58fH0cv55dv7109n8w_msrWqEWcdraBl2ouksx1aYvjGVVLySBhvWWAQlBfCadQ3n0koLXV_3HUJZWd5l5zF5v8tdT83Kdq0dxmi8Xke3MnGjg3H64WRwV3oRrjUqjrziOeBkHxDDr8mmUa9caq33ZrBhSloozkFVmME3j8BlmOKQl9PIZClRCiwz9fpfFAcJqoZaZEjtoDaGlKLt7_8LTG8r1Uu9bUtvm9PbSvVdpfomW1_9ve8f477DDLzbAb-dt5v_DtZf5hcXWeEt8LivVA</recordid><startdate>200707</startdate><enddate>200707</enddate><creator>Presta, Marco</creator><creator>Camozzi, Maura</creator><creator>Salvatori, Giovanni</creator><creator>Rusnati, Marco</creator><general>Blackwell Publishing Ltd</general><general>John Wiley &amp; 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The long‐pentraxin PTX3 shares the C‐terminal pentraxin‐domain with short‐pentraxins C‐reactive protein and serum amyloid P component and possesses an unique N‐terminal domain. These structural features suggest that PTX3 may have both overlapping and distinct biological/ligand recognition properties when compared to short‐pentraxins. PTX3 serves as a mechanism of amplification of inflammation and innate immunity. Indeed, vessel wall elements produce high amounts of PTX3 during inflammation and the levels of circulating PTX3 increase in several pathological conditions affecting the cardiovascular system. PTX3 exists as a free or extracellular matrix‐associated molecule and it binds the complement fraction C1q. PTX3 binds also apoptotic cells and selected pathogens, playing a role in innate immunity processes. In endothelial cells and macrophages, PTX3 upregulates tissue factor expression, suggesting its action as a regulator of endothelium during thrombogenesis and ischaemic vascular disease. Finally, PTX3 binds the angiogenic fibroblast growth factor‐2, thus inhibiting its biological activity. Taken together, these properties point to a role for PTX3 during vascular damage, angiogenesis, atherosclerosis, and restenosis.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17760835</pmid><doi>10.1111/j.1582-4934.2007.00061.x</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record>
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source Wiley Online Library Open Access
subjects Adipocytes
Amino Acid Sequence
Amino acids
Amyloid P component
Angiogenesis
Animals
Apoptosis
Arteriosclerosis
atherosclerosis
bacteria
Biological activity
Blood Vessels - metabolism
C-reactive protein
C-Reactive Protein - chemistry
C-Reactive Protein - genetics
C-Reactive Protein - metabolism
Cardiovascular system
Cells
complement
Complement component C1q
Cytokines
Dendritic cells
Endothelial cells
Endothelium
Extracellular matrix
FGF
Fibroblast growth factor 2
Fibroblasts
Gene expression
Humans
Inflammation
Innate immunity
Ischemia
Ligands
Macrophages
Molecular Sequence Data
Molecules
Nerve Tissue Proteins - chemistry
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - metabolism
Nervous system
Pathogens
Pattern recognition
Pattern recognition receptors
pentraxin
Pentraxins
Peptides
Protein structure
Proteins
Receptors, Pattern Recognition - metabolism
Restenosis
Reviews
Rheumatoid arthritis
Solubility
Tissue factor
Tissues
Vascular Diseases
vasculitis
title Role of the soluble pattern recognition receptor PTX3 in vascular biology
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