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Synovial detection and autoantibody reactivity of processed citrullinated isoforms of vimentin in inflammatory arthritides

Objectives. To investigate the presence and characteristics of citrullinated vimentin in protein extracts of inflamed synovial tissue. Methods. Cytosolic protein extracts obtained from RA (n = 14) and SpA patients (n = 14) were analysed by gel electrophoresis and western blotting. Citrullinated vime...

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Published in:Rheumatology (Oxford, England) England), 2008-05, Vol.47 (5), p.597-604
Main Authors: Tilleman, K., Van Steendam, K., Cantaert, T., De Keyser, F., Elewaut, D., Deforce, D.
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cited_by cdi_FETCH-LOGICAL-c579t-e7bce8e384d21a7b4bb85085ca93c1ad879a014f787a80f74937b7388ea48b8b3
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container_title Rheumatology (Oxford, England)
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creator Tilleman, K.
Van Steendam, K.
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Elewaut, D.
Deforce, D.
description Objectives. To investigate the presence and characteristics of citrullinated vimentin in protein extracts of inflamed synovial tissue. Methods. Cytosolic protein extracts obtained from RA (n = 14) and SpA patients (n = 14) were analysed by gel electrophoresis and western blotting. Citrullinated vimentin isoforms were visualized by a combination of anti-modified citrulline (AMC) staining and anti-vimentin detections (V9, H-84). This was subsequently confirmed by immunoprecipitation. Autoantibody detection was verified using sera obtained form RA (n = 6) and SpA (n = 6) patients. Results. A specific cluster of spots displayed on the 2D gel images of cytosolic synovial tissue extracts, was identified by mass spectrometry as vimentin. Interestingly, our results suggested that these isoforms could be the result of caspase cleavage. In addition, these cleaved forms of vimentin were found to be citrullinated in synovial cytosolic protein extracts of inflammatory arthritides, mainly in RA patients. Caspase-3 is able to cleave vimentin at amino acid 85. Western blot analysis with a specific antibody against amino acids 1–84 of vimentin (H-84) confirmed that the citrullinated isoforms of vimentin were lacking this part of the protein. These results were also confirmed by immunoprecipitation of vimentin derived from cytosolic protein extracts of RA and SpA patients. Furthermore, the presence of autoantibodies against these citrullinated processed forms of vimentin was found to be predominantly associated with RA patients. Conclusions. These findings show the presence of processed citrullinated vimentin in inflammatory arthritides, mainly in RA and suggest a possible origin of the ACPA immune response in RA.
doi_str_mv 10.1093/rheumatology/ken077
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To investigate the presence and characteristics of citrullinated vimentin in protein extracts of inflamed synovial tissue. Methods. Cytosolic protein extracts obtained from RA (n = 14) and SpA patients (n = 14) were analysed by gel electrophoresis and western blotting. Citrullinated vimentin isoforms were visualized by a combination of anti-modified citrulline (AMC) staining and anti-vimentin detections (V9, H-84). This was subsequently confirmed by immunoprecipitation. Autoantibody detection was verified using sera obtained form RA (n = 6) and SpA (n = 6) patients. Results. A specific cluster of spots displayed on the 2D gel images of cytosolic synovial tissue extracts, was identified by mass spectrometry as vimentin. Interestingly, our results suggested that these isoforms could be the result of caspase cleavage. In addition, these cleaved forms of vimentin were found to be citrullinated in synovial cytosolic protein extracts of inflammatory arthritides, mainly in RA patients. Caspase-3 is able to cleave vimentin at amino acid 85. Western blot analysis with a specific antibody against amino acids 1–84 of vimentin (H-84) confirmed that the citrullinated isoforms of vimentin were lacking this part of the protein. These results were also confirmed by immunoprecipitation of vimentin derived from cytosolic protein extracts of RA and SpA patients. Furthermore, the presence of autoantibodies against these citrullinated processed forms of vimentin was found to be predominantly associated with RA patients. Conclusions. These findings show the presence of processed citrullinated vimentin in inflammatory arthritides, mainly in RA and suggest a possible origin of the ACPA immune response in RA.</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/ken077</identifier><identifier>PMID: 18326534</identifier><identifier>CODEN: BJRHDF</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Aged ; Antigen-Antibody Reactions ; Arthritis - immunology ; Arthritis, Rheumatoid - immunology ; Autoantibodies ; Autoantibodies - blood ; Autoantibodies - immunology ; Autoantigens - immunology ; Biological and medical sciences ; Blotting, Western - methods ; Caspase 3 - metabolism ; Citrullinated vimentin ; Citrulline - metabolism ; Diseases of the osteoarticular system ; Electrophoresis, Polyacrylamide Gel ; Female ; Human ; Humans ; Immunoprecipitation ; Inflammation ; Inflammatory joint diseases ; Male ; Medical sciences ; Middle Aged ; Protein Isoforms - analysis ; Protein Isoforms - immunology ; Rheumatoid arthritis ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Spondylitis, Ankylosing - immunology ; Synovial Membrane - chemistry ; Synovial Membrane - immunology ; Vimentin - analysis ; Vimentin - immunology ; Vimentin - metabolism</subject><ispartof>Rheumatology (Oxford, England), 2008-05, Vol.47 (5), p.597-604</ispartof><rights>2008 The Author(s) 2008</rights><rights>2008 INIST-CNRS</rights><rights>2008 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c579t-e7bce8e384d21a7b4bb85085ca93c1ad879a014f787a80f74937b7388ea48b8b3</citedby><cites>FETCH-LOGICAL-c579t-e7bce8e384d21a7b4bb85085ca93c1ad879a014f787a80f74937b7388ea48b8b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20282721$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18326534$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tilleman, K.</creatorcontrib><creatorcontrib>Van Steendam, K.</creatorcontrib><creatorcontrib>Cantaert, T.</creatorcontrib><creatorcontrib>De Keyser, F.</creatorcontrib><creatorcontrib>Elewaut, D.</creatorcontrib><creatorcontrib>Deforce, D.</creatorcontrib><title>Synovial detection and autoantibody reactivity of processed citrullinated isoforms of vimentin in inflammatory arthritides</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>Objectives. To investigate the presence and characteristics of citrullinated vimentin in protein extracts of inflamed synovial tissue. Methods. Cytosolic protein extracts obtained from RA (n = 14) and SpA patients (n = 14) were analysed by gel electrophoresis and western blotting. Citrullinated vimentin isoforms were visualized by a combination of anti-modified citrulline (AMC) staining and anti-vimentin detections (V9, H-84). This was subsequently confirmed by immunoprecipitation. Autoantibody detection was verified using sera obtained form RA (n = 6) and SpA (n = 6) patients. Results. A specific cluster of spots displayed on the 2D gel images of cytosolic synovial tissue extracts, was identified by mass spectrometry as vimentin. Interestingly, our results suggested that these isoforms could be the result of caspase cleavage. In addition, these cleaved forms of vimentin were found to be citrullinated in synovial cytosolic protein extracts of inflammatory arthritides, mainly in RA patients. Caspase-3 is able to cleave vimentin at amino acid 85. Western blot analysis with a specific antibody against amino acids 1–84 of vimentin (H-84) confirmed that the citrullinated isoforms of vimentin were lacking this part of the protein. These results were also confirmed by immunoprecipitation of vimentin derived from cytosolic protein extracts of RA and SpA patients. Furthermore, the presence of autoantibodies against these citrullinated processed forms of vimentin was found to be predominantly associated with RA patients. Conclusions. 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To investigate the presence and characteristics of citrullinated vimentin in protein extracts of inflamed synovial tissue. Methods. Cytosolic protein extracts obtained from RA (n = 14) and SpA patients (n = 14) were analysed by gel electrophoresis and western blotting. Citrullinated vimentin isoforms were visualized by a combination of anti-modified citrulline (AMC) staining and anti-vimentin detections (V9, H-84). This was subsequently confirmed by immunoprecipitation. Autoantibody detection was verified using sera obtained form RA (n = 6) and SpA (n = 6) patients. Results. A specific cluster of spots displayed on the 2D gel images of cytosolic synovial tissue extracts, was identified by mass spectrometry as vimentin. Interestingly, our results suggested that these isoforms could be the result of caspase cleavage. In addition, these cleaved forms of vimentin were found to be citrullinated in synovial cytosolic protein extracts of inflammatory arthritides, mainly in RA patients. Caspase-3 is able to cleave vimentin at amino acid 85. Western blot analysis with a specific antibody against amino acids 1–84 of vimentin (H-84) confirmed that the citrullinated isoforms of vimentin were lacking this part of the protein. These results were also confirmed by immunoprecipitation of vimentin derived from cytosolic protein extracts of RA and SpA patients. Furthermore, the presence of autoantibodies against these citrullinated processed forms of vimentin was found to be predominantly associated with RA patients. Conclusions. These findings show the presence of processed citrullinated vimentin in inflammatory arthritides, mainly in RA and suggest a possible origin of the ACPA immune response in RA.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>18326534</pmid><doi>10.1093/rheumatology/ken077</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Antigen-Antibody Reactions
Arthritis - immunology
Arthritis, Rheumatoid - immunology
Autoantibodies
Autoantibodies - blood
Autoantibodies - immunology
Autoantigens - immunology
Biological and medical sciences
Blotting, Western - methods
Caspase 3 - metabolism
Citrullinated vimentin
Citrulline - metabolism
Diseases of the osteoarticular system
Electrophoresis, Polyacrylamide Gel
Female
Human
Humans
Immunoprecipitation
Inflammation
Inflammatory joint diseases
Male
Medical sciences
Middle Aged
Protein Isoforms - analysis
Protein Isoforms - immunology
Rheumatoid arthritis
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Spondylitis, Ankylosing - immunology
Synovial Membrane - chemistry
Synovial Membrane - immunology
Vimentin - analysis
Vimentin - immunology
Vimentin - metabolism
title Synovial detection and autoantibody reactivity of processed citrullinated isoforms of vimentin in inflammatory arthritides
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