Relative efficiencies of peptidylarginine deiminase 2 and 4 in generating target sites for anti-citrullinated protein antibodies in fibrinogen, alpha-enolase and histone H3
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
K08 AR065500
NIAMS NIH HHS - United States
PubMed
30161253
PubMed Central
PMC6117052
DOI
10.1371/journal.pone.0203214
PII: PONE-D-18-05468
Knihovny.cz E-zdroje
- MeSH
- citrulinace MeSH
- fibrinogen imunologie MeSH
- fosfopyruváthydratasa imunologie MeSH
- histony imunologie MeSH
- koncentrace vodíkových iontů MeSH
- lidé MeSH
- peptidylarginindeiminasa typu 2 MeSH
- peptidylarginindeiminasa typu 4 MeSH
- peptidylarginindeiminasy metabolismus MeSH
- protilátky proti citrulinovaným peptidům metabolismus MeSH
- rekombinantní proteiny metabolismus MeSH
- revmatoidní artritida enzymologie imunologie MeSH
- sérový albumin imunologie MeSH
- synoviální tekutina MeSH
- techniky in vitro MeSH
- vápník metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Názvy látek
- fibrinogen MeSH
- fosfopyruváthydratasa MeSH
- histony MeSH
- PADI2 protein, human MeSH Prohlížeč
- PADI4 protein, human MeSH Prohlížeč
- peptidylarginindeiminasa typu 2 MeSH
- peptidylarginindeiminasa typu 4 MeSH
- peptidylarginindeiminasy MeSH
- protilátky proti citrulinovaným peptidům MeSH
- rekombinantní proteiny MeSH
- sérový albumin MeSH
- vápník MeSH
OBJECTIVE: Peptidylarginine deiminase 2 (PAD2) and PAD4 are expressed in the synovium of rheumatoid arthritis (RA) patients and catalyze citrullination of arginine residues in proteins targeted by anti-citrullinated protein antibodies (ACPAs). Little is known about the relative importance of PAD2 and PAD4 in generating citrullinated self-antigens. Here we investigate the ability of PAD2 and PAD4 to generate citrullinated targets for ACPAs in four human proteins. METHODS: Synovial fluid (SF) and plasma were collected from 42 RA patients. Human fibrinogen, human alpha-enolase (ENO1), human histone H3, and human serum albumin (HSA) were citrullinated in vitro by PAD2 or PAD4. The total degree of citrullination was determined using the anti-modified citrulline approach. Antibody binding to native and citrullinated proteins was measured by ELISA. RESULTS: ACPAs within pooled SF from multiple RA patients reacted equally well with, and cross-reacted with, PAD2- and PAD4-citrullinated fibrinogen. ACPAs from most individual patient SF and plasma samples bound equally well to PAD2- and PAD4-citrullinated fibrinogen or ENO1. When histone H3 was used as target, PAD4 was generally superior in generating epitopes recognized by ACPAs. No binding to citrullinated HSA was observed. CONCLUSION: In most patients, PAD2 and PAD4 are equally efficient in generating citrullinated target sites for ACPAs in fibrinogen and ENO1. The binding of autoantibodies to histone H3 was generally higher after citrullination with PAD4 than with PAD2. Citrullinated HSA is not a target for ACPAs.
Department of Health Science and Technology Aalborg University Aalborg Denmark
Department of Medicine University of Wisconsin Madison Wisconsin United States of America
William S Middleton Memorial Veterans Hospital Madison Wisconsin United States of America
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