Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.

<h4>Background</h4>The oxidation of proteins by endogenously generated free radicals causes structural modifications in the molecules that lead to generation of neo-antigenic epitopes that have implications in various autoimmune disorders, including rheumatoid arthritis (RA). Collagen in...

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Autores principales: Uzma Shahab, Saheem Ahmad, Moinuddin, Kiran Dixit, Safia Habib, Khursheed Alam, Asif Ali
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Publicado: Public Library of Science (PLoS) 2012
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spelling oai:doaj.org-article:5ddd0c5ffb3c4c1abaefd8f4d17d50a32021-11-18T07:28:52ZHydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.1932-620310.1371/journal.pone.0031199https://doaj.org/article/5ddd0c5ffb3c4c1abaefd8f4d17d50a32012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22319617/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>The oxidation of proteins by endogenously generated free radicals causes structural modifications in the molecules that lead to generation of neo-antigenic epitopes that have implications in various autoimmune disorders, including rheumatoid arthritis (RA). Collagen induced arthritis (CIA) in rodents (rats and mice) is an accepted experimental model for RA.<h4>Methodology/principal findings</h4>Hydroxyl radicals were generated by the Fenton reaction. Collagen type II (CII) was modified by •OH radical (CII-OH) and analysed by ultraviolet-visible (UV-VIS), fluorescence and circular dichroism (CD) spectroscopy. The immunogenicity of native and modified CII was checked in female Lewis rats and specificity of the induced antibodies was ascertained by enzyme linked immunosorbent assay (ELISA). The extent of CIA was evaluated by visual inspection. We also estimated the oxidative and inflammatory markers in the sera of immunized rats. A slight change in the triple helical structure of CII as well as fragmentation was observed after hydroxyl radical modification. The modified CII was found to be highly arthritogenic and immunogenic as compared to the native form. The CII-OH immunized rats exhibited increased oxidative stress and inflammation as compared to the CII immunized rats in the control group.<h4>Conclusions/significance</h4>Neo-antigenic epitopes were generated on (•)OH modified CII which rendered it highly immunogenic and arthritogenic as compared to the unmodified form. Since the rodent CIA model shares many features with human RA, these results illuminate the role of free radicals in human RA.Uzma ShahabSaheem AhmadMoinuddinKiran DixitSafia HabibKhursheed AlamAsif AliPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 2, p e31199 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Uzma Shahab
Saheem Ahmad
Moinuddin
Kiran Dixit
Safia Habib
Khursheed Alam
Asif Ali
Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.
description <h4>Background</h4>The oxidation of proteins by endogenously generated free radicals causes structural modifications in the molecules that lead to generation of neo-antigenic epitopes that have implications in various autoimmune disorders, including rheumatoid arthritis (RA). Collagen induced arthritis (CIA) in rodents (rats and mice) is an accepted experimental model for RA.<h4>Methodology/principal findings</h4>Hydroxyl radicals were generated by the Fenton reaction. Collagen type II (CII) was modified by •OH radical (CII-OH) and analysed by ultraviolet-visible (UV-VIS), fluorescence and circular dichroism (CD) spectroscopy. The immunogenicity of native and modified CII was checked in female Lewis rats and specificity of the induced antibodies was ascertained by enzyme linked immunosorbent assay (ELISA). The extent of CIA was evaluated by visual inspection. We also estimated the oxidative and inflammatory markers in the sera of immunized rats. A slight change in the triple helical structure of CII as well as fragmentation was observed after hydroxyl radical modification. The modified CII was found to be highly arthritogenic and immunogenic as compared to the native form. The CII-OH immunized rats exhibited increased oxidative stress and inflammation as compared to the CII immunized rats in the control group.<h4>Conclusions/significance</h4>Neo-antigenic epitopes were generated on (•)OH modified CII which rendered it highly immunogenic and arthritogenic as compared to the unmodified form. Since the rodent CIA model shares many features with human RA, these results illuminate the role of free radicals in human RA.
format article
author Uzma Shahab
Saheem Ahmad
Moinuddin
Kiran Dixit
Safia Habib
Khursheed Alam
Asif Ali
author_facet Uzma Shahab
Saheem Ahmad
Moinuddin
Kiran Dixit
Safia Habib
Khursheed Alam
Asif Ali
author_sort Uzma Shahab
title Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.
title_short Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.
title_full Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.
title_fullStr Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.
title_full_unstemmed Hydroxyl radical modification of collagen type II increases its arthritogenicity and immunogenicity.
title_sort hydroxyl radical modification of collagen type ii increases its arthritogenicity and immunogenicity.
publisher Public Library of Science (PLoS)
publishDate 2012
url https://doaj.org/article/5ddd0c5ffb3c4c1abaefd8f4d17d50a3
work_keys_str_mv AT uzmashahab hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
AT saheemahmad hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
AT moinuddin hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
AT kirandixit hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
AT safiahabib hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
AT khursheedalam hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
AT asifali hydroxylradicalmodificationofcollagentypeiiincreasesitsarthritogenicityandimmunogenicity
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