8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.

Epoxyeicosatrienoic acids (EETs), synthesized from arachidonic acid by cytochrome P450 epoxygenases, are converted to dihydroxyeicosatrienoic acids by soluble epoxide hydrolase. EETs exert anti-inflammatory effects. However, the effect of EETs on humoral immunity is poorly understood. The present st...

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Main Authors: Yanxiang Gao, Juan Feng, Kongyang Ma, Zhou Zhou, Yi Zhu, Qingbo Xu, Xian Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3389024?pdf=render
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spelling doaj-2d00fb1b08f44a22b3a82e103dd2abfa2020-11-25T01:48:09ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0177e4025810.1371/journal.pone.00402588,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.Yanxiang GaoJuan FengKongyang MaZhou ZhouYi ZhuQingbo XuXian WangEpoxyeicosatrienoic acids (EETs), synthesized from arachidonic acid by cytochrome P450 epoxygenases, are converted to dihydroxyeicosatrienoic acids by soluble epoxide hydrolase. EETs exert anti-inflammatory effects. However, the effect of EETs on humoral immunity is poorly understood. The present study is to investigate the potential role of EETs on B cell function and mechanisms. We examined the role of EETs on antibody production of splenic B cells from C57BL/6 and apolipoprotein E-deficient (ApoE-/-) mice by means of ELISA. Of the 4 EET regioisomers, 8,9-EET decreased basal and activation-induced B cell antibody secretion. As well, 8,9-EET significantly inhibited B-cell proliferation and survival, plasma cell differentiation and class-switch recombination. Western blot analysis revealed that lipopolysaccharide-induced nuclear translocation of NF-κB could be attenuated by 8,9-EET. Furthermore, germinal center formation was impaired by 8,9-EET in mice in vivo. 8,9-EET may inhibit B-cell function in vitro and in vivo, which suggests a new therapeutic strategy for diseases with excess B cell activation.http://europepmc.org/articles/PMC3389024?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Yanxiang Gao
Juan Feng
Kongyang Ma
Zhou Zhou
Yi Zhu
Qingbo Xu
Xian Wang
spellingShingle Yanxiang Gao
Juan Feng
Kongyang Ma
Zhou Zhou
Yi Zhu
Qingbo Xu
Xian Wang
8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.
PLoS ONE
author_facet Yanxiang Gao
Juan Feng
Kongyang Ma
Zhou Zhou
Yi Zhu
Qingbo Xu
Xian Wang
author_sort Yanxiang Gao
title 8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.
title_short 8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.
title_full 8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.
title_fullStr 8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.
title_full_unstemmed 8,9-Epoxyeicosatrienoic acid inhibits antibody production of B lymphocytes in mice.
title_sort 8,9-epoxyeicosatrienoic acid inhibits antibody production of b lymphocytes in mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Epoxyeicosatrienoic acids (EETs), synthesized from arachidonic acid by cytochrome P450 epoxygenases, are converted to dihydroxyeicosatrienoic acids by soluble epoxide hydrolase. EETs exert anti-inflammatory effects. However, the effect of EETs on humoral immunity is poorly understood. The present study is to investigate the potential role of EETs on B cell function and mechanisms. We examined the role of EETs on antibody production of splenic B cells from C57BL/6 and apolipoprotein E-deficient (ApoE-/-) mice by means of ELISA. Of the 4 EET regioisomers, 8,9-EET decreased basal and activation-induced B cell antibody secretion. As well, 8,9-EET significantly inhibited B-cell proliferation and survival, plasma cell differentiation and class-switch recombination. Western blot analysis revealed that lipopolysaccharide-induced nuclear translocation of NF-κB could be attenuated by 8,9-EET. Furthermore, germinal center formation was impaired by 8,9-EET in mice in vivo. 8,9-EET may inhibit B-cell function in vitro and in vivo, which suggests a new therapeutic strategy for diseases with excess B cell activation.
url http://europepmc.org/articles/PMC3389024?pdf=render
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