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8,9-环氧二十碳三烯酸抑制小鼠 B 淋巴细胞抗体的产生。

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

机构信息

Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, People's Republic of China.

出版信息

PLoS One. 2012;7(7):e40258. doi: 10.1371/journal.pone.0040258. Epub 2012 Jul 3.

Abstract

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.

摘要

环氧二十碳三烯酸(EETs)是由细胞色素 P450 加氧酶从花生四烯酸合成的,可被可溶性环氧化物水解酶转化为二羟二十碳三烯酸。EETs 具有抗炎作用。然而,EETs 对体液免疫的影响尚不清楚。本研究旨在探讨 EETs 对 B 细胞功能和机制的潜在作用。我们通过 ELISA 检查了 EETs 对 C57BL/6 和载脂蛋白 E 缺陷(ApoE-/-)小鼠脾 B 细胞抗体产生的作用。在 4 种 EET 同分异构体中,8,9-EET 降低了基础和激活诱导的 B 细胞抗体分泌。此外,8,9-EET 还显著抑制了 B 细胞的增殖和存活、浆细胞分化和类别转换重组。Western blot 分析表明,8,9-EET 可减弱脂多糖诱导的 NF-κB 核转位。此外,8,9-EET 在体内还可损害生发中心的形成。8,9-EET 可能在体外和体内抑制 B 细胞功能,这为治疗过度 B 细胞激活的疾病提供了一种新的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae3f/3389024/822a7dfef6ed/pone.0040258.g002.jpg

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