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Estrogen, NFkappaB, and the heat shock response.雌激素、核因子κB与热休克反应。
Mol Med. 2008 Jul-Aug;14(7-8):517-27. doi: 10.2119/2008-00026.Stice.
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Mitogen activated protein kinase (MAPK) mediates non-genomic pathway of estrogen on T cell cytokine production following trauma-hemorrhage.丝裂原活化蛋白激酶(MAPK)介导雌激素在创伤性出血后T细胞细胞因子产生方面的非基因组途径。
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Estrogen and CD4+ T cells.雌激素与CD4+ T细胞。
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The complex role of estrogens in inflammation.雌激素在炎症中的复杂作用。
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Systemic lupus erythematosus and hormone replacement therapy.系统性红斑狼疮与激素替代疗法。
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Effects of estrogen receptor subtype-selective agonists on autoimmune disease in lupus-prone NZB/NZW F1 mouse model.雌激素受体亚型选择性激动剂对狼疮易感NZB/NZW F1小鼠模型自身免疫性疾病的影响。
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Phosphoinositide-3-kinase/akt survival signal pathways are implicated in neuronal survival after stroke.磷酸肌醇-3-激酶/蛋白激酶B生存信号通路与中风后神经元的存活有关。
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Physiologically high concentrations of 17beta-estradiol enhance NF-kappaB activity in human T cells.生理浓度的17β-雌二醇可增强人T细胞中的核因子κB活性。
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雌激素增强 T 细胞依赖性免疫反应,但不增强 T 细胞非依赖性免疫反应。

Estrogen augments the T cell-dependent but not the T-independent immune response.

机构信息

Department of Immunology, Eötvös Loránd University, Budapest, Hungary.

出版信息

Cell Mol Life Sci. 2010 May;67(10):1661-74. doi: 10.1007/s00018-010-0270-5. Epub 2010 Feb 7.

DOI:10.1007/s00018-010-0270-5
PMID:20140748
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11115714/
Abstract

Estrogen plays a critical regulatory role in the development and maintenance of immunity. Its role in the regulation of antibody synthesis in vivo is still not completely clear. Here, we have compared the effect of estrogen on T cell-dependent (TD) and T cell-independent type 2 (TI-2) antibody responses. The results provide the first evidence that estrogen enhances the TD but not the TI-2 response. Ovariectomy significantly decreased, while estrogen re-administration increased the number of hapten-specific IgM- and IgG-producing cells in response to TD antigen. In vitro experiments also show that estrogen may have a direct impact on B and T cells by inducing rapid signaling events, such as Erk and AKT phosphorylation, cell-specific Ca(2+) signal, and NFkappaB activation. These non-transcriptional effects are mediated by classical estrogen receptors and partly by an as yet unidentified plasma membrane estrogen receptor. Such receptor- mediated rapid signals may modulate the in vivo T cell-dependent immune response.

摘要

雌激素在免疫的发育和维持中起着关键的调节作用。其在体内调节抗体合成中的作用尚不完全清楚。在这里,我们比较了雌激素对 T 细胞依赖性(TD)和 T 细胞非依赖性 2 型(TI-2)抗体应答的影响。结果首次提供了证据表明,雌激素增强了 TD 反应,但不增强 TI-2 反应。卵巢切除显著降低了 TD 抗原反应中半抗原特异性 IgM 和 IgG 产生细胞的数量,而雌激素再给药则增加了这些细胞的数量。体外实验还表明,雌激素可能通过诱导快速信号事件,如 Erk 和 AKT 磷酸化、细胞特异性 Ca(2+)信号和 NFkappaB 激活,对 B 和 T 细胞产生直接影响。这些非转录效应是通过经典的雌激素受体和部分尚未确定的质膜雌激素受体介导的。这种受体介导的快速信号可能调节体内 T 细胞依赖性免疫反应。