Department of Immunology, Eötvös Loránd University, Budapest, Hungary.
Cell Mol Life Sci. 2010 May;67(10):1661-74. doi: 10.1007/s00018-010-0270-5. Epub 2010 Feb 7.
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.
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。