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Thymocyte Differentiation is Regulated by a Change in Estradiol Levels during the Estrous Cycle in Mouse

机译:胸腺细胞分化受小鼠发情周期中雌二醇水平变化的调节

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摘要

Recent study showed that T cells in the immune organs and peripheral blood are influenced by estradiol, leading to a dysfunction of the immune system. However, little is known about the thymic-gonadal relationship during the estrous cycle in mouse. Therefore, the purpose of this study was to elucidate the mechanism by which a change in estradiol levels during the estrous cycle regulates the development of T cells in the mouse thymus. Six-week-old ICR mice were used and divided into four groups, including diestrous, proestrous, estrous, and metestrous. We first confirmed that ER-α and - β estrogen receptors were expressed in thymic epithelial cells, showing that their expression was not different during the estrous cycle. There was also no significant difference in thymic weight and total number of thymocytes during the estrous cycle. To determine the degree of thymocyte differentiation during the estrous cycle, we analyzed thymocytes by flow cytometry. As a result, the percentage of CD4+CD8+ double-positive (DP) T cells was significantly decreased in the proestrous phase compared to the diestrous phase. However, CD4+CD8- or CD4-CD8+ (SP) T cells were significantly increased in the proestrous phase compared to the diestrous phase. In addition, the percentage of CD44+CD25- (DN1) T cells was significantly decreased in the estrous phase compared to other phases, whereas the percentages of CD44+CD25+ (DN2), CD44-CD25+ (DN3), and CD44-CD25- (DN4) were not changed during the estrous cycle. These results indicate that the development of thymocytes may arrest in the DP to SP transition stage in the proestrous phase displaying the highest serum level of estradiol. This study suggests that a change in estradiol levels during the estrous cycle may be involved in the regulation of thymocyte differentiation in the mouse thymus.
机译:最近的研究表明,雌二醇会影响免疫器官和外周血中的T细胞,从而导致免疫系统功能异常。然而,关于小鼠发情周期中胸腺-性腺关系的了解甚少。因此,本研究的目的是阐明发情周期中雌二醇水平变化调节小鼠胸腺T细胞发育的机制。使用六周龄的ICR小鼠,将其分为四组,分别是发情的,发情的,发情的和肠胃的。我们首先证实,ER-α和-β雌激素受体在胸腺上皮细胞中表达,表明它们在发情周期中的表达没有差异。在发情周期中胸腺重量和胸腺细胞总数也没有显着差异。为了确定发情周期中胸腺细胞的分化程度,我们通过流式细胞仪分析了胸腺细胞。结果,与发情期相比,在发情期CD4 + CD8 +双阳性(DP)T细胞的百分比显着降低。然而,与发情期相比,在发情期CD4 + CD8-或CD4-CD8 +(SP)T细胞显着增加。此外,与其他阶段相比,在发情期CD44 + CD25-(DN1)T细胞的百分比显着降低,而CD44 + CD25 +(DN2),CD44-CD25 +(DN3)和CD44-CD25- (DN4)在发情周期中未更改。这些结果表明胸腺细胞的发育可能在发情期的DP至SP过渡阶段停滞,显示出最高的雌二醇血清水平。这项研究表明,在发情周期中雌二醇水平的变化可能与小鼠胸腺中胸腺细胞分化的调节有关。

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