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基于淋巴细胞基因表达谱揭示淫羊藿黄酮对衰老大鼠免疫稳态重塑的分子机制

[Molecular mechanism of epimedium flavonoids in immune homeostasis remodeling in aged rats revealed by lymphocyte gene expression profile].

作者信息

Chen Yu, Shen Zi-yin, Chen Wei-hua

机构信息

Institute of Integrative Chinese and Western Medicine, Huashan Hospital, Fudan University, Shanghai 200040.

出版信息

Zhongguo Zhong Xi Yi Jie He Za Zhi. 2004 Jan;24(1):59-62.

Abstract

OBJECTIVE

To elucidate the gene regulatory pattern of Epimedium flavonoids (EF) in immune homeostasis remodeling in the aged rats.

METHODS

(1) To quantitatively analyse the apoptosis percentage of lymphocyte in spleen of aged, young and EF treated rats using flow cytometry. (2) To analyse the lymphocyte gene expression profiles of different groups using gene chips (Rat Genome U34A).

RESULTS

(1) Detection of lymphocyte apoptosis percentage showed that there was significant difference in comparing between aged group and young group, between EF treated group and aged group (P < 0.01). (2) As compared with that in the young group, in the aged group, 116 genes were up-regulated and 215 down-regulated. As compared with that in the old group, in the EF treated group, 447 genes were up-regulated and 456 down-regulated, which involved the aspects as cell apoptosis and cell proliferation regulation, etc.

CONCLUSION

(1) The expression pattern characterized by up-regulation of apoptosis promoting genes expression and down-regulation of apoptosis inhibiting genes expression, is the important gene background of immuno-homeostasis imbalance in the aged. (2) The role of EF is to reverse the abnormal changes of gene expressions with opposite functions, i.e. the apoptosis promoting and inhibiting, proliferation enhancing and antagonizing genes, to reconstruct a beneficial equilibrium of gene expression and thus to further remodel the immuno-homeostasis in the aged.

摘要

目的

阐明淫羊藿黄酮(EF)在老年大鼠免疫稳态重塑中的基因调控模式。

方法

(1)采用流式细胞术定量分析老年、青年及EF处理大鼠脾脏淋巴细胞凋亡率。(2)使用基因芯片(大鼠基因组U34A)分析不同组别的淋巴细胞基因表达谱。

结果

(1)淋巴细胞凋亡率检测显示,老年组与青年组、EF处理组与老年组比较差异有统计学意义(P<0.01)。(2)与青年组相比,老年组上调基因116个,下调基因215个。与老年组相比,EF处理组上调基因447个,下调基因456个,涉及细胞凋亡、细胞增殖调控等方面。

结论

(1)以促凋亡基因表达上调、抑凋亡基因表达下调为特征的表达模式是老年免疫稳态失衡的重要基因背景。(2)EF的作用是逆转促凋亡与抑凋亡、促增殖与抗增殖等功能相反的基因表达异常变化,重建有益的基因表达平衡,进而重塑老年免疫稳态。

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