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通过 siRNA 技术和 2DE 联合 MALDI-TOF-TOF-MS 敲除 14-3-3τ 鉴定差异蛋白表达水平。

Differential protein expression level identification by knockout of 14-3-3τ with siRNA technique and 2DE followed MALDI-TOF-TOF-MS.

机构信息

Department of Chemistry, Fudan University, 220 Handan Road, Shanghai 200433, China.

出版信息

Analyst. 2011 Jan 21;136(2):401-6. doi: 10.1039/c0an00309c. Epub 2010 Nov 3.

DOI:10.1039/c0an00309c
PMID:21046037
Abstract

Cytotrophoblast cell differentiation into syncytiotrophoblast cells is a complex and delicate process, and the mechanism needs a large number of further studies. Knockout of 14-3-3τ expression and some further investigations were performed in the syncytiotrophoblast cell formation with RNA interference (RNAi) technology. The study found that the 14-3-3τ expression level with the formation of syncytiotrophoblast cells increased. Hypoxia inhibited the formation of syncytiotrophoblast cells where 14-3-3τ expression level decreased. RNAi reduced 14-3-3τ expression, and reduced the formation of syncytiotrophoblast cells. So that 14-3-3τ is not only involved in the cell regulation, but also in the formation of syncytiotrophoblast cells. 14-3-3τ is an important regulatory factor which inhibits the formation of hypoxia.

摘要

滋养细胞向合体滋养层细胞的分化是一个复杂而微妙的过程,其机制需要大量进一步的研究。利用 RNA 干扰(RNAi)技术在合胞体滋养层细胞形成过程中敲除 14-3-3τ 的表达并进行了一些进一步的研究。研究发现,14-3-3τ 的表达水平随合胞体滋养层细胞的形成而增加。缺氧抑制合胞体滋养层细胞的形成,导致 14-3-3τ 表达水平下降。RNAi 降低了 14-3-3τ 的表达,减少了合胞体滋养层细胞的形成。因此,14-3-3τ 不仅参与细胞调节,还参与合胞体滋养层细胞的形成。14-3-3τ 是抑制缺氧形成的重要调节因子。

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