激活素A在小鼠和人胚胎畸胎癌细胞中的低表达。

Ontogenez Pub Date : 2014-07-01
O F Gordeeva
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引用次数: 0

摘要

TGFP3家族因子在调节小鼠和人多能干细胞和胚胎畸胎癌细胞的自我更新和分化平衡中发挥重要作用。TGFbeta家族信号配体在小鼠和人胚胎干细胞中的表达模式和这些信号通路的功能作用存在显著差异,但这些因子在小鼠和人胚胎畸胎癌细胞中的活性和功能作用尚未得到充分研究。通过实时荧光定量PCR对小鼠胚胎干细胞、胚胎胚和胚胎畸胎瘤细胞中TGF@[β]家族因子的表达进行比较,发现胚胎畸胎瘤细胞中ActivinA的表达水平低于多能干细胞,而Nodal、Lefty 1、TGFbeta1、BMP4、GDF3等因子的表达水平相近。在人无潜能性胚胎畸胎癌PA-1细胞中,TGFbeta家族的大多数因子(ACTIVINA、NODAL、LEFTY 1、BMP4和GDF3)的表达水平低于人胚胎干细胞:因此,在小鼠和人无潜能性畸胎癌细胞中,ACTIVINA的表达水平明显低于胚胎干细胞。据推测,这些差异可能与胚胎畸胎瘤细胞中各自信号通路功能活性的变化以及增殖和抗增殖机制的解除有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Low expression of activin A in mouse and human embryonic teratocarcinoma cells].

TGFP3 family factors play an important role in regulating the balance of self-renewal and differentiation of mouse and human pluripotent stem and embryonic teratocarcinoma cells. The expression patterns of TGFbeta family signaling ligands and functional roles of these signaling pathways differ significantly in mouse and human embryonic stem cells, but the activity and functional role of these factors in mouse and human embryonic teratocarcinoma cells were not sufficiently investigated. Comparative quantitative real-time PCR analysis of the expression of TGF@[beta] family factors in mouse embryonic stem, embryonic germ, and embryonic teratocarcinoma cells showed that embryonic teratocarcinoma cells express lower ActivinA than pluripotent stem cells but similar levels of factors Nodal, Lefty 1, TGFbeta1, BMP4, and GDF3. In human nullipotent embryonic teratocarcinoma PA-1 cells, most factors of the TGFbeta family (ACTIVINA, NODAL, LEFTY 1, BMP4, and GDF3) are expressed at lower levels than in human embryonic stem cells: Thus, in mouse and human nullipotent teratocarcinoma cells, theexpression of ActivinA is significantly reduced com- pared ivith embryonic stem cells. Presumably, these differences may be associated with changes in the functional activity of the respective signaling pathways and deregulation of proliferative and antiproliferative mechanisms in embryonic teratocarcinoma cells.

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