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脱铁转铁蛋白促进两种少突胶质细胞系的分化。

Apotransferrin promotes the differentiation of two oligodendroglial cell lines.

作者信息

Paez Pablo M, García Corina I, Davio Carlos, Campagnoni Anthony T, Soto Eduardo F, Pasquini Juana M

机构信息

Instituto de Química y Fisicoquímica Biológica (IQUIFIB), UBA-CONICET, Buenos Aires, Argentina.

出版信息

Glia. 2004 Apr 15;46(2):207-17. doi: 10.1002/glia.20001.

DOI:10.1002/glia.20001
PMID:15042587
Abstract

We have previously shown that addition of apotransferrin (aTf) accelerates maturation of oligodendroglial cells (OLGcs) in primary cultures. In this work, we examined the effect of aTf on two conditionally immortalized cell lines: N19 and N20.1. These cells proliferate at 34 degrees C and differentiate into mature OLGcs at 39 degrees C. In vitro addition of aTf to both cell lines at the differentiation temperature for 7 days showed increased expression of galactocerebroside, O4, and myelin basic protein (MBP) and a drop in the percentage of BrdU+ cells. The effect on MBP expression was particularly interesting in the less mature N19 cells. These cells do not express either MBP mRNAs or proteins, so aTf induced, rather than modulated, MBP expression in this cell line. In addition, even though MBP mRNAs for all four isoforms were induced, only the 17 and 21.5 kDa appeared to be translated. OLGc differentiation has been shown to be stimulated by the cAMP-CREB pathway. In N19 cells, following a pulse of aTf, there was a 10-fold increase in cAMP levels accompanied by elevated levels of pCREB. In the more mature N20.1 cells, there were no changes in cAMP levels. We conclude that addition of aTf to immature OLGc lines can enhance their expression of differentiated markers, such as MBP. The action of aTf on MBP gene expression in the least mature line is likely to be mediated by the cAMP pathway. In the N20.1 cells, it appears that different signals and/or mechanisms are involved in modulating myelin lipid and MBP expression. The results suggest that aTf can influence OLGc gene expression and differentiation through multiple mechanisms depending on the maturation of the cell.

摘要

我们之前已经表明,添加脱铁转铁蛋白(aTf)可加速原代培养中少突胶质细胞(OLGcs)的成熟。在这项研究中,我们检测了aTf对两种条件性永生化细胞系N19和N20.1的影响。这些细胞在34℃时增殖,并在39℃时分化为成熟的OLGcs。在分化温度下,于体外向这两种细胞系添加aTf 7天,结果显示半乳糖脑苷脂、O4和髓鞘碱性蛋白(MBP)的表达增加,且BrdU+细胞的百分比下降。对MBP表达的影响在不太成熟的N19细胞中尤为有趣。这些细胞既不表达MBP mRNA,也不表达MBP蛋白,因此aTf在该细胞系中诱导而非调节了MBP的表达。此外,尽管所有四种异构体的MBP mRNA都被诱导,但似乎只有17 kDa和21.5 kDa的MBP被翻译。OLGc的分化已被证明受cAMP-CREB途径刺激。在N19细胞中,aTf脉冲处理后,cAMP水平增加了10倍,同时pCREB水平升高。在更成熟的N20.1细胞中,cAMP水平没有变化。我们得出结论,向未成熟的OLGc系添加aTf可增强其分化标志物如MBP的表达。aTf对最不成熟细胞系中MBP基因表达的作用可能由cAMP途径介导。在N20.1细胞中,似乎不同的信号和/或机制参与了髓磷脂脂质和MBP表达的调节。结果表明,aTf可根据细胞的成熟程度通过多种机制影响OLGc的基因表达和分化。

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