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环磷酸腺苷(cAMP)诱导C6胶质瘤细胞分化过程中磷脂酶D(PLD)同工酶的mRNA差异表达。

Differential mRNA expression of phospholipase D (PLD) isozymes during cAMP-induced differentiation in C6 glioma cells.

作者信息

Yoshimura S, Nakashima S, Ohguchi K, Sakai H, Shinoda J, Sakai N, Nozawa Y

机构信息

Department of Neurosurgery, Gifu University School of Medicine, Japan.

出版信息

Biochem Biophys Res Commun. 1996 Aug 14;225(2):494-9. doi: 10.1006/bbrc.1996.1201.

Abstract

GTP gamma S-dependent phospholipase D (PLD) activity time-dependently increased during differentiation of rat C6 glioma cells to astrocytic phenotypes induced by dibutyryl cyclic AMP (dbcAMP)/theophylline. The changes in PLD mRNA level were examined by reverse transcriptase-polymerase chain reaction (RT-PCR) method using the degenerate primers designed based on two conserved amino acid sequences in PLDs of human and yeast. The amplified three DNA fragments (tentatively termed as rPLDa, b, and c) contained the conserved regions present in PLDs of various organisms. RT-PCR using non-degenerate primers showed that rPLDa mRNA increased within 12h following treatment with dbcAMP, reaching a broad plateau and then returned to the initial level at 48h. In contrast, the level of rPLDb mRNA showed a concurrent decrease. rPLDc decreased in a time-dependent manner. These results suggest that the expression of PLD mRNAs are differentially regulated during differentiation in C6 glioma cells.

摘要

在二丁酰环磷腺苷(dbcAMP)/茶碱诱导大鼠C6胶质瘤细胞向星形细胞表型分化的过程中,GTPγS依赖性磷脂酶D(PLD)活性随时间呈依赖性增加。采用基于人和酵母PLD中两个保守氨基酸序列设计的简并引物,通过逆转录-聚合酶链反应(RT-PCR)方法检测PLD mRNA水平的变化。扩增得到的三个DNA片段(暂称为rPLDa、b和c)包含了各种生物PLD中存在的保守区域。使用非简并引物的RT-PCR显示,dbcAMP处理后12小时内rPLDa mRNA增加,达到一个较宽的平台期,然后在48小时回到初始水平。相比之下,rPLDb mRNA水平同时下降。rPLDc呈时间依赖性下降。这些结果表明,C6胶质瘤细胞分化过程中PLD mRNAs的表达受到差异调节。

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