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神经分泌能力。在PC12细胞中鉴定出的一个全面的基因表达程序。

Neurosecretion competence. A comprehensive gene expression program identified in PC12 cells.

作者信息

Grundschober Christophe, Malosio Maria Luisa, Astolfi Laura, Giordano Tiziana, Nef Patrick, Meldolesi Jacopo

机构信息

Central Nervous System, F. Hoffmann-La Roche Ltd., Grenzacherstrasse, Basel 4070, Switzerland.

出版信息

J Biol Chem. 2002 Sep 27;277(39):36715-24. doi: 10.1074/jbc.M203777200. Epub 2002 Jun 17.

Abstract

The phenotype of neurosecretory cells is characterized by clear vesicles and dense granules, both discharged by regulated exocytosis. However, these organelles are lacking completely in a few neurosecretion-incompetent clones of the pheochromocytoma PC12 line, in which other specific features are maintained (incompetent clones). In view of the heterogeneity of PC12 cells, a differential characterization of the incompetent phenotype based on the comparison of a single incompetent and a single wild-type clone would have been inconclusive. Therefore, we have compared two pairs of PC12 clones, studying in parallel the transcript levels of 4,200 genes and 19,000 express sequence tags (ESTs) by high density oligonucleotide arrays. After accurate data processing for quality control and filtration, a total of 755 transcripts, corresponding to 448 genes and 307 ESTs, was found consistently changed, with 46% up-regulated and 54% down-regulated in incompetent versus wild-type clones. Many but not all neurosecretion genes were profoundly down-regulated in incompetent cells. Expression of endocytosis genes was normal, whereas that of many nuclear and transcription factors, including some previously shown to play key roles in neurogenesis, was profoundly changed. Additional differences appeared in genes involved in signaling and metabolism. Taken together these results demonstrate for the first time that expression of neurosecretory vesicles and granules is part of a complex gene expression program that includes many other features that so far have not been recognized.

摘要

神经分泌细胞的表型特征是含有清亮小泡和致密颗粒,二者均通过调节性胞吐作用释放。然而,嗜铬细胞瘤PC12细胞系中一些无神经分泌能力的克隆完全缺乏这些细胞器,而这些克隆保留了其他特定特征(无能力克隆)。鉴于PC12细胞的异质性,基于单个无能力克隆和单个野生型克隆的比较对无能力表型进行差异表征可能无法得出结论。因此,我们比较了两对PC12克隆,通过高密度寡核苷酸阵列平行研究4200个基因和19000个表达序列标签(EST)的转录水平。经过精确的数据处理以进行质量控制和筛选后,共发现755个转录本持续变化,对应于448个基因和307个EST,在无能力克隆与野生型克隆中,46%上调,54%下调。许多但并非所有神经分泌基因在无能力细胞中均显著下调。内吞作用基因的表达正常,而许多核基因和转录因子的表达发生了显著变化,包括一些先前已证明在神经发生中起关键作用的因子。在参与信号传导和代谢的基因中也出现了其他差异。综上所述,这些结果首次证明神经分泌小泡和颗粒的表达是一个复杂基因表达程序的一部分,该程序还包括许多迄今尚未被认识的其他特征。

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