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锂离子上调神经生长因子分化的PC12细胞中编码致密核心囊泡蛋白的mRNA。

Lithium ions Up-regulate mRNAs encoding dense-core vesicle proteins in nerve growth factor-differentiated PC12 cells.

作者信息

Cordeiro M L, Umbach J A, Gundersen C B

机构信息

Department of Molecular and Medical Pharmacology and Crump Institute for Molecular Imaging, School of Medicine, University of California Los Angeles 90095-1770, USA.

出版信息

J Neurochem. 2000 Dec;75(6):2622-5. doi: 10.1046/j.1471-4159.2000.0752622.x.

Abstract

We recently reported that lithium ions induced an up-regulation of cysteine string protein (CSP) gene expression in nerve growth factor (NGF)-differentiated PC12 cells but not in undifferentiated cells. Concomitantly, expression of two other proteins of regulated secretory pathways, synaptophysin (SY) and SNAP-25, was unaffected by lithium. To assess further the specificity of this effect of lithium, we used cDNA arrays. Our data indicate that lithium ions increase the level of mRNA for proteins such as secretogranin II and vesicular monoamine transporter 1 that are preferentially associated with large densecore secretory vesicles (LDCVs) without affecting mRNAs for proteins predominantly affiliated with small synaptic-like vesicles, including the vesicular acetylcholine transporter and SY. This action of lithium is detected in NGF-differentiated PC12 cells but not in undifferentiated cells. These observations suggest that lithium ions modulate the turnover of LDCVs, and this may play a role in mediating the therapeutic action of lithium in manic-depressive illness.

摘要

我们最近报道,锂离子可诱导神经生长因子(NGF)分化的PC12细胞中半胱氨酸串珠蛋白(CSP)基因表达上调,但未分化细胞中则不会。同时,另外两种受调节分泌途径的蛋白,即突触素(SY)和SNAP-25的表达不受锂的影响。为了进一步评估锂这种作用的特异性,我们使用了cDNA阵列。我们的数据表明,锂离子可增加诸如分泌粒蛋白II和囊泡单胺转运体1等蛋白的mRNA水平,这些蛋白优先与大致密核心分泌囊泡(LDCV)相关,而不影响主要与小突触样囊泡相关的蛋白的mRNA,包括囊泡乙酰胆碱转运体和SY。锂的这种作用在NGF分化的PC12细胞中可检测到,但在未分化细胞中则未检测到。这些观察结果表明,锂离子可调节LDCV的周转,这可能在介导锂在躁狂抑郁症中的治疗作用中发挥作用。

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