Moreno-Baylach M José, Puttonen Katja A, Tenorio-Laranga Jofre, Venäläinen Jarkko I, Storvik Markus, Forsberg Markus M, García-Horsman J Arturo
Division of Pharmacology and Toxicology, University of Helsinki, Helsinki, Finland.
Neurosignals. 2011;19(2):97-109. doi: 10.1159/000326342. Epub 2011 Apr 10.
Prolyl endopeptidase (PREP), probably acting through the inositol cycle, has been implicated in memory and learning. However, the physiological role of PREP is unknown. It has been shown that PREP expression, regulated in cerebellar granule cells, has probably a role in cell proliferation and differentiation. Here, we report the levels and subcellular distribution of PREP in human neuroblastoma SH-SY5Y cells in proliferating conditions and under differentiation induced by retinoic acid (RA). We analysed the levels of cell signalling intermediates, growth behavior and gene expression, and differentiation morphology changes, upon PREP inhibition. After induction of differentiation, PREP activity was found decreased in the nucleus but increased to high levels in the cytoplasm, due in part to increased PREP transcription. The levels of inositol (1,4,5)-trisphosphate revealed no correlation with PREP activity, but phosphorylated extracellular signal-regulated kinases 1 and 2 were decreased by PREP inhibition during early stages of differentiation. Morphological evaluation indicated that PREP inhibition retarded the onset of differentiation. PREP activity regulated gene expression of protein synthesis machinery, intracellular transport and kinase complexes. We conclude that PREP is a regulatory target and a regulatory element in cell signalling. This is the first report of a direct influence of a cell signalling molecule, RA, on PREP expression.
脯氨酰内肽酶(PREP)可能通过肌醇循环发挥作用,与记忆和学习有关。然而,PREP的生理作用尚不清楚。研究表明,在小脑颗粒细胞中受调控的PREP表达可能在细胞增殖和分化中发挥作用。在此,我们报告了在增殖条件下以及视黄酸(RA)诱导分化的情况下,人神经母细胞瘤SH-SY5Y细胞中PREP的水平和亚细胞分布。我们分析了PREP抑制后细胞信号中间体的水平、生长行为和基因表达以及分化形态变化。诱导分化后,发现PREP活性在细胞核中降低,但在细胞质中升高至高水平,部分原因是PREP转录增加。肌醇(1,4,5)-三磷酸的水平与PREP活性无相关性,但在分化早期,PREP抑制可使磷酸化的细胞外信号调节激酶1和2减少。形态学评估表明,PREP抑制延迟了分化的开始。PREP活性调节蛋白质合成机制、细胞内运输和激酶复合物的基因表达。我们得出结论,PREP是细胞信号传导中的一个调节靶点和调节元件。这是关于细胞信号分子RA对PREP表达直接影响的首次报道。