Prolyl Endopeptidase Is Involved in Cellular Signalling in Human Neuroblastoma SH-SY5Y Cells

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 differ...

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Veröffentlicht in:Neuro-Signals 2011, Vol.19 (2), p.97-109
Hauptverfasser: Moreno-Baylach, M. José, Puttonen, Katja A., Tenorio-Laranga, Jofre, Venäläinen, Jarkko I., Storvik, Markus, Forsberg, Markus M., García-Horsman, J. Arturo
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container_end_page 109
container_issue 2
container_start_page 97
container_title Neuro-Signals
container_volume 19
creator Moreno-Baylach, M. José
Puttonen, Katja A.
Tenorio-Laranga, Jofre
Venäläinen, Jarkko I.
Storvik, Markus
Forsberg, Markus M.
García-Horsman, J. Arturo
description 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.
doi_str_mv 10.1159/000326342
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José ; Puttonen, Katja A. ; Tenorio-Laranga, Jofre ; Venäläinen, Jarkko I. ; Storvik, Markus ; Forsberg, Markus M. ; García-Horsman, J. Arturo</creator><creatorcontrib>Moreno-Baylach, M. José ; Puttonen, Katja A. ; Tenorio-Laranga, Jofre ; Venäläinen, Jarkko I. ; Storvik, Markus ; Forsberg, Markus M. ; García-Horsman, J. Arturo</creatorcontrib><description>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. 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José</creatorcontrib><creatorcontrib>Puttonen, Katja A.</creatorcontrib><creatorcontrib>Tenorio-Laranga, Jofre</creatorcontrib><creatorcontrib>Venäläinen, Jarkko I.</creatorcontrib><creatorcontrib>Storvik, Markus</creatorcontrib><creatorcontrib>Forsberg, Markus M.</creatorcontrib><creatorcontrib>García-Horsman, J. Arturo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Neuro-Signals</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moreno-Baylach, M. José</au><au>Puttonen, Katja A.</au><au>Tenorio-Laranga, Jofre</au><au>Venäläinen, Jarkko I.</au><au>Storvik, Markus</au><au>Forsberg, Markus M.</au><au>García-Horsman, J. 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subjects Cell Line, Tumor
Humans
Mitochondrial Proteins - genetics
Mitochondrial Proteins - metabolism
Neuroblastoma - enzymology
Neuroblastoma - pathology
Neurons - enzymology
Neurons - pathology
Original Paper
Serine Endopeptidases - genetics
Serine Endopeptidases - metabolism
Signal Transduction - drug effects
Signal Transduction - physiology
title Prolyl Endopeptidase Is Involved in Cellular Signalling in Human Neuroblastoma SH-SY5Y Cells
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