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Timing-Dependent Actions of NGF Required for Cell Differentiation

BACKGROUND: Continuous NGF stimulation induces PC12 cell differentiation. However, why continuous NGF stimulation is required for differentiation is unclear. In this study, we investigated the underlying mechanisms of the timing-dependent requirement of NGF action for cell differentiation. METHODOLO...

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Autores principales: Chung, Jaehoon, Kubota, Hiroyuki, Ozaki, Yu-ichi, Uda, Shinsuke, Kuroda, Shinya
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814856/
https://www.ncbi.nlm.nih.gov/pubmed/20126402
http://dx.doi.org/10.1371/journal.pone.0009011
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author Chung, Jaehoon
Kubota, Hiroyuki
Ozaki, Yu-ichi
Uda, Shinsuke
Kuroda, Shinya
author_facet Chung, Jaehoon
Kubota, Hiroyuki
Ozaki, Yu-ichi
Uda, Shinsuke
Kuroda, Shinya
author_sort Chung, Jaehoon
collection PubMed
description BACKGROUND: Continuous NGF stimulation induces PC12 cell differentiation. However, why continuous NGF stimulation is required for differentiation is unclear. In this study, we investigated the underlying mechanisms of the timing-dependent requirement of NGF action for cell differentiation. METHODOLOGY/PRINCIPAL FINDINGS: To address the timing-dependency of the NGF action, we performed a discontinuous stimulation assay consisting of a first transient stimulation followed by an interval and then a second sustained stimulation and quantified the neurite extension level. Consequently, we observed a timing-dependent action of NGF on cell differentiation, and discontinuous NGF stimulation similarly induced differentiation. The first stimulation did not induce neurite extension, whereas the second stimulation induced fast neurite extension; therefore, the first stimulation is likely required as a prerequisite condition. These observations indicate that the action of NGF can be divided into two processes: an initial stimulation-driven latent process and a second stimulation-driven extension process. The latent process appears to require the activities of ERK and transcription, but not PI3K, whereas the extension-process requires the activities of ERK and PI3K, but not transcription. We also found that during the first stimulation, the activity of NGF can be replaced by PACAP, but not by insulin, EGF, bFGF or forskolin; during the second stimulation, however, the activity of NGF cannot be replaced by any of these stimulants. These findings allowed us to identify potential genes specifically involved in the latent process, rather than in other processes, using a microarray. CONCLUSIONS/SIGNIFICANCE: These results demonstrate that NGF induces the differentiation of PC12 cells via mechanically distinct processes: an ERK-driven and transcription-dependent latent process, and an ERK- and PI3K-driven and transcription-independent extension process.
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spelling pubmed-28148562010-02-03 Timing-Dependent Actions of NGF Required for Cell Differentiation Chung, Jaehoon Kubota, Hiroyuki Ozaki, Yu-ichi Uda, Shinsuke Kuroda, Shinya PLoS One Research Article BACKGROUND: Continuous NGF stimulation induces PC12 cell differentiation. However, why continuous NGF stimulation is required for differentiation is unclear. In this study, we investigated the underlying mechanisms of the timing-dependent requirement of NGF action for cell differentiation. METHODOLOGY/PRINCIPAL FINDINGS: To address the timing-dependency of the NGF action, we performed a discontinuous stimulation assay consisting of a first transient stimulation followed by an interval and then a second sustained stimulation and quantified the neurite extension level. Consequently, we observed a timing-dependent action of NGF on cell differentiation, and discontinuous NGF stimulation similarly induced differentiation. The first stimulation did not induce neurite extension, whereas the second stimulation induced fast neurite extension; therefore, the first stimulation is likely required as a prerequisite condition. These observations indicate that the action of NGF can be divided into two processes: an initial stimulation-driven latent process and a second stimulation-driven extension process. The latent process appears to require the activities of ERK and transcription, but not PI3K, whereas the extension-process requires the activities of ERK and PI3K, but not transcription. We also found that during the first stimulation, the activity of NGF can be replaced by PACAP, but not by insulin, EGF, bFGF or forskolin; during the second stimulation, however, the activity of NGF cannot be replaced by any of these stimulants. These findings allowed us to identify potential genes specifically involved in the latent process, rather than in other processes, using a microarray. CONCLUSIONS/SIGNIFICANCE: These results demonstrate that NGF induces the differentiation of PC12 cells via mechanically distinct processes: an ERK-driven and transcription-dependent latent process, and an ERK- and PI3K-driven and transcription-independent extension process. Public Library of Science 2010-02-02 /pmc/articles/PMC2814856/ /pubmed/20126402 http://dx.doi.org/10.1371/journal.pone.0009011 Text en Chung et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Chung, Jaehoon
Kubota, Hiroyuki
Ozaki, Yu-ichi
Uda, Shinsuke
Kuroda, Shinya
Timing-Dependent Actions of NGF Required for Cell Differentiation
title Timing-Dependent Actions of NGF Required for Cell Differentiation
title_full Timing-Dependent Actions of NGF Required for Cell Differentiation
title_fullStr Timing-Dependent Actions of NGF Required for Cell Differentiation
title_full_unstemmed Timing-Dependent Actions of NGF Required for Cell Differentiation
title_short Timing-Dependent Actions of NGF Required for Cell Differentiation
title_sort timing-dependent actions of ngf required for cell differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2814856/
https://www.ncbi.nlm.nih.gov/pubmed/20126402
http://dx.doi.org/10.1371/journal.pone.0009011
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