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Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells
Astrocytes play a critical role in normal brain functions and maintaining the brain microenvironment, and defects in astrocytogenesis during neurodevelopment could give rise to severe mental illness and psychiatric disorders. During neuro-embryogenesis, astrocytogenesis involves astrocytic different...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society for Biochemistry and Molecular Biology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915117/ https://www.ncbi.nlm.nih.gov/pubmed/26645637 http://dx.doi.org/10.5483/BMBRep.2016.49.2.202 |
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author | Seo, Hyunhyo Lee, Kyungmin |
author_facet | Seo, Hyunhyo Lee, Kyungmin |
author_sort | Seo, Hyunhyo |
collection | PubMed |
description | Astrocytes play a critical role in normal brain functions and maintaining the brain microenvironment, and defects in astrocytogenesis during neurodevelopment could give rise to severe mental illness and psychiatric disorders. During neuro-embryogenesis, astrocytogenesis involves astrocytic differentiation of neural precursor cells (NPCs) induced by signals from ciliary neurotrophic factor (CNTF) or pituitary adenylate cyclase-activating peptide (PACAP). However, in contrast to the CNTF signaling pathway, the exact mechanism underlying astrocytic differentiation induced by PACAP is unknown. In the present study, we aimed to verify a signaling pathway specific to PACAP-induced astrocytogenesis, using exchange protein directly activated by cAMP2 (Epac2)-knockout mice. We found that PACAP could trigger astrocytic differentiation of NPCs via Epac2 activation and an increase in the intracellular calcium concentration via a calcium ion influx. Taken together, we concluded that astrocytogenesis stimulated by PACAP occurs through a novel signaling pathway independent from CNTF-JAK/STAT signaling, that is the well-known pathway of astrocytogenesis. [BMB Reports 2016; 49(2): 128-133] |
format | Online Article Text |
id | pubmed-4915117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Society for Biochemistry and Molecular Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-49151172016-06-23 Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells Seo, Hyunhyo Lee, Kyungmin BMB Rep Research-Article Astrocytes play a critical role in normal brain functions and maintaining the brain microenvironment, and defects in astrocytogenesis during neurodevelopment could give rise to severe mental illness and psychiatric disorders. During neuro-embryogenesis, astrocytogenesis involves astrocytic differentiation of neural precursor cells (NPCs) induced by signals from ciliary neurotrophic factor (CNTF) or pituitary adenylate cyclase-activating peptide (PACAP). However, in contrast to the CNTF signaling pathway, the exact mechanism underlying astrocytic differentiation induced by PACAP is unknown. In the present study, we aimed to verify a signaling pathway specific to PACAP-induced astrocytogenesis, using exchange protein directly activated by cAMP2 (Epac2)-knockout mice. We found that PACAP could trigger astrocytic differentiation of NPCs via Epac2 activation and an increase in the intracellular calcium concentration via a calcium ion influx. Taken together, we concluded that astrocytogenesis stimulated by PACAP occurs through a novel signaling pathway independent from CNTF-JAK/STAT signaling, that is the well-known pathway of astrocytogenesis. [BMB Reports 2016; 49(2): 128-133] Korean Society for Biochemistry and Molecular Biology 2016-02-29 /pmc/articles/PMC4915117/ /pubmed/26645637 http://dx.doi.org/10.5483/BMBRep.2016.49.2.202 Text en Copyright © 2016, Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research-Article Seo, Hyunhyo Lee, Kyungmin Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
title | Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
title_full | Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
title_fullStr | Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
title_full_unstemmed | Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
title_short | Epac2 contributes to PACAP-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
title_sort | epac2 contributes to pacap-induced astrocytic differentiation through calcium ion influx in neural precursor cells |
topic | Research-Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4915117/ https://www.ncbi.nlm.nih.gov/pubmed/26645637 http://dx.doi.org/10.5483/BMBRep.2016.49.2.202 |
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