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Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells

Nitric oxide (NO) regulates proliferation, differentiation and survival of neurons. Although NO is reported to involve in NGF-induced differentiation of PC12 cells, the role of NO has not been characterized in primary neuron cells. Therefore, we investigated the role of NO in neuronal differentiatio...

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Autores principales: Oh, Soo-Jin, Heo, Jee-In, Kho, Yoon-Jung, Kim, Jeong-Hyeon, Kang, Hong-Joon, Park, Seong-Hoon, Kim, Hyun-Seok, Shin, Jong-Yeon, Kim, Min-Ju, Kim, Sung Chan, Park, Jae-Bong, Kim, Jaebong, Lee, Jae-Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Brain and Neural Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214780/
https://www.ncbi.nlm.nih.gov/pubmed/22110346
http://dx.doi.org/10.5607/en.2010.19.2.83
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author Oh, Soo-Jin
Heo, Jee-In
Kho, Yoon-Jung
Kim, Jeong-Hyeon
Kang, Hong-Joon
Park, Seong-Hoon
Kim, Hyun-Seok
Shin, Jong-Yeon
Kim, Min-Ju
Kim, Sung Chan
Park, Jae-Bong
Kim, Jaebong
Lee, Jae-Yong
author_facet Oh, Soo-Jin
Heo, Jee-In
Kho, Yoon-Jung
Kim, Jeong-Hyeon
Kang, Hong-Joon
Park, Seong-Hoon
Kim, Hyun-Seok
Shin, Jong-Yeon
Kim, Min-Ju
Kim, Sung Chan
Park, Jae-Bong
Kim, Jaebong
Lee, Jae-Yong
author_sort Oh, Soo-Jin
collection PubMed
description Nitric oxide (NO) regulates proliferation, differentiation and survival of neurons. Although NO is reported to involve in NGF-induced differentiation of PC12 cells, the role of NO has not been characterized in primary neuron cells. Therefore, we investigated the role of NO in neuronal differentiation of primary cortical neuron cells. Primary cortical neuron cells were prepared from rat embryos of embryonic day 18 and treated with NMMA (NOS inhibitor) or PTIO (NO scavenger). Neurite outgrowth of neuron cells was counted and the mRNA levels of p21, p27, c-jun and c-myc were measured by RT-PCR. Neurite outgrowth of primary cortical neuron cells was inhibited a little by NOS inhibitor and completely by NO scavenger. The mRNA levels of p21 and p27, differentiation-induced growth arrest genes were increased during differentiation, but they were decreased by NOS inhibitor or NO scavenger. On the other hand, the level of c-jun mRNA was not changed and the level of c-myc mRNA was increased during differentiation differently from previously reported. The levels of these mRNA were reversed in NOS inhibitor- or NO scavenger-treated cells. The level of nNOS protein was not changed but NOS activity was inhibited largely by NOS inhibitor or NO scavenger. These results suggest that NO is an essential mediator for neuronal differentiation of primary cortical neuron cells.
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spelling pubmed-32147802011-11-22 Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells Oh, Soo-Jin Heo, Jee-In Kho, Yoon-Jung Kim, Jeong-Hyeon Kang, Hong-Joon Park, Seong-Hoon Kim, Hyun-Seok Shin, Jong-Yeon Kim, Min-Ju Kim, Sung Chan Park, Jae-Bong Kim, Jaebong Lee, Jae-Yong Exp Neurobiol Original Research Article Nitric oxide (NO) regulates proliferation, differentiation and survival of neurons. Although NO is reported to involve in NGF-induced differentiation of PC12 cells, the role of NO has not been characterized in primary neuron cells. Therefore, we investigated the role of NO in neuronal differentiation of primary cortical neuron cells. Primary cortical neuron cells were prepared from rat embryos of embryonic day 18 and treated with NMMA (NOS inhibitor) or PTIO (NO scavenger). Neurite outgrowth of neuron cells was counted and the mRNA levels of p21, p27, c-jun and c-myc were measured by RT-PCR. Neurite outgrowth of primary cortical neuron cells was inhibited a little by NOS inhibitor and completely by NO scavenger. The mRNA levels of p21 and p27, differentiation-induced growth arrest genes were increased during differentiation, but they were decreased by NOS inhibitor or NO scavenger. On the other hand, the level of c-jun mRNA was not changed and the level of c-myc mRNA was increased during differentiation differently from previously reported. The levels of these mRNA were reversed in NOS inhibitor- or NO scavenger-treated cells. The level of nNOS protein was not changed but NOS activity was inhibited largely by NOS inhibitor or NO scavenger. These results suggest that NO is an essential mediator for neuronal differentiation of primary cortical neuron cells. The Korean Society for Brain and Neural Science 2010-09 2010-09-30 /pmc/articles/PMC3214780/ /pubmed/22110346 http://dx.doi.org/10.5607/en.2010.19.2.83 Text en Copyright © Experimental Neurobiology 2010. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Oh, Soo-Jin
Heo, Jee-In
Kho, Yoon-Jung
Kim, Jeong-Hyeon
Kang, Hong-Joon
Park, Seong-Hoon
Kim, Hyun-Seok
Shin, Jong-Yeon
Kim, Min-Ju
Kim, Sung Chan
Park, Jae-Bong
Kim, Jaebong
Lee, Jae-Yong
Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells
title Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells
title_full Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells
title_fullStr Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells
title_full_unstemmed Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells
title_short Nitric Oxide Is an Essential Mediator for Neuronal Differentiation of Rat Primary Cortical Neuron Cells
title_sort nitric oxide is an essential mediator for neuronal differentiation of rat primary cortical neuron cells
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214780/
https://www.ncbi.nlm.nih.gov/pubmed/22110346
http://dx.doi.org/10.5607/en.2010.19.2.83
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