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Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study
Stem cell therapy is gaining attention as a promising treatment option for neurodegenerative diseases. The functional efficacy of grafted cells is a matter of debate and the recent consensus is that the cellular and functional recoveries might be due to “by-stander” effects of grafted cells. In the...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258312/ https://www.ncbi.nlm.nih.gov/pubmed/25505907 http://dx.doi.org/10.1155/2014/194967 |
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author | Bevinahal, Pradeep Kumar K. Venugopal, Chaitra Yencharla, Harish Chandra Prasad S. Chandanala, Shashank Trichur, Raju R. Talakad, Sathyaprabha N. Bhonde, Ramesh R. Dhanushkodi, Anandh |
author_facet | Bevinahal, Pradeep Kumar K. Venugopal, Chaitra Yencharla, Harish Chandra Prasad S. Chandanala, Shashank Trichur, Raju R. Talakad, Sathyaprabha N. Bhonde, Ramesh R. Dhanushkodi, Anandh |
author_sort | Bevinahal, Pradeep Kumar K. |
collection | PubMed |
description | Stem cell therapy is gaining attention as a promising treatment option for neurodegenerative diseases. The functional efficacy of grafted cells is a matter of debate and the recent consensus is that the cellular and functional recoveries might be due to “by-stander” effects of grafted cells. In the present study, we investigated the neuroprotective effect of conditioned medium (CM) derived from human embryonic kidney (HEK) cells in a kainic acid (KA) induced hippocampal degeneration model system in in vitro condition. Hippocampal cell line was exposed to KA (200 µM) for 24 hrs (lesion group) whereas, in the treatment group, hippocampal cell line was exposed to KA in combination with HEK-CM (KA + HEK-CM). We observed that KA exposure to cells resulted in significant neuronal loss. Interestingly, HEK-CM cotreatment completely attenuated the excitotoxic effects of KA. In HEK-CM cotreatment group, the cell viability was ~85–95% as opposed to 47% in KA alone group. Further investigation demonstrated that treatment with HEK-CM stimulated the endogenous cell survival factors like brain derived neurotrophic factors (BDNF) and antiapoptotic factor Bcl-2, revealing the possible mechanism of neuroprotection. Our results suggest that HEK-CM protects hippocampal neurons against excitotoxicity by stimulating the host's endogenous cell survival mechanisms. |
format | Online Article Text |
id | pubmed-4258312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42583122014-12-11 Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study Bevinahal, Pradeep Kumar K. Venugopal, Chaitra Yencharla, Harish Chandra Prasad S. Chandanala, Shashank Trichur, Raju R. Talakad, Sathyaprabha N. Bhonde, Ramesh R. Dhanushkodi, Anandh J Toxicol Research Article Stem cell therapy is gaining attention as a promising treatment option for neurodegenerative diseases. The functional efficacy of grafted cells is a matter of debate and the recent consensus is that the cellular and functional recoveries might be due to “by-stander” effects of grafted cells. In the present study, we investigated the neuroprotective effect of conditioned medium (CM) derived from human embryonic kidney (HEK) cells in a kainic acid (KA) induced hippocampal degeneration model system in in vitro condition. Hippocampal cell line was exposed to KA (200 µM) for 24 hrs (lesion group) whereas, in the treatment group, hippocampal cell line was exposed to KA in combination with HEK-CM (KA + HEK-CM). We observed that KA exposure to cells resulted in significant neuronal loss. Interestingly, HEK-CM cotreatment completely attenuated the excitotoxic effects of KA. In HEK-CM cotreatment group, the cell viability was ~85–95% as opposed to 47% in KA alone group. Further investigation demonstrated that treatment with HEK-CM stimulated the endogenous cell survival factors like brain derived neurotrophic factors (BDNF) and antiapoptotic factor Bcl-2, revealing the possible mechanism of neuroprotection. Our results suggest that HEK-CM protects hippocampal neurons against excitotoxicity by stimulating the host's endogenous cell survival mechanisms. Hindawi Publishing Corporation 2014 2014-11-23 /pmc/articles/PMC4258312/ /pubmed/25505907 http://dx.doi.org/10.1155/2014/194967 Text en Copyright © 2014 Pradeep Kumar K. Bevinahal et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Bevinahal, Pradeep Kumar K. Venugopal, Chaitra Yencharla, Harish Chandra Prasad S. Chandanala, Shashank Trichur, Raju R. Talakad, Sathyaprabha N. Bhonde, Ramesh R. Dhanushkodi, Anandh Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study |
title | Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study |
title_full | Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study |
title_fullStr | Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study |
title_full_unstemmed | Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study |
title_short | Conditioned Medium Reconditions Hippocampal Neurons against Kainic Acid Induced Excitotoxicity: An In Vitro Study |
title_sort | conditioned medium reconditions hippocampal neurons against kainic acid induced excitotoxicity: an in vitro study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4258312/ https://www.ncbi.nlm.nih.gov/pubmed/25505907 http://dx.doi.org/10.1155/2014/194967 |
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