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Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats
Hepatocyte growth factor (HGF) has neuroprotective effects against ischemia-induced injuries. Dental pulp stem cell (DPSC) transplantation attenuates tissue injury in the brain of rats with post-transient middle cerebral artery occlusion. We sought to determine whether DPSCs that overexpress HGF can...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108066/ https://www.ncbi.nlm.nih.gov/pubmed/30151417 http://dx.doi.org/10.1016/j.omtm.2018.07.009 |
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author | Sowa, Kota Nito, Chikako Nakajima, Masataka Suda, Satoshi Nishiyama, Yasuhiro Sakamoto, Yuki Nitahara-Kasahara, Yuko Nakamura-Takahashi, Aki Ueda, Masayuki Kimura, Kazumi Okada, Takashi |
author_facet | Sowa, Kota Nito, Chikako Nakajima, Masataka Suda, Satoshi Nishiyama, Yasuhiro Sakamoto, Yuki Nitahara-Kasahara, Yuko Nakamura-Takahashi, Aki Ueda, Masayuki Kimura, Kazumi Okada, Takashi |
author_sort | Sowa, Kota |
collection | PubMed |
description | Hepatocyte growth factor (HGF) has neuroprotective effects against ischemia-induced injuries. Dental pulp stem cell (DPSC) transplantation attenuates tissue injury in the brain of rats with post-transient middle cerebral artery occlusion. We sought to determine whether DPSCs that overexpress HGF can enhance their therapeutic effects on brain damage post-ischemia/reperfusion injury. Treatment with DPSCs overexpressing HGF reduced infarct volumes compared to unmodified DPSC treatment at 3 and 7 days post-transient middle cerebral artery occlusion. The use of unmodified DPSCs and DPSCs overexpressing HGF was associated with improved motor function compared to that with administration of vehicle at 7 days post-transient middle cerebral artery occlusion. DPSCs overexpressing HGF significantly inhibited microglial activation and pro-inflammatory cytokine production along with suppression of neuronal degeneration. Post-reperfusion, DPSCs overexpressing HGF attenuated the decreases in tight junction proteins, maintained blood-brain barrier integrity, and increased microvessel density in peri-infarct areas. The administration of DPSCs overexpressing HGF during the acute phase of stroke increased their neuroprotective effects by modulating inflammation and blood-brain barrier permeability, thereby promoting improvements in post-ischemia/reperfusion brain injury. |
format | Online Article Text |
id | pubmed-6108066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-61080662018-08-27 Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats Sowa, Kota Nito, Chikako Nakajima, Masataka Suda, Satoshi Nishiyama, Yasuhiro Sakamoto, Yuki Nitahara-Kasahara, Yuko Nakamura-Takahashi, Aki Ueda, Masayuki Kimura, Kazumi Okada, Takashi Mol Ther Methods Clin Dev Article Hepatocyte growth factor (HGF) has neuroprotective effects against ischemia-induced injuries. Dental pulp stem cell (DPSC) transplantation attenuates tissue injury in the brain of rats with post-transient middle cerebral artery occlusion. We sought to determine whether DPSCs that overexpress HGF can enhance their therapeutic effects on brain damage post-ischemia/reperfusion injury. Treatment with DPSCs overexpressing HGF reduced infarct volumes compared to unmodified DPSC treatment at 3 and 7 days post-transient middle cerebral artery occlusion. The use of unmodified DPSCs and DPSCs overexpressing HGF was associated with improved motor function compared to that with administration of vehicle at 7 days post-transient middle cerebral artery occlusion. DPSCs overexpressing HGF significantly inhibited microglial activation and pro-inflammatory cytokine production along with suppression of neuronal degeneration. Post-reperfusion, DPSCs overexpressing HGF attenuated the decreases in tight junction proteins, maintained blood-brain barrier integrity, and increased microvessel density in peri-infarct areas. The administration of DPSCs overexpressing HGF during the acute phase of stroke increased their neuroprotective effects by modulating inflammation and blood-brain barrier permeability, thereby promoting improvements in post-ischemia/reperfusion brain injury. American Society of Gene & Cell Therapy 2018-08-04 /pmc/articles/PMC6108066/ /pubmed/30151417 http://dx.doi.org/10.1016/j.omtm.2018.07.009 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Sowa, Kota Nito, Chikako Nakajima, Masataka Suda, Satoshi Nishiyama, Yasuhiro Sakamoto, Yuki Nitahara-Kasahara, Yuko Nakamura-Takahashi, Aki Ueda, Masayuki Kimura, Kazumi Okada, Takashi Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats |
title | Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats |
title_full | Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats |
title_fullStr | Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats |
title_full_unstemmed | Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats |
title_short | Impact of Dental Pulp Stem Cells Overexpressing Hepatocyte Growth Factor after Cerebral Ischemia/Reperfusion in Rats |
title_sort | impact of dental pulp stem cells overexpressing hepatocyte growth factor after cerebral ischemia/reperfusion in rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6108066/ https://www.ncbi.nlm.nih.gov/pubmed/30151417 http://dx.doi.org/10.1016/j.omtm.2018.07.009 |
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