Prosaposin overexpression following kainic acid-induced neurotoxicity.

Because excessive glutamate release is believed to play a pivotal role in numerous neuropathological disorders, such as ischemia or seizure, we aimed to investigate whether intrinsic prosaposin (PS), a neuroprotective factor when supplied exogenously in vivo or in vitro, is up-regulated after the ex...

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Main Authors: Hiroaki Nabeka, Keigo Uematsu, Hiroko Takechi, Tetsuya Shimokawa, Kimiko Yamamiya, Cheng Li, Takuya Doihara, Shouichiro Saito, Naoto Kobayashi, Seiji Matsuda
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0110534
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author Hiroaki Nabeka
Keigo Uematsu
Hiroko Takechi
Tetsuya Shimokawa
Kimiko Yamamiya
Cheng Li
Takuya Doihara
Shouichiro Saito
Naoto Kobayashi
Seiji Matsuda
author_facet Hiroaki Nabeka
Keigo Uematsu
Hiroko Takechi
Tetsuya Shimokawa
Kimiko Yamamiya
Cheng Li
Takuya Doihara
Shouichiro Saito
Naoto Kobayashi
Seiji Matsuda
author_sort Hiroaki Nabeka
collection DOAJ
description Because excessive glutamate release is believed to play a pivotal role in numerous neuropathological disorders, such as ischemia or seizure, we aimed to investigate whether intrinsic prosaposin (PS), a neuroprotective factor when supplied exogenously in vivo or in vitro, is up-regulated after the excitotoxicity induced by kainic acid (KA), a glutamate analog. In the present study, PS immunoreactivity and its mRNA expression in the hippocampal and cortical neurons showed significant increases on day 3 after KA injection, and high PS levels were maintained even after 3 weeks. The increase in PS, but not saposins, detected by immunoblot analysis suggests that the increase in PS-like immunoreactivity after KA injection was not due to an increase in saposins as lysosomal enzymes after neuronal damage, but rather to an increase in PS as a neurotrophic factor to improve neuronal survival. Furthermore, several neurons with slender nuclei inside/outside of the pyramidal layer showed more intense PS mRNA expression than other pyramidal neurons. Based on the results from double immunostaining using anti-PS and anti-GABA antibodies, these neurons were shown to be GABAergic interneurons in the extra- and intra-pyramidal layers. In the cerebral cortex, several large neurons in the V layer showed very intense PS mRNA expression 3 days after KA injection. The choroid plexus showed intense PS mRNA expression even in the normal rat, and the intensity increased significantly after KA injection. The present study indicates that inhibitory interneurons as well as stimulated hippocampal pyramidal and cortical neurons synthesize PS for neuronal survival, and the choroid plexus is highly activated to synthesize PS, which may prevent neurons from excitotoxic neuronal damage. To the best of our knowledge, this is the first study that demonstrates axonal transport and increased production of neurotrophic factor PS after KA injection.
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spelling doaj.art-473ca402665b415a8b2109e4829aede62022-12-21T18:40:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11053410.1371/journal.pone.0110534Prosaposin overexpression following kainic acid-induced neurotoxicity.Hiroaki NabekaKeigo UematsuHiroko TakechiTetsuya ShimokawaKimiko YamamiyaCheng LiTakuya DoiharaShouichiro SaitoNaoto KobayashiSeiji MatsudaBecause excessive glutamate release is believed to play a pivotal role in numerous neuropathological disorders, such as ischemia or seizure, we aimed to investigate whether intrinsic prosaposin (PS), a neuroprotective factor when supplied exogenously in vivo or in vitro, is up-regulated after the excitotoxicity induced by kainic acid (KA), a glutamate analog. In the present study, PS immunoreactivity and its mRNA expression in the hippocampal and cortical neurons showed significant increases on day 3 after KA injection, and high PS levels were maintained even after 3 weeks. The increase in PS, but not saposins, detected by immunoblot analysis suggests that the increase in PS-like immunoreactivity after KA injection was not due to an increase in saposins as lysosomal enzymes after neuronal damage, but rather to an increase in PS as a neurotrophic factor to improve neuronal survival. Furthermore, several neurons with slender nuclei inside/outside of the pyramidal layer showed more intense PS mRNA expression than other pyramidal neurons. Based on the results from double immunostaining using anti-PS and anti-GABA antibodies, these neurons were shown to be GABAergic interneurons in the extra- and intra-pyramidal layers. In the cerebral cortex, several large neurons in the V layer showed very intense PS mRNA expression 3 days after KA injection. The choroid plexus showed intense PS mRNA expression even in the normal rat, and the intensity increased significantly after KA injection. The present study indicates that inhibitory interneurons as well as stimulated hippocampal pyramidal and cortical neurons synthesize PS for neuronal survival, and the choroid plexus is highly activated to synthesize PS, which may prevent neurons from excitotoxic neuronal damage. To the best of our knowledge, this is the first study that demonstrates axonal transport and increased production of neurotrophic factor PS after KA injection.https://doi.org/10.1371/journal.pone.0110534
spellingShingle Hiroaki Nabeka
Keigo Uematsu
Hiroko Takechi
Tetsuya Shimokawa
Kimiko Yamamiya
Cheng Li
Takuya Doihara
Shouichiro Saito
Naoto Kobayashi
Seiji Matsuda
Prosaposin overexpression following kainic acid-induced neurotoxicity.
PLoS ONE
title Prosaposin overexpression following kainic acid-induced neurotoxicity.
title_full Prosaposin overexpression following kainic acid-induced neurotoxicity.
title_fullStr Prosaposin overexpression following kainic acid-induced neurotoxicity.
title_full_unstemmed Prosaposin overexpression following kainic acid-induced neurotoxicity.
title_short Prosaposin overexpression following kainic acid-induced neurotoxicity.
title_sort prosaposin overexpression following kainic acid induced neurotoxicity
url https://doi.org/10.1371/journal.pone.0110534
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