Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)

The effects of quinacrine and minocycline on the toxicity induced by hPrP90-231 were studied. By mild thermal denaturation, hPrP90-231 can be converted in a toxic PrP<sup>Sc</sup>-like structure affecting the survival of SH-SY5Y cells. Quinacrine and minocycline prevented hPrP90-231-indu...

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Main Authors: V. Villa, A. Corsaro, S. Thellung, A. Simi, M. Nizzari, M. Tonelli, V. Boido, A. Aceto, T. Florio
Format: Article
Language:English
Published: PAGEPress Publications 2011-01-01
Series:Journal of Biological Research
Subjects:
Online Access:http://www.pagepressjournals.org/index.php/jbr/article/view/4689
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author V. Villa
A. Corsaro
S. Thellung
A. Simi
M. Nizzari
M. Tonelli
V. Boido
A. Aceto
T. Florio
author_facet V. Villa
A. Corsaro
S. Thellung
A. Simi
M. Nizzari
M. Tonelli
V. Boido
A. Aceto
T. Florio
author_sort V. Villa
collection DOAJ
description The effects of quinacrine and minocycline on the toxicity induced by hPrP90-231 were studied. By mild thermal denaturation, hPrP90-231 can be converted in a toxic PrP<sup>Sc</sup>-like structure affecting the survival of SH-SY5Y cells. Quinacrine and minocycline prevented hPrP90-231-induced toxicity interfering with different mechanisms: protective effects of quinacrine are mediated by the binding to the fragment that abolished hPrP90-231 structural changes and cell internalization, whereas, minocycline reverted MAP kinase neurotoxic signaling exerted by the prion fragment.
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spelling doaj.art-4de89126e8bb4db48737ffbd6150bb992022-12-21T23:05:15ZengPAGEPress PublicationsJournal of Biological Research1826-88382284-02302011-01-0184110.4081/jbr.2011.46893836Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)V. VillaA. CorsaroS. ThellungA. SimiM. NizzariM. TonelliV. BoidoA. AcetoT. FlorioThe effects of quinacrine and minocycline on the toxicity induced by hPrP90-231 were studied. By mild thermal denaturation, hPrP90-231 can be converted in a toxic PrP<sup>Sc</sup>-like structure affecting the survival of SH-SY5Y cells. Quinacrine and minocycline prevented hPrP90-231-induced toxicity interfering with different mechanisms: protective effects of quinacrine are mediated by the binding to the fragment that abolished hPrP90-231 structural changes and cell internalization, whereas, minocycline reverted MAP kinase neurotoxic signaling exerted by the prion fragment.http://www.pagepressjournals.org/index.php/jbr/article/view/4689prion protein, quinacrine, minocycline
spellingShingle V. Villa
A. Corsaro
S. Thellung
A. Simi
M. Nizzari
M. Tonelli
V. Boido
A. Aceto
T. Florio
Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)
Journal of Biological Research
prion protein, quinacrine, minocycline
title Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)
title_full Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)
title_fullStr Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)
title_full_unstemmed Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)
title_short Molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90-231 (hPrP90-231)
title_sort molecular mechanisms mediating the neuroproyective effects of quinacrine and minocycline on cell death induced by the prion protein fragment 90 231 hprp90 231
topic prion protein, quinacrine, minocycline
url http://www.pagepressjournals.org/index.php/jbr/article/view/4689
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