Literature DB >> 11117517

PrP fragment 106-126 is toxic to cerebral endothelial cells expressing PrP(C).

M A Deli1, S Sakaguchi, R Nakaoke, C S Abrahám, H Takahata, J Kopacek, K Shigematsu, S Katamine, M Niwa.   

Abstract

A hydrophobic, fibrillogenic peptide fragment of human prion protein (PrP106-126) had in vitro toxicity to neurons expressing cellular prion protein (PrP(C)). In this study, we proved that primary cultures of mouse cerebral endothelial cells (MCEC) express PrP(C). Incubation of MCEC with PrP106-126 (25-200 microM) caused a dose-dependent toxicity assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, lactate dehydrogenase release, bis-benzimide staining for nuclear morphology, and trypan blue exclusion test. Pentosan polysulphate (50-100 microg/ml), a drug effective in scrapie prophylaxis, dose-dependently attenuated the injury. MCEC cultures from mice homogenous for the disrupted PrP gene were resistant to the toxicity of PrP106-126. In conclusion, cerebral endothelium expressing PrP(C) may be directly damaged during spongiform encephalopathies.

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Year:  2000        PMID: 11117517     DOI: 10.1097/00001756-200011270-00064

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  10 in total

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Review 2.  In vitro methods in the study of viral and prion permeability across the blood-brain barrier.

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Review 8.  Surface charge, glycocalyx, and blood-brain barrier function.

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9.  Age influences susceptibility of brain capillary endothelial cells to La Crosse virus infection and cell death.

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10.  Low dose cranial irradiation-induced cerebrovascular damage is reversible in mice.

Authors:  Nikolett Sándor; Fruzsina R Walter; Alexandra Bocsik; Petra Sántha; Boglárka Schilling-Tóth; Violetta Léner; Zoltán Varga; Zsuzsanna Kahán; Mária A Deli; Géza Sáfrány; Hargita Hegyesi
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  10 in total

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