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Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology

Peroxiredoxin 6 is an antioxidant enzyme and is the 1-cys member of the peroxiredoxin family. Using two-dimensional electrophoresis and Western blotting, we have shown for the first time that, in human control and brain tissue of patient’s with Alzheimer’s disease (AD), this enzyme exists as three m...

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Autores principales: Power, John H. T., Asad, Sana, Chataway, Tim K., Chegini, Fariba, Manavis, James, Temlett, James A., Jensen, Poul H., Blumbergs, Peter C., Gai, Wei-Ping
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386158/
https://www.ncbi.nlm.nih.gov/pubmed/18386021
http://dx.doi.org/10.1007/s00401-008-0373-3
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author Power, John H. T.
Asad, Sana
Chataway, Tim K.
Chegini, Fariba
Manavis, James
Temlett, James A.
Jensen, Poul H.
Blumbergs, Peter C.
Gai, Wei-Ping
author_facet Power, John H. T.
Asad, Sana
Chataway, Tim K.
Chegini, Fariba
Manavis, James
Temlett, James A.
Jensen, Poul H.
Blumbergs, Peter C.
Gai, Wei-Ping
author_sort Power, John H. T.
collection PubMed
description Peroxiredoxin 6 is an antioxidant enzyme and is the 1-cys member of the peroxiredoxin family. Using two-dimensional electrophoresis and Western blotting, we have shown for the first time that, in human control and brain tissue of patient’s with Alzheimer’s disease (AD), this enzyme exists as three major and five minor forms with pIs from 5.3 to 6.1. Using specific cellular markers, we have shown that peroxiredoxin 6 is present in astrocytes with very low levels in neurons, but not detectable in microglia or oligodendrocytes. In control brains, there was a very low level of peroxiredoxin 6 staining in astrocytes that was confined to a “halo” around the nucleus. In AD, there were marked increases in the number and staining intensity of peroxiredoxin 6 positive astrocytes in both gray and white matter in the midfrontal cortex, cingulate, hippocampus and amygdala. Confocal microscopy using antibodies to Aβ peptide, tau and peroxiredoxin 6 showed that peroxiredoxin 6 positive astrocytes are closely involved with diffuse plaques and to a lesser extent with neuritic plaques, suggesting that plaques are producing reactive oxygen species. There appeared to be little astrocytic response to tau containing neurons. Although peroxiredoxin 6 positive astrocytes were seen to make multiple contacts with tau positive neurons, there was no intraneuronal colocalization. In brain tissue of patients with AD, many blood vessels exhibited peroxiredoxin 6 staining that appeared to be due to the astrocytic foot processes. These results suggest that oxidative stress conditions exist in AD and that peroxiredoxin 6 is an important antioxidant enzyme in human brain defenses.
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spelling pubmed-23861582008-05-16 Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology Power, John H. T. Asad, Sana Chataway, Tim K. Chegini, Fariba Manavis, James Temlett, James A. Jensen, Poul H. Blumbergs, Peter C. Gai, Wei-Ping Acta Neuropathol Original Paper Peroxiredoxin 6 is an antioxidant enzyme and is the 1-cys member of the peroxiredoxin family. Using two-dimensional electrophoresis and Western blotting, we have shown for the first time that, in human control and brain tissue of patient’s with Alzheimer’s disease (AD), this enzyme exists as three major and five minor forms with pIs from 5.3 to 6.1. Using specific cellular markers, we have shown that peroxiredoxin 6 is present in astrocytes with very low levels in neurons, but not detectable in microglia or oligodendrocytes. In control brains, there was a very low level of peroxiredoxin 6 staining in astrocytes that was confined to a “halo” around the nucleus. In AD, there were marked increases in the number and staining intensity of peroxiredoxin 6 positive astrocytes in both gray and white matter in the midfrontal cortex, cingulate, hippocampus and amygdala. Confocal microscopy using antibodies to Aβ peptide, tau and peroxiredoxin 6 showed that peroxiredoxin 6 positive astrocytes are closely involved with diffuse plaques and to a lesser extent with neuritic plaques, suggesting that plaques are producing reactive oxygen species. There appeared to be little astrocytic response to tau containing neurons. Although peroxiredoxin 6 positive astrocytes were seen to make multiple contacts with tau positive neurons, there was no intraneuronal colocalization. In brain tissue of patients with AD, many blood vessels exhibited peroxiredoxin 6 staining that appeared to be due to the astrocytic foot processes. These results suggest that oxidative stress conditions exist in AD and that peroxiredoxin 6 is an important antioxidant enzyme in human brain defenses. Springer-Verlag 2008-04-02 2008-06 /pmc/articles/PMC2386158/ /pubmed/18386021 http://dx.doi.org/10.1007/s00401-008-0373-3 Text en © Springer-Verlag 2008
spellingShingle Original Paper
Power, John H. T.
Asad, Sana
Chataway, Tim K.
Chegini, Fariba
Manavis, James
Temlett, James A.
Jensen, Poul H.
Blumbergs, Peter C.
Gai, Wei-Ping
Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology
title Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology
title_full Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology
title_fullStr Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology
title_full_unstemmed Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology
title_short Peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with Alzheimer’s disease pathology
title_sort peroxiredoxin 6 in human brain: molecular forms, cellular distribution and association with alzheimer’s disease pathology
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2386158/
https://www.ncbi.nlm.nih.gov/pubmed/18386021
http://dx.doi.org/10.1007/s00401-008-0373-3
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