The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors
ABSTRACT: To assess the influence of the presenilin 1 (PS1) and 2 (PS2) mutations on amyloid deposition, neurofibrillary tangle (NFT) formation and neuronal loss, we performed stereologically based counts in a high-order association cortex, the superior temporal sulcus, of 30 familial Alzheimer'...
- Autores:
-
Gómez Isla, Teresa
Growdon, Whitfield B.
McNamara, Megan J.
Nochlin, David
Bird, Thomas D.
Arango Viana, Juan Carlos
Lopera Restrepo, Francisco Javier
Kosik, Kenneth S.
Lantos, Peter L.
Cairns, Nigel J.
Hyman, Bradley T.
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 1999
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/25831
- Acceso en línea:
- http://hdl.handle.net/10495/25831
- Palabra clave:
- Enfermedad de Alzheimer
Alzheimer Disease
Presenilina-1
Presenilin-1
Ovillos Neurofibrilares
Neurofibrillary Tangles
Presenilina-2
Presenilin-2
Aβ plaques
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc/2.5/co/
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oai:bibliotecadigital.udea.edu.co:10495/25831 |
network_acronym_str |
UDEA2 |
network_name_str |
Repositorio UdeA |
repository_id_str |
|
dc.title.spa.fl_str_mv |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
title |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
spellingShingle |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors Enfermedad de Alzheimer Alzheimer Disease Presenilina-1 Presenilin-1 Ovillos Neurofibrilares Neurofibrillary Tangles Presenilina-2 Presenilin-2 Aβ plaques |
title_short |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
title_full |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
title_fullStr |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
title_full_unstemmed |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
title_sort |
The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factors |
dc.creator.fl_str_mv |
Gómez Isla, Teresa Growdon, Whitfield B. McNamara, Megan J. Nochlin, David Bird, Thomas D. Arango Viana, Juan Carlos Lopera Restrepo, Francisco Javier Kosik, Kenneth S. Lantos, Peter L. Cairns, Nigel J. Hyman, Bradley T. |
dc.contributor.author.none.fl_str_mv |
Gómez Isla, Teresa Growdon, Whitfield B. McNamara, Megan J. Nochlin, David Bird, Thomas D. Arango Viana, Juan Carlos Lopera Restrepo, Francisco Javier Kosik, Kenneth S. Lantos, Peter L. Cairns, Nigel J. Hyman, Bradley T. |
dc.subject.decs.none.fl_str_mv |
Enfermedad de Alzheimer Alzheimer Disease Presenilina-1 Presenilin-1 Ovillos Neurofibrilares Neurofibrillary Tangles Presenilina-2 Presenilin-2 |
topic |
Enfermedad de Alzheimer Alzheimer Disease Presenilina-1 Presenilin-1 Ovillos Neurofibrilares Neurofibrillary Tangles Presenilina-2 Presenilin-2 Aβ plaques |
dc.subject.proposal.spa.fl_str_mv |
Aβ plaques |
description |
ABSTRACT: To assess the influence of the presenilin 1 (PS1) and 2 (PS2) mutations on amyloid deposition, neurofibrillary tangle (NFT) formation and neuronal loss, we performed stereologically based counts in a high-order association cortex, the superior temporal sulcus, of 30 familial Alzheimer's disease cases carrying 10 different PS1 and PS2 mutations, 51 sporadic Alzheimer's disease cases and 33 non-demented control subjects. All the PS1 and PS2 mutations assessed in this series led to enhanced deposition of total Aβ and Aβx-42/43 but not Aβx-40 senile plaques in the superior temporal sulcus when compared with brains from sporadic Alzheimer's disease patients. Some of the PS1 mutations studied (M139V, I143F, G209V, R269H, E280A), but not others, were also associated with faster rates of NFT formation and accelerated neuronal loss in the majority of the patients who harboured them when compared with sporadic Alzheimer's disease patients. In addition, our analysis showed that dramatic quantitative differences in clinical and neuropathological features can exist even among family members with the identical PS mutation. This suggests that further individual or pedigree genetic or epigenetic factors are likely to modulate PS phenotypes strongly. |
publishDate |
1999 |
dc.date.issued.none.fl_str_mv |
1999 |
dc.date.accessioned.none.fl_str_mv |
2022-02-07T16:22:50Z |
dc.date.available.none.fl_str_mv |
2022-02-07T16:22:50Z |
dc.type.spa.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.hasversion.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.redcol.spa.fl_str_mv |
https://purl.org/redcol/resource_type/ART |
dc.type.local.spa.fl_str_mv |
Artículo de investigación |
format |
http://purl.org/coar/resource_type/c_2df8fbb1 |
status_str |
publishedVersion |
dc.identifier.issn.none.fl_str_mv |
0006-8950 |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10495/25831 |
dc.identifier.eissn.none.fl_str_mv |
1460-2156 |
identifier_str_mv |
0006-8950 1460-2156 |
url |
http://hdl.handle.net/10495/25831 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Brain |
dc.rights.spa.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc/2.5/co/ |
dc.rights.accessrights.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.creativecommons.spa.fl_str_mv |
https://creativecommons.org/licenses/by-nc/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc/2.5/co/ http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by-nc/4.0/ |
dc.format.extent.spa.fl_str_mv |
11 |
dc.format.mimetype.spa.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Oxford University Press |
dc.publisher.group.spa.fl_str_mv |
Grupo de Investigación Clínica en Enfermedades del Niño y del Adolescente - Pediaciencias Grupo de Neurociencias de Antioquia |
dc.publisher.place.spa.fl_str_mv |
Londres, Inglaterra |
institution |
Universidad de Antioquia |
bitstream.url.fl_str_mv |
http://bibliotecadigital.udea.edu.co/bitstream/10495/25831/1/GomezTeresa_1999_ImpactDifferentPresenilin.pdf http://bibliotecadigital.udea.edu.co/bitstream/10495/25831/2/license_rdf http://bibliotecadigital.udea.edu.co/bitstream/10495/25831/3/license.txt |
bitstream.checksum.fl_str_mv |
c652ff66e2ece52055849964879bef99 c0c92b0ffc8b7d22d9cf56754a416a76 8a4605be74aa9ea9d79846c1fba20a33 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositorio Institucional Universidad de Antioquia |
repository.mail.fl_str_mv |
andres.perez@udea.edu.co |
_version_ |
1812173100624642048 |
spelling |
Gómez Isla, TeresaGrowdon, Whitfield B.McNamara, Megan J.Nochlin, DavidBird, Thomas D.Arango Viana, Juan CarlosLopera Restrepo, Francisco JavierKosik, Kenneth S.Lantos, Peter L.Cairns, Nigel J.Hyman, Bradley T.2022-02-07T16:22:50Z2022-02-07T16:22:50Z19990006-8950http://hdl.handle.net/10495/258311460-2156ABSTRACT: To assess the influence of the presenilin 1 (PS1) and 2 (PS2) mutations on amyloid deposition, neurofibrillary tangle (NFT) formation and neuronal loss, we performed stereologically based counts in a high-order association cortex, the superior temporal sulcus, of 30 familial Alzheimer's disease cases carrying 10 different PS1 and PS2 mutations, 51 sporadic Alzheimer's disease cases and 33 non-demented control subjects. All the PS1 and PS2 mutations assessed in this series led to enhanced deposition of total Aβ and Aβx-42/43 but not Aβx-40 senile plaques in the superior temporal sulcus when compared with brains from sporadic Alzheimer's disease patients. Some of the PS1 mutations studied (M139V, I143F, G209V, R269H, E280A), but not others, were also associated with faster rates of NFT formation and accelerated neuronal loss in the majority of the patients who harboured them when compared with sporadic Alzheimer's disease patients. In addition, our analysis showed that dramatic quantitative differences in clinical and neuropathological features can exist even among family members with the identical PS mutation. This suggests that further individual or pedigree genetic or epigenetic factors are likely to modulate PS phenotypes strongly.COL0058784COL001074411application/pdfengOxford University PressGrupo de Investigación Clínica en Enfermedades del Niño y del Adolescente - PediacienciasGrupo de Neurociencias de AntioquiaLondres, Inglaterrainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTArtículo de investigaciónhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc/2.5/co/http://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by-nc/4.0/The impact of different presenilin 1 and presenilin 2 mutations on amyloid pososition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain. Evidence for other phenotype-modifying factorsEnfermedad de AlzheimerAlzheimer DiseasePresenilina-1Presenilin-1Ovillos NeurofibrilaresNeurofibrillary TanglesPresenilina-2Presenilin-2Aβ plaquesBrainBrain170917191229ORIGINALGomezTeresa_1999_ImpactDifferentPresenilin.pdfGomezTeresa_1999_ImpactDifferentPresenilin.pdfArtículo de investigaciónapplication/pdf358890http://bibliotecadigital.udea.edu.co/bitstream/10495/25831/1/GomezTeresa_1999_ImpactDifferentPresenilin.pdfc652ff66e2ece52055849964879bef99MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8933http://bibliotecadigital.udea.edu.co/bitstream/10495/25831/2/license_rdfc0c92b0ffc8b7d22d9cf56754a416a76MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://bibliotecadigital.udea.edu.co/bitstream/10495/25831/3/license.txt8a4605be74aa9ea9d79846c1fba20a33MD5310495/25831oai:bibliotecadigital.udea.edu.co:10495/258312022-02-07 11:22:51.472Repositorio Institucional Universidad de Antioquiaandres.perez@udea.edu.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 |