Cargando…

Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions

Mutations in amyloid precursor protein (APP) have been most intensely studied in brain tissue for their link to Alzheimer’s disease (AD) pathology. However, APP is highly expressed in a variety of tissues including adipose tissue, where APP is also known to exhibit increased expression in response t...

Descripción completa

Detalles Bibliográficos
Autores principales: Freeman, Linnea R., Zhang, Le, Dasuri, Kalavathi, Fernandez-Kim, Sun-Ok, Bruce-Keller, Annadora J., Keller, Jeffrey N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422309/
https://www.ncbi.nlm.nih.gov/pubmed/22912823
http://dx.doi.org/10.1371/journal.pone.0043193
_version_ 1782241033981001728
author Freeman, Linnea R.
Zhang, Le
Dasuri, Kalavathi
Fernandez-Kim, Sun-Ok
Bruce-Keller, Annadora J.
Keller, Jeffrey N.
author_facet Freeman, Linnea R.
Zhang, Le
Dasuri, Kalavathi
Fernandez-Kim, Sun-Ok
Bruce-Keller, Annadora J.
Keller, Jeffrey N.
author_sort Freeman, Linnea R.
collection PubMed
description Mutations in amyloid precursor protein (APP) have been most intensely studied in brain tissue for their link to Alzheimer’s disease (AD) pathology. However, APP is highly expressed in a variety of tissues including adipose tissue, where APP is also known to exhibit increased expression in response to obesity. In our current study, we analyzed the effects of mutant APP (E693Q, D694N, K670N/M671L) expression toward multiple aspects of adipose tissue homeostasis. These data reveal significant hypoleptinemia, decreased adiposity, and reduced adipocyte size in response to mutant APP, and this was fully reversed upon high fat diet administration. Additionally, mutant APP was observed to significantly exacerbate insulin resistance, triglyceride elevations, and macrophage infiltration of adipose tissue in response to a high fat diet. Taken together, these data have significant implications for linking mutant APP expression to adipose tissue dysfunction and global changes in endocrine and metabolic function under both obesogenic and non-obesogenic conditions.
format Online
Article
Text
id pubmed-3422309
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34223092012-08-21 Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions Freeman, Linnea R. Zhang, Le Dasuri, Kalavathi Fernandez-Kim, Sun-Ok Bruce-Keller, Annadora J. Keller, Jeffrey N. PLoS One Research Article Mutations in amyloid precursor protein (APP) have been most intensely studied in brain tissue for their link to Alzheimer’s disease (AD) pathology. However, APP is highly expressed in a variety of tissues including adipose tissue, where APP is also known to exhibit increased expression in response to obesity. In our current study, we analyzed the effects of mutant APP (E693Q, D694N, K670N/M671L) expression toward multiple aspects of adipose tissue homeostasis. These data reveal significant hypoleptinemia, decreased adiposity, and reduced adipocyte size in response to mutant APP, and this was fully reversed upon high fat diet administration. Additionally, mutant APP was observed to significantly exacerbate insulin resistance, triglyceride elevations, and macrophage infiltration of adipose tissue in response to a high fat diet. Taken together, these data have significant implications for linking mutant APP expression to adipose tissue dysfunction and global changes in endocrine and metabolic function under both obesogenic and non-obesogenic conditions. Public Library of Science 2012-08-17 /pmc/articles/PMC3422309/ /pubmed/22912823 http://dx.doi.org/10.1371/journal.pone.0043193 Text en © 2012 Freeman et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Freeman, Linnea R.
Zhang, Le
Dasuri, Kalavathi
Fernandez-Kim, Sun-Ok
Bruce-Keller, Annadora J.
Keller, Jeffrey N.
Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
title Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
title_full Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
title_fullStr Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
title_full_unstemmed Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
title_short Mutant Amyloid Precursor Protein Differentially Alters Adipose Biology under Obesogenic and Non-Obesogenic Conditions
title_sort mutant amyloid precursor protein differentially alters adipose biology under obesogenic and non-obesogenic conditions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3422309/
https://www.ncbi.nlm.nih.gov/pubmed/22912823
http://dx.doi.org/10.1371/journal.pone.0043193
work_keys_str_mv AT freemanlinnear mutantamyloidprecursorproteindifferentiallyaltersadiposebiologyunderobesogenicandnonobesogenicconditions
AT zhangle mutantamyloidprecursorproteindifferentiallyaltersadiposebiologyunderobesogenicandnonobesogenicconditions
AT dasurikalavathi mutantamyloidprecursorproteindifferentiallyaltersadiposebiologyunderobesogenicandnonobesogenicconditions
AT fernandezkimsunok mutantamyloidprecursorproteindifferentiallyaltersadiposebiologyunderobesogenicandnonobesogenicconditions
AT brucekellerannadoraj mutantamyloidprecursorproteindifferentiallyaltersadiposebiologyunderobesogenicandnonobesogenicconditions
AT kellerjeffreyn mutantamyloidprecursorproteindifferentiallyaltersadiposebiologyunderobesogenicandnonobesogenicconditions