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Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice
Salivary dysfunction commonly occurs in many older adults and is considered a physiological phenomenon. However, the genetic changes in salivary glands during aging have not been characterized. The present study analyzed the gene expression profile in salivary glands from accelerated aging klotho de...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765504/ https://www.ncbi.nlm.nih.gov/pubmed/28885690 http://dx.doi.org/10.1002/jcp.26172 |
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author | Kwon, Sung‐Min Kim, Soo‐A Yoon, Jung‐Hoon Yook, Jong‐In Ahn, Sang‐Gun |
author_facet | Kwon, Sung‐Min Kim, Soo‐A Yoon, Jung‐Hoon Yook, Jong‐In Ahn, Sang‐Gun |
author_sort | Kwon, Sung‐Min |
collection | PubMed |
description | Salivary dysfunction commonly occurs in many older adults and is considered a physiological phenomenon. However, the genetic changes in salivary glands during aging have not been characterized. The present study analyzed the gene expression profile in salivary glands from accelerated aging klotho deficient mice (klotho−/−, 4 weeks old). Microarray analysis showed that 195 genes were differentially expressed (z‐score > 2 in two independent arrays) in klotho null mice compared to wild‐type mice. Importantly, alpha2‐Na(+)/K(+)‐ATPase (Atp1a2), Ca(2+)‐ATPase (Atp2a1), epidermal growth factor (EGF), and nerve growth factor (NGF), which have been suggested to be regulators of submandibular salivary gland function, were significantly decreased. When a network was constructed from the differentially expressed genes, proliferator‐activated receptor‐γ (PPAR γ), which regulates energy homeostasis and insulin sensitivity, was located at the core of the network. In addition, the expression of genes proposed to regulate various PPAR γ‐related cellular pathways, such as Klk1b26, Egfbp2, Cox8b, Gpx3, Fabp3, EGF, and NGFβ, was altered in the submandibular salivary glands of klotho−/− mice. Our results may provide clues for the identification of novel genes involved in salivary gland dysfunction. Further characterization of these differentially expressed genes will be useful in elucidating the genetic basis of aging‐related changes in the submandibular salivary gland. |
format | Online Article Text |
id | pubmed-5765504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57655042018-02-01 Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice Kwon, Sung‐Min Kim, Soo‐A Yoon, Jung‐Hoon Yook, Jong‐In Ahn, Sang‐Gun J Cell Physiol Original Research Articles Salivary dysfunction commonly occurs in many older adults and is considered a physiological phenomenon. However, the genetic changes in salivary glands during aging have not been characterized. The present study analyzed the gene expression profile in salivary glands from accelerated aging klotho deficient mice (klotho−/−, 4 weeks old). Microarray analysis showed that 195 genes were differentially expressed (z‐score > 2 in two independent arrays) in klotho null mice compared to wild‐type mice. Importantly, alpha2‐Na(+)/K(+)‐ATPase (Atp1a2), Ca(2+)‐ATPase (Atp2a1), epidermal growth factor (EGF), and nerve growth factor (NGF), which have been suggested to be regulators of submandibular salivary gland function, were significantly decreased. When a network was constructed from the differentially expressed genes, proliferator‐activated receptor‐γ (PPAR γ), which regulates energy homeostasis and insulin sensitivity, was located at the core of the network. In addition, the expression of genes proposed to regulate various PPAR γ‐related cellular pathways, such as Klk1b26, Egfbp2, Cox8b, Gpx3, Fabp3, EGF, and NGFβ, was altered in the submandibular salivary glands of klotho−/− mice. Our results may provide clues for the identification of novel genes involved in salivary gland dysfunction. Further characterization of these differentially expressed genes will be useful in elucidating the genetic basis of aging‐related changes in the submandibular salivary gland. John Wiley and Sons Inc. 2017-09-28 2018-04 /pmc/articles/PMC5765504/ /pubmed/28885690 http://dx.doi.org/10.1002/jcp.26172 Text en © 2017 The Authors. Journal of Cellular Physiology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Articles Kwon, Sung‐Min Kim, Soo‐A Yoon, Jung‐Hoon Yook, Jong‐In Ahn, Sang‐Gun Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
title | Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
title_full | Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
title_fullStr | Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
title_full_unstemmed | Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
title_short | Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
title_sort | global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5765504/ https://www.ncbi.nlm.nih.gov/pubmed/28885690 http://dx.doi.org/10.1002/jcp.26172 |
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