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Global analysis of gene expression profiles in the submandibular salivary gland of klotho knockout mice.

Authors :
Kwon SM
Kim SA
Yoon JH
Yook JI
Ahn SG
Source :
Journal of cellular physiology [J Cell Physiol] 2018 Apr; Vol. 233 (4), pp. 3282-3294. Date of Electronic Publication: 2017 Sep 28.
Publication Year :
2018

Abstract

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 <superscript>+</superscript> /K <superscript>+</superscript> -ATPase (Atp1a2), Ca <superscript>2+</superscript> -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.<br /> (© 2017 The Authors. Journal of Cellular Physiology Published by Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1097-4652
Volume :
233
Issue :
4
Database :
MEDLINE
Journal :
Journal of cellular physiology
Publication Type :
Academic Journal
Accession number :
28885690
Full Text :
https://doi.org/10.1002/jcp.26172