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Soluble levels and endogenous vascular gene expression of KLOTHO are related to inflammation in human atherosclerotic disease.
- Source :
-
Clinical science (London, England : 1979) [Clin Sci (Lond)] 2017 Oct 25; Vol. 131 (21), pp. 2601-2609. Date of Electronic Publication: 2017 Oct 25 (Print Publication: 2017). - Publication Year :
- 2017
-
Abstract
- Atherosclerosis is a chronic inflammatory disorder affecting the artery wall. Klotho, an anti-aging factor expressed in the vessel walls that participates in the maintenance of vascular homeostasis, can be down-regulated by inflammation. In this proof-of-concept work we seek to characterize the arterial KLOTHO expression in the vascular wall, as well as the serum concentration of this protein, in a group of patients with clinical atherosclerotic disease. In addition, we aim to analyze the relationship between Klotho and inflammation. Vascular samples were obtained from 27 patients with atherosclerotic disease under an elective vascular surgery procedure, and from 11 control subjects (cadaveric organ donation programme). qRT-PCR was performed to analyze the gene expression of KLOTHO, TNF-α, IL-6 , and IL-10 Serum levels of soluble KLOTHO were measured by ELISA. As compared with control subjects, serum concentrations and vascular expression of Klotho were lower in patients with atherosclerotic vascular disease, whereas inflammatory status was significantly higher. There was a negative and significant correlation between inflammatory parameters and Klotho. After controlling for the effect of other variables, partial correlation showed a direct relationship between vascular KLOTHO gene expression and IL-10 mRNA levels, whereas there was a negative association with serum LDL concentrations and vascular TNF-α expression. Our study indicates an inverse interrelationship between inflammation and Klotho in atherosclerosis. Further studies are necessary to elucidate whether the inflammatory state causes Klotho deficiency or, on the contrary, reduction of Klotho could be responsible for greater inflammation, and finally, to investigate the potential clinical relevance of this association.<br /> (© 2017 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society.)
- Subjects :
- Female
Fibroblast Growth Factors genetics
Fibroblast Growth Factors metabolism
Glucuronidase deficiency
Glucuronidase genetics
Humans
Inflammation genetics
Interleukin-10 blood
Klotho Proteins
Male
Renal Insufficiency, Chronic blood
Solubility
Tumor Necrosis Factor-alpha blood
Atherosclerosis genetics
Atherosclerosis metabolism
Gene Expression physiology
Glucuronidase metabolism
Inflammation metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1470-8736
- Volume :
- 131
- Issue :
- 21
- Database :
- MEDLINE
- Journal :
- Clinical science (London, England : 1979)
- Publication Type :
- Academic Journal
- Accession number :
- 28963437
- Full Text :
- https://doi.org/10.1042/CS20171242