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AGE-Induced Suppression of EZH2 Mediates Injury of Podocytes by Reducing H3K27me3.
- Source :
-
American journal of nephrology [Am J Nephrol] 2020; Vol. 51 (9), pp. 676-692. Date of Electronic Publication: 2020 Aug 27. - Publication Year :
- 2020
-
Abstract
- Background: Chronic hyperglycemia, a pivotal feature of diabetes mellitus (DM), initiates the formation of advanced glycation end products (AGEs) and the dysregulation of epigenetic mechanisms, which may cause injury to renal podocytes, a central feature of diabetic kidney disease (DKD). Previous data of our group showed that AGEs significantly reduce the expression of NIPP1 (nuclear inhibitor of protein phosphatase 1) in podocytes in vitro as well as in human and murine DKD. NIPP1 was shown by others to interact with enhancer of zeste homolog 2 (EZH2), which catalyzes the repressive methylation of H3K27me3 on histone 3. Therefore, we hypothesized that AGEs can directly induce epigenetic changes in podocytes.<br />Methods: We analyzed the relevance of AGEs on EZH2 expression and activity in a murine podocyte cell line. Cells were treated with 5 mg/mL glycated BSA for 24 h. To determine the meaning of EZH2 suppression, EZH2 activity was inhibited by incubating the cells with the pharmacological methyltransferase inhibitor 3-deazaneplanocin A; EZH2 expression was repressed with siRNA. mRNA expression was analyzed with real-time PCR, and protein expression with Western blot. EZH2 expression and level of H3K27 trimethylation in podocytes of diabetic db/db mice, a mouse model for type 2 DM, were analyzed using immunofluorescence.<br />Results: Our data demonstrated that AGEs decrease EZH2 expression in podocytes and consequently reduce H3K27me3. This suppression of EZH2 mimicked the AGE effects and caused an upregulated expression of pathological factors that contribute to podocyte injury in DKD. In addition, analyses of db/db mice showed significantly reduced H3K27me3 and EZH2 expression in podocytes. Moreover, the suppression of NIPP1 and EZH2 showed similar effects regarding podocyte injury.<br />Conclusions: Our studies provide a novel pathway how AGEs contribute to podocyte injury and the formation of the so-called metabolic memory in DKD.<br /> (© 2020 S. Karger AG, Basel.)
- Subjects :
- Adenosine analogs & derivatives
Adenosine pharmacology
Animals
Cell Line
DNA Methylation drug effects
Diabetic Nephropathies pathology
Disease Models, Animal
Enhancer of Zeste Homolog 2 Protein antagonists & inhibitors
Epigenesis, Genetic drug effects
Humans
Intracellular Signaling Peptides and Proteins antagonists & inhibitors
Intracellular Signaling Peptides and Proteins genetics
Intracellular Signaling Peptides and Proteins metabolism
Mice
RNA, Small Interfering
Diabetic Nephropathies genetics
Enhancer of Zeste Homolog 2 Protein metabolism
Glycation End Products, Advanced metabolism
Podocytes pathology
Subjects
Details
- Language :
- English
- ISSN :
- 1421-9670
- Volume :
- 51
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- American journal of nephrology
- Publication Type :
- Academic Journal
- Accession number :
- 32854097
- Full Text :
- https://doi.org/10.1159/000510140