| Literature DB >> 36229526 |
Rie Jo1,2, Hirotaka Shibata3,4, Isao Kurihara1,5, Kenichi Yokota1,6, Sakiko Kobayashi1, Ayano Murai-Takeda1,7, Yuko Mitsuishi1,8, Takeshi Hayashi1,9, Toshifumi Nakamura1, Hiroshi Itoh1.
Abstract
This study investigated the mechanism underlying the beneficial effects of mineralocorticoid receptor (MR) antagonists in patients with resistant hypertension and diabetic nephropathy by examining post-translational modification of the MR by O-linked-N-acetylglucosamine (O-GlcNAc), which is strongly associated with type 2 diabetes. Coimmunoprecipitation assays in HEK293T cells showed that MR is a target of O-GlcNAc modification (O-GlcNAcylation). The expression levels and transcriptional activities of the receptor increased in parallel with its O-GlcNAcylation under high-glucose conditions. Liquid chromatography-tandem mass spectrometry revealed O-GlcNAcylation of the MR at amino acids 295-307. Point mutations in those residues decreased O-GlcNAcylation, and both the protein levels and transcriptional activities of MR. In db/db mouse kidneys, MR protein levels increased in parallel with overall O-GlcNAc levels of the tissue, accompanied by increased SGK1 mRNA levels. The administration of 6-diazo-5-oxo-L-norleucin, an inhibitor of O-GlcNAcylation, reduced tissue O-GlcNAc levels and MR protein levels in db/db mice. Thus, our study showed that O-GlcNAcylation of the MR directly increases protein levels and transcriptional activities of the receptor under high-glucose conditions in vitro and in vivo. These findings provide a novel mechanism of MR as a target for prevention of complications associated with diabetes mellitus.Entities:
Keywords: Diabetes mellitus; Diabetic nephropathy; Hypertension; Mineralocorticoid receptor; O-linked N-acetylglucosamine
Year: 2022 PMID: 36229526 DOI: 10.1038/s41440-022-01036-6
Source DB: PubMed Journal: Hypertens Res ISSN: 0916-9636 Impact factor: 5.528