Literature DB >> 34918390

NRF2-suppressed vascular calcification by regulating the antioxidant pathway in chronic kidney disease.

Donghua Jin1, Lihua Lin1, Yuxian Xie1, Miao Jia1, Hong Qiu1, Kang Xun1.   

Abstract

Vascular calcification (VC), in which vascular smooth muscle cells (VSMCs) undergo differentiation and osteogenic transition, is a common complication of chronic kidney disease (CKD). Recent findings show that nuclear factor-erythroid-2-related factor 2 (NRF2) is an evolutionarily conserved antioxidant and beneficial in preventing vascular senescence and calcification. The roles of NRF2 in the initiation and progression of VC in CKD still need further investigation. CKD-associated VC model rats exhibited significant upregulation of NRF2, NAD(P)H: quinone oxidoreductase-1 (NQO1), osteogenic markers such as alkaline phosphatase (ALP), runt-related transcription factor-2 (RUNX2) and osteopontin (OPN), and β-catenin compared to CKD rats. Immunohistochemistry further verified these results. In addition, rat aortic VSMCs were isolated and subjected to four treatments: normal control, phosphorus-induced (Pi), Pi + NRF2 activator DMF, and Pi + NRF2 inhibitor ML385. The reactive oxygen species (ROS) generation, malondialdehyde (MDA) content, and calcium deposition of the four treatments were determined. The mRNA and protein expression levels of NRF2, NQO1, and haem oxygenase 1 (HO1) and the osteogenic markers ALP, Runx1, OPN, bone morphogenetic protein 2 (BMP2), and β-catenin were quantified by RT-PCR and western blotting. VSMC apoptosis was calculated by flow cytometry. The in vitro results suggested that intracellular oxidative stress and calcification were closely associated with NRF2 activity and that the activation of NRF2 could significantly suppress osteogenic transition and apoptosis in VSMCs. Thus, this study indicated that the NRF2-related antioxidant pathway can positively respond to and protect against the initiation and progression of VC in CKD by reducing oxidative stress. This study may contribute insights facilitating the application of the NRF2 antioxidative system as a therapeutic treatment for vascular diseases such as CKD.
© 2021 Federation of American Societies for Experimental Biology.

Entities:  

Keywords:  NRF2; antioxidant pathway; chronic kidney disease; vascular calcification

Mesh:

Substances:

Year:  2022        PMID: 34918390     DOI: 10.1096/fj.202100625RR

Source DB:  PubMed          Journal:  FASEB J        ISSN: 0892-6638            Impact factor:   5.191


  5 in total

1.  Activation of Nrf2/HO-1 Antioxidant Pathway by Heme Attenuates Calcification of Human Lens Epithelial Cells.

Authors:  Arpan Chowdhury; Enikő Balogh; Haneen Ababneh; Andrea Tóth; Viktória Jeney
Journal:  Pharmaceuticals (Basel)       Date:  2022-04-19

Review 2.  The Role of Sirtuins in Osteogenic Differentiation of Vascular Smooth Muscle Cells and Vascular Calcification.

Authors:  Shuangshuang Wang; Siwang Hu
Journal:  Front Cardiovasc Med       Date:  2022-06-01

Review 3.  New Therapeutics Targeting Arterial Media Calcification: Friend or Foe for Bone Mineralization?

Authors:  Astrid Van den Branden; Anja Verhulst; Patrick C D'Haese; Britt Opdebeeck
Journal:  Metabolites       Date:  2022-04-05

Review 4.  Nrf2-Mediated Dichotomy in the Vascular System: Mechanistic and Therapeutic Perspective.

Authors:  Weiwei Wu; Andrew Hendrix; Sharad Nair; Taixing Cui
Journal:  Cells       Date:  2022-09-28       Impact factor: 7.666

Review 5.  Flow-Responsive Noncoding RNAs in the Vascular System: Basic Mechanisms for the Clinician.

Authors:  Salvatore De Rosa; Claudio Iaconetti; Ceren Eyileten; Masakazu Yasuda; Michele Albanese; Alberto Polimeni; Jolanda Sabatino; Sabato Sorrentino; Marek Postula; Ciro Indolfi
Journal:  J Clin Med       Date:  2022-01-17       Impact factor: 4.241

  5 in total

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