Cdon suppresses vascular smooth muscle calcification via repression of the Wnt/Runx2 Axis

© 2023. The Author(s)..

Osteogenic transdifferentiation of vascular smooth muscle cells (VSMCs) is a risk factor associated with vascular diseases. Wnt signaling is one of the major mechanisms implicated in the osteogenic conversion of VSMCs. Since Cdon has a negative effect on Wnt signaling in distinct cellular processes, we sought to investigate the role of Cdon in vascular calcification. The expression of Cdon was significantly downregulated in VSMCs of the aortas of patients with atherosclerosis and aortic stenosis. Consistently, calcification models, including vitamin D3 (VD3)-injected mice and VSMCs cultured with calcifying media, exhibited reduced Cdon expression. Cdon ablation mice (cKO) exhibited exacerbated aortic stiffness and calcification in response to VD3 compared to the controls. Cdon depletion induced the osteogenic conversion of VSMCs accompanied by cellular senescence. The Cdon-deficient aortas showed a significant alteration in gene expression related to cell proliferation and differentiation together with Wnt signaling regulators. Consistently, Cdon depletion or overexpression in VSMCs elevated or attenuated Wnt-reporter activities, respectively. The deletion mutant of the second immunoglobulin domain (Ig2) in the Cdon ectodomain failed to suppress Wnt signaling and osteogenic conversion of VSMCs. Furthermore, treatment with purified recombinant proteins of the entire ectodomain or Ig2 domain of Cdon displayed suppressive effects on Wnt signaling and VSMC calcification. Our results demonstrate a protective role of Cdon in VSMC calcification by suppressing Wnt signaling. The Ig2 domain of Cdon has the potential as a therapeutic tool to prevent vascular calcification.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:55

Enthalten in:

Experimental & molecular medicine - 55(2023), 1 vom: 07. Jan., Seite 120-131

Sprache:

Englisch

Beteiligte Personen:

Ahn, Byeong-Yun [VerfasserIn]
Jeong, Yideul [VerfasserIn]
Kim, Sunghee [VerfasserIn]
Zhang, Yan [VerfasserIn]
Kim, Su Woo [VerfasserIn]
Leem, Young-Eun [VerfasserIn]
Kang, Jong-Sun [VerfasserIn]

Links:

Volltext

Themen:

CDON protein, human
Cdon protein, mouse
Cell Adhesion Molecules
Core Binding Factor Alpha 1 Subunit
Journal Article
Research Support, Non-U.S. Gov't
Runx2 protein, mouse

Anmerkungen:

Date Completed 25.02.2023

Date Revised 25.02.2023

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1038/s12276-022-00909-7

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM35120699X