4.7 Article

Circulating uromodulin inhibits vascular calcification by interfering with pro-inflammatory cytokine signalling

期刊

CARDIOVASCULAR RESEARCH
卷 117, 期 3, 页码 930-941

出版社

OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvaa081

关键词

Uromodulin; Vascular smooth muscle cells; Vascular calcification; Phosphate; Osteo-/chondrogenic transdifferentiation

资金

  1. Else Kroner-Fresenius-Stiftung [2017_A32]
  2. Berlin Institute of Health (BIH)
  3. Deutsche Forschungsgemeinschaft [AL2054/1-1, VO2259/2-1]
  4. DZHK (German Centre for Cardiovascular Research)
  5. European Union Seventh Framework Programme [FP7/2007-2013-603288-SysVasc]
  6. Fresenius Medical Care (Bad Homburg, Germany)
  7. Bundesministerium fur Bildung und Forschung
  8. Sonnenfeld-foundation
  9. Kuratorium fur Heimdialyse und Nierentransplantation e.V.-Stiftung Praventivmedizin

向作者/读者索取更多资源

The study found that uromodulin can reduce vascular calcification in CKD patients, possibly by interfering with cytokine-dependent pro-calcific signaling pathways. In CKD, decreased levels and carbamylation of uromodulin may contribute to vascular pathology.
Aims Uromodulin is produced exclusively in the kidney and secreted into both urine and blood. Serum levels of uromodulin are correlated with kidney function and reduced in chronic kidney disease (CKD) patients, but physiological functions of serum uromodulin are still elusive. This study investigated the role of uromodulin in medial vascular calcification, a key factor associated with cardiovascular events and mortality in CKD patients. Methods and results Experiments were performed in primary human (HAoSMCs) and mouse (MOVAS) aortic smooth muscle cells, cholecalciferol overload and subtotal nephrectomy mouse models and serum from CKD patients. In three independent cohorts of CKD patients, serum uromodulin concentrations were inversely correlated with serum calcification propensity. Uromodulin supplementation reduced phosphate-induced osteo-/chondrogenic transdifferentiation and calcification of HAoSMCs. In human serum, pro-inflammatory cytokines tumour necrosis factor alpha (TNF alpha) and inter-leukin-1 beta (IL-1 beta) co-immunoprecipitated with uromodulin. Uromodulin inhibited TNF alpha and IL-1 beta-induced osteo-/chondrogenic signalling and activation of the transcription factor nuclear factor kappa-light-chain-enhancer of activated beta cells (NF-kB) as well as phosphate-induced NF-kB-dependent transcriptional activity in HAoSMCs. In vivo, adeno-associated virus (AAV)-mediated overexpression of uromodulin ameliorated vascular calcification in mice with cholecalciferol overload. Conversely, cholecalciferol overload-induced vascular calcification was aggravated in uromodulin-deficient mice. In contrast, uromodulin overexpression failed to reduce vascular calcification during renal failure in mice. Carbamylated uromodulin was detected in serum of CKD patients and uromodulin carbamylation inhibited its anti-calcific properties in vitro. Conclusions Uromodulin counteracts vascular osteo-/chondrogenic transdifferentiation and calcification, at least in part, through interference with cytokine-dependent pro-calcific signalling. In CKD, reduction and carbamylation of uromodulin may contribute to vascular pathology. [GRAPHICS] .

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据