Inflammation: a culprit for vascular calcification in atherosclerosis and diabetes

被引:182
作者
Bessueille, L. [1 ]
Magne, D. [1 ]
机构
[1] Univ Lyon, ICBMS UMR CNRS 5246, F-69622 Villeurbanne, France
关键词
Vascular smooth muscle cells; Chondrocytes; TNF-alpha; IL-1; beta; Inflammasome; SMOOTH-MUSCLE-CELLS; NECROSIS-FACTOR-ALPHA; CORONARY-ARTERY CALCIUM; HUTCHINSON-GILFORD-PROGERIA; C-REACTIVE PROTEIN; E-KNOCKOUT MICE; CARDIOVASCULAR RISK-FACTORS; BEAM COMPUTED-TOMOGRAPHY; BONE-MINERAL DENSITY; APOE-DEFICIENT MICE;
D O I
10.1007/s00018-015-1876-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
It is today acknowledged that aging is associated with a low-grade chronic inflammatory status, and that inflammation exacerbates age-related diseases such as osteoporosis, Alzheimer's disease, atherosclerosis and type 2 diabetes mellitus (T2DM). Vascular calcification is a complication that also occurs during aging, in particular in association with atherosclerosis and T2DM. Recent studies provided compelling evidence that vascular calcification is associated with inflammatory status and is enhanced by inflammatory cytokines. In the present review, we propose on one hand to highlight the most important and recent findings on the cellular and molecular mechanisms of vascular inflammation in atherosclerosis and T2DM. On the other hand, we will present the effects of inflammatory mediators on the trans-differentiation of vascular smooth muscle cell and on the deposition of crystals. Since vascular calcification significantly impacts morbidity and mortality in affected individuals, a better understanding of its induction and development will pave the way to develop new therapeutic strategies.
引用
收藏
页码:2475 / 2489
页数:15
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