Matrix Remodeling in Vascular Calcification Associated with Chronic Kidney Disease

被引:58
|
作者
Pai, Ashwini S. [1 ]
Giachelli, Cecilia M. [1 ]
机构
[1] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
来源
关键词
SMOOTH-MUSCLE-CELLS; ARTERIAL; ELASTIN; METALLOPROTEINASES; INHIBITION; TGF-BETA-1; PHOSPHATE; CKD;
D O I
10.1681/ASN.2010040349
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Vascular calcification is a major contributor to cardiovascular disease, a leading cause of death in patients with chronic kidney disease. Mechanistic studies highlight the importance of dysregulated mineral metabolism, vascular osteochondrogenic processes, apoptosis, and deficiencies in calcification inhibitors as potential mediators of calcification in renal disease. However, the contribution of the extracellular matrix in vascular calcification associated with chronic kidney disease is less understood. Here we examine evidence that suggests important roles for elastin and elastin-degrading enzymes as potential key regulators of calcification. Additional studies aimed at further understanding their role are critical for the design of therapeutic interventions.
引用
收藏
页码:1637 / 1640
页数:4
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