Systems Biology of Vascular Calcification

被引:10
作者
Sage, Andrew [1 ,2 ,3 ,4 ]
Tintut, Yin [1 ,2 ,3 ,4 ]
Garfinkel, Alan [1 ,2 ,3 ,4 ]
Demer, Linda [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Los Angeles, Dept Med Cardiol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Physiol Sci, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Physiol, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Bioengn, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院;
关键词
ADIPOGENIC DIFFERENTIATION; CELLS; BONE; PERICYTES; EXPRESSION; DISEASE; PROTEIN; ORGAN; FGF23;
D O I
10.1016/j.tcm.2009.07.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Vascular calcification, a prevalent and progressive disorder, involves numerous interactive, autocrine, paracrine, and endocrine regulatory mechanisms and is thus ideally suited for analysis using a systems approach. This approach focuses on creating quantitative, testable models of complex biological systems that take into consideration the time dimension. They are usually expressed as mathematical models, and because of their time dependence and complexity, they usually require computer stimulation to determine predicted outcomes. Here, we provide an example of such a model used to analyze self-organization and mineralization of vascular stent cells, using partial differential equations capable of accurately predicting experimental outcomes. Such systems-based models are useful in many aspects of cardiovascular medicine. (Trends Cardiovasc Med 2009; 19:118-123) (C) 2009, Elsevier Inc.
引用
收藏
页码:118 / 123
页数:6
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