How radiation influences atherosclerotic plaque development: a biophysical approach in ApoE-/- mice

被引:6
作者
Kloosterman, Astrid [1 ]
van Dillen, Teun [1 ]
Bijwaard, Harmen [1 ,2 ]
Heeneman, Sylvia [3 ]
Hoving, Saske [4 ]
Stewart, Fiona A. [4 ]
Dekkers, Fieke [1 ]
机构
[1] Natl Inst Publ Hlth & Environm RIVM, Ctr Environm Safety & Secur, Bilthoven, Netherlands
[2] Inholland Univ Appl Sci, Med Technol Res Grp, Haarlem, Netherlands
[3] Maastricht Univ, Med Ctr, Expt Vasc Pathol Grp, Dept Pathol,Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands
[4] Antoni van Leeuwenhoek Hosp, Netherlands Canc Inst, Div Biol Stress Response H3, Amsterdam, Netherlands
关键词
Atherosclerosis; Mathematical modeling; ApoE(-/-) mice; Ionizing radiation; FOAM CELL-FORMATION; ENDOTHELIAL-CELLS; MONOCYTE; IRRADIATION; REGRESSION; MECHANISM; DISEASE; LESIONS; DAMAGE; HDL;
D O I
10.1007/s00411-017-0709-2
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Atherosclerosis is the development of lipid-laden plaques in arteries and is nowadays considered as an inflammatory disease. It has been shown that high doses of ionizing radiation, as used in radiotherapy, can increase the risk of development or progression of atherosclerosis. To elucidate the effects of radiation on atherosclerosis, we propose a mathematical model to describe radiation-promoted plaque development. This model distinguishes itself from other models by combining plaque initiation and plaque growth, and by incorporating information from biological experiments. It is based on two consecutive processes: a probabilistic dose-dependent plaque initiation process, followed by deterministic plaque growth. As a proof of principle, experimental plaque size data from carotid arteries from irradiated ApoE mice was used to illustrate how this model can provide insight into the underlying biological processes. This analysis supports the promoting role for radiation in plaque initiation, but the model can easily be extended to include dose-related effects on plaque growth if available experimental data would point in that direction. Moreover, the model could assist in designing future biological experiments on this research topic. Additional biological data such as plaque size data from chronically-irradiated mice or experimental data sets with a larger variety in biological parameters can help to further unravel the influence of radiation on plaque development. To the authors' knowledge, this is the first biophysical model that combines probabilistic and mechanistic modeling which uses experimental data to investigate the influence of radiation on plaque development.
引用
收藏
页码:423 / 431
页数:9
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