作者: Hiroko Hanzawa , Takeshi Sakamoto , Akihito Kaneko , Naomi Manri , Yan Zhao
DOI: 10.1021/ACS.JPROTEOME.5B00405
关键词:
摘要: Atherogenic cardiovascular diseases are the major cause of mortality. Prevention and prediction incidents is important; however, biomarkers that directly reflect disease progression remain poorly investigated. To elucidate molecular determinants atherogenesis, proteomic approaches advantageous by using model animals for comparing changes occurring systematically (bloodstream) locally (lesion) in accordance with stages. We conducted differential mass spectrometric analysis between apolipoprotein E deficient (apoED) wild-type (wt) mice plasma arterial tissue both types obtained at four pathognomonic time points disease. A total 100 proteins 390 tissues were continuously detected throughout points; 29 identified common. Of those, 13 36 showed significant difference abundance apoED wt certain points. Importantly, we found quantitative variation patterns regarding did not always correspond tissues, resulting gaining insight into atherosclerotic plaque progression. These characteristic to be components inflammation, thrombus formation, vascular remodeling, suggesting drastic integrative alteration atherosclerosis development.