Proteomic profiling in apolipoprotein E-deficient mice during atherosclerosis progression

Dursun E., ÖZBEN SADIÇ B., Monari E., Cuoghi A., Tomasi A., Ozben T.

ACTA HISTOCHEMICA, vol.112, no.2, pp.178-188, 2010 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 112 Issue: 2
  • Publication Date: 2010
  • Doi Number: 10.1016/j.acthis.2008.10.007
  • Journal Name: ACTA HISTOCHEMICA
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.178-188
  • Keywords: Atherosclerosis, Apolipoprotein E-deficient mice, Proteomics, SELDI-TOF-MS, E-O MICE, OXIDATIVE STRESS, POLYPHENOLS, LESION
  • Akdeniz University Affiliated: Yes

Abstract

Atherosclerosis and related complications are a major worldwide cause of human morbidity and mortality. It is advantageous to perform atherosclerosis studies in the apolipoprotein E-deficient (Apo E-/-) mouse model, which develops atherosclerosis very fast in comparison to humans. The aim of this study was to compare serum protein profiles in Apo E-/- mice during atherosclerosis progression with the data of control C57BL/6 mice. Serum proteomic analyses were performed using surface-enhanced laser desorption/ionization-time of flight mass spectrometry (SELDI-TOF-MS). The protein profiles obtained using three different chips, CM-10 (weak cation exchange), H50 (reversed-phase) and IMAC-30 (immobilized metal affinity capture) were statistically analyzed using the ProteinChip data manager 3.0 program. At 20 weeks of age, all Apo E-/- mice developed early atherosclerotic lesions. The peak intensities of 742 serum protein/peptide clusters were found to be different between the atherosclerotic and control mice groups, and the differences reached statistical significance for 107 serum protein/peptide clusters (p<0.05). This study contributes to understanding the changes in serum protein/peptide profiles during atherosclerosis development and may inform discovery of new protein biomarkers for early diagnosis of atherosclerosis. (C) 2008 Elsevier GmbH. All rights reserved.