OBJECTIVE: Different strains of inbred mice exhibit different susceptibility to the development of atherosclerosis. The C3H/HeJ and C57Bl/6 mice have been used in several studies aimed at understanding the genetic basis of atherosclerosis. Under controlled environmental conditions, variations in susceptibility to atherosclerosis reflect differences in genetic makeup, and these differences must be reflected in gene expression patterns that are temporally related to the development of disease. In this study, we sought to identify the genetic pathways that are differentially activated in the aortas of these mice. METHODS AND RESULTS: We performed genome-wide transcriptional profiling of aortas from C3H/HeJ and C57Bl/6 mice. Differences in gene expression were identified at baseline as well as during normal aging and longitudinal exposure to high-fat diet. The significance of these genes to the development of atherosclerosis was evaluated by observing their temporal pattern of expression in the well-studied apolipoprotein E model of atherosclerosis. CONCLUSIONS: Gene expression differences between the 2 strains suggest that aortas of C57Bl/6 mice have a higher genetic propensity to develop inflammation in response to appropriate atherogenic stimuli. This study expands the repertoire of factors in known disease-related signaling pathways and identifies novel candidate genes for future study. To gain insights into the molecular pathways that are differentially activated in strains of mice with varied susceptibility to atherosclerosis, we performed comprehensive transcriptional profiling of their vascular wall. Genes identified through these studies expand the repertoire of factors in disease-related signaling pathways and identify novel candidate genes in atherosclerosis.
OBJECTIVE: Different strains of inbred mice exhibit different susceptibility to the development of atherosclerosis. The C3H/HeJ and C57Bl/6 mice have been used in several studies aimed at understanding the genetic basis of atherosclerosis. Under controlled environmental conditions, variations in susceptibility to atherosclerosis reflect differences in genetic makeup, and these differences must be reflected in gene expression patterns that are temporally related to the development of disease. In this study, we sought to identify the genetic pathways that are differentially activated in the aortas of these mice. METHODS AND RESULTS: We performed genome-wide transcriptional profiling of aortas from C3H/HeJ and C57Bl/6 mice. Differences in gene expression were identified at baseline as well as during normal aging and longitudinal exposure to high-fat diet. The significance of these genes to the development of atherosclerosis was evaluated by observing their temporal pattern of expression in the well-studied apolipoprotein E model of atherosclerosis. CONCLUSIONS: Gene expression differences between the 2 strains suggest that aortas of C57Bl/6 mice have a higher genetic propensity to develop inflammation in response to appropriate atherogenic stimuli. This study expands the repertoire of factors in known disease-related signaling pathways and identifies novel candidate genes for future study. To gain insights into the molecular pathways that are differentially activated in strains of mice with varied susceptibility to atherosclerosis, we performed comprehensive transcriptional profiling of their vascular wall. Genes identified through these studies expand the repertoire of factors in disease-related signaling pathways and identify novel candidate genes in atherosclerosis.
Authors: Joanna S Kerley-Hamilton; Heidi W Trask; Christian J A Ridley; Eric Dufour; Corina Lesseur; Carol S Ringelberg; Karen L Moodie; Samantha L Shipman; Murray Korc; Jiang Gui; Nicholas W Shworak; Craig R Tomlinson Journal: Toxicol Sci Date: 2012-01-06 Impact factor: 4.849
Authors: Solida Mak; Hua Sun; Frances Acevedo; Lawrence C Shimmin; Lei Zhao; Ba-Bie Teng; James E Hixson Journal: Atherosclerosis Date: 2010-07-07 Impact factor: 5.162
Authors: Hyung J Chun; Ziad A Ali; Yoko Kojima; Ramendra K Kundu; Ahmad Y Sheikh; Rani Agrawal; Lixin Zheng; Nicholas J Leeper; Nathan E Pearl; Andrew J Patterson; Joshua P Anderson; Philip S Tsao; Michael J Lenardo; Euan A Ashley; Thomas Quertermous Journal: J Clin Invest Date: 2008-10 Impact factor: 14.808
Authors: Themistocles L Assimes; Joshua W Knowles; James R Priest; Analabha Basu; Kelly A Volcik; Audrey Southwick; Holly K Tabor; Jaana Hartiala; Hooman Allayee; Megan L Grove; Raymond Tabibiazar; Stephen Sidney; Stephen P Fortmann; Alan Go; Mark Hlatky; Carlos Iribarren; Eric Boerwinkle; Richard Myers; Neil Risch; Thomas Quertermous Journal: Hum Genet Date: 2008-03-28 Impact factor: 4.132
Authors: Zuobiao Yuan; Toru Miyoshi; Yongde Bao; Jason P Sheehan; Alan H Matsumoto; Weibin Shi Journal: Am J Physiol Heart Circ Physiol Date: 2009-03-20 Impact factor: 4.733