Integrative Physiology/Experimental Medicine |
From the Departments of Medicine (B.J.B., S.S.W., X.P.W., X.W., A.J.L.), Microbiology, Immunology, and Molecular Genetics (A.J.L.), and Human Genetics (A.J.L.), UCLA School of Medicine, University of California, Los Angeles.
Correspondence to Brian J. Bennett, Department of Medicine, 675 Charles E. Young Dr South, 3730 MRL, University of California at Los Angeles, Los Angeles, CA 90095-1679. E-mail bbennett{at}mednet.ucla.edu
Objective— We sought to determine the genetic factors contributing to atherosclerotic plaque size and cellular composition in the innominate artery, a murine model of advanced atherosclerosis.
Methods and Results— We examined genetic contributions to innominate atherosclerotic plaque size and cellular composition in an intercross between C57BL/6J.Apoe–/–, a strain susceptible to aortic lesions, and C3H/HeJ.Apoe–/–, a strain resistant to aortic lesions. Surprisingly, total innominate lesion size was similar in the two strains. Genetic analyses identified one novel locus on Chromosome 2 for innominate artery lesion size, a significant locus for fibrous cap thickness on Chromosome 15, and several suggestive loci for cellular composition, all distinct from loci influencing aortic lesions. The Chromosome 2 locus contains a candidate, CD44. We show that CD44 is expressed in the innominate artery and differs strikingly in expression between the parental strains.
Conclusion— Multiple aspects of innominate lesion composition are genetically determined, but in a manner largely independent of the genetic contributions to aortic lesions.
We sought to determine the genetic factors contributing to atherosclerotic plaque size and cellular composition in the innominate artery. We identified one novel locus on Chromosome 2 for innominate artery lesion size. Multiple aspects of innominate lesion composition are genetically determined, but in a manner independent of the aortic sinus.
Key Words: innominate artery QTL atherosclerosis plaque stability
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