Literature DB >> 11451755

Distribution of lipid deposits around aortic branches of mice lacking LDL receptors and apolipoprotein E.

C J McGillicuddy1, M J Carrier, P D Weinberg.   

Abstract

Mice with inactivated genes are increasingly used as models of human atherosclerosis. The aim of the present study was to determine whether the characteristic age-related distributions of lipid deposition seen around human arterial branches are replicated in such mice. Lesions occur downstream of branch ostia in immature human aortas, but these regions are spared in adult vessels, with lesions occurring more frequently at the sides or upstream of the branches. We determined the pattern of lipid staining around 102 intercostal branch ostia from apolipoprotein E/low density lipoprotein receptor double-knockout mice aged 9 to 20 weeks by using en face microscopy and a frequency-mapping technique. Lesion prevalence was high in the ostium and the region immediately surrounding it. Frequencies were 2.12+/-0.30 (mean+/-SEM, n=11) times higher upstream than downstream (P<0.01), but the pattern did not resemble the adult human pattern: there were no peaks in frequency at the sides or upstream of the branch, and there was no sparing downstream. Furthermore, a patch of sparing upstream of the branch was seen, which has not been reported for human vessels, and there was no trend toward a more upstream pattern with age. We conclude that knockout mice may not be a suitable model in which to investigate localizing factors.

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Year:  2001        PMID: 11451755     DOI: 10.1161/hq0701.091996

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  8 in total

1.  Study of the development of the mouse thoracic aorta three-dimensional macromolecular structure using two-photon microscopy.

Authors:  Leah M Zadrozny; Edward B Neufeld; Bertrand M Lucotte; Patricia S Connelly; Zu-Xi Yu; Lam Dao; Li-Yueh Hsu; Robert S Balaban
Journal:  J Histochem Cytochem       Date:  2014-10-31       Impact factor: 2.479

2.  Effect of Reynolds number and flow division on patterns of haemodynamic wall shear stress near branch points in the descending thoracic aorta.

Authors:  A Kazakidi; S J Sherwin; P D Weinberg
Journal:  J R Soc Interface       Date:  2008-09-23       Impact factor: 4.118

Review 3.  S1P in the development of atherosclerosis: roles of hemodynamic wall shear stress and endothelial permeability.

Authors:  Christina M Warboys; Peter D Weinberg
Journal:  Tissue Barriers       Date:  2021-09-18

4.  Intimal cushions and endothelial nuclear elongation around mouse aortic branches and their spatial correspondence with patterns of lipid deposition.

Authors:  Andrew R Bond; Chih-Wen Ni; Hanjoong Jo; Peter D Weinberg
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-11-20       Impact factor: 4.733

Review 5.  Haemodynamic Wall Shear Stress, Endothelial Permeability and Atherosclerosis-A Triad of Controversy.

Authors:  Peter D Weinberg
Journal:  Front Bioeng Biotechnol       Date:  2022-03-07

Review 6.  Does low and oscillatory wall shear stress correlate spatially with early atherosclerosis? A systematic review.

Authors:  Veronique Peiffer; Spencer J Sherwin; Peter D Weinberg
Journal:  Cardiovasc Res       Date:  2013-03-03       Impact factor: 10.787

7.  γδT cells are prevalent in the proximal aorta and drive nascent atherosclerotic lesion progression and neutrophilia in hypercholesterolemic mice.

Authors:  Duc M Vu; Albert Tai; Jeffrey B Tatro; Richard H Karas; Brigitte T Huber; Debbie Beasley
Journal:  PLoS One       Date:  2014-10-14       Impact factor: 3.240

8.  Role of endothelial permeability hotspots and endothelial mitosis in determining age-related patterns of macromolecule uptake by the rabbit aortic wall near branch points.

Authors:  K Yean Chooi; Andrew Comerford; Stephanie J Cremers; Peter D Weinberg
Journal:  Atherosclerosis       Date:  2016-05-07       Impact factor: 5.162

  8 in total

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