Flow shear stress affects macromolecular accumulation through modulation of internal elastic lamina fenestrae

Clinical Biomechanics

Volumn 23, Issue SUPLL.1, 2008, Pages

  Guo, Zi Yi ^a   Yan, Zhi Qiang ^a   Bai, Ling ^a   Zhang, Ming Liang ^a   Jiang, Zong Lai ^a  

^a SHANGHAI JIAO TONG UNIVERSITY   (China)

Author keywords

Atherogenesis; Fenestra; Internal elastic lamina; Remodeling; Shear stress

Indexed keywords

CONCENTRATION (PROCESS); CONFOCAL MICROSCOPY; ENDOTHELIAL CELLS; MACROMOLECULES; MICROSCOPIC EXAMINATION; MODULATION; MOLECULAR INTERACTIONS; PAINTING; STRENGTH OF MATERIALS; SUPRAMOLECULAR CHEMISTRY; WALLS (STRUCTURAL PARTITIONS);

ATHEROGENESIS; COMMON CAROTID ARTERIES; FENESTRA; INTERNAL ELASTIC LAMINA; REMODELING;

SHEAR STRESS;

FIBRONECTIN; HORSERADISH PEROXIDASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTERY WALL; ARTICLE; BOWMAN MEMBRANE; CAROTID ARTERY; CELL FUNCTION; COCHLEA FENESTRA; CONFOCAL MICROSCOPY; CORNEA; ENDOTHELIUM CELL; IMMUNOHISTOLOGY; INTERNAL ELASTIC LAMINA; MACROMOLECULE; MALE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; SHEAR STRESS; WESTERN BLOTTING;

ANIMALS; BLOOD FLOW VELOCITY; CAROTID ARTERIES; FIBRONECTINS; HORSERADISH PEROXIDASE; MALE; MECHANOTRANSDUCTION, CELLULAR; RATS; RATS, SPRAGUE-DAWLEY; SHEAR STRENGTH;

EID: 50349095139     PISSN: 02680033     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.clinbiomech.2007.08.017     Document Type: Article

References (22)

1. Bézie Y., Lamaziere J.M., Laurent S., Challande P., Cunha R.S., Bonnet J., and Lacolley P. Fibronectin expression and aortic wall elastic modulus in spontaneously hypertensive rats. Arterioscl. Thromb. Vasc. Biol. 18 (1998) 1027-1034
2. Boumaza S., Arribas S.M., Osborne-Pellegrin M., McGrath J.C., Laurent S., Lacolley P., and Challande P. Fenestrations of the carotid internal elastic lamina and structural adaptation in stroke-prone spontaneously hypertensive rats. Hypertension 37 (2001) 1101-1107
3. Campbell G.J., and Roach M.R. Fenestrations in the internal elastic lamina at bifurcations of human cerebral arteries. Stroke 12 (1981) 489-496
4. Cheng C., Tempel D., van Haperen R., van der Baan A., Grosveld F., Daemen M.J., Krams R., and de Crom R. Atherosclerotic lesion size and vulnerability are determined by patterns of fluid shear stress. Circulation 113 (2006) 2744-2753
5. Fry D.L. Mass transport, atherogenesis, and risk. Arteriosclerosis 7 (1987) 88-100
6. Huang Y., Rumschitzki D., Chien S., and Weinbaum S. A fiber matrix model for the filtration through fenestral pores in a compressible arterial intima. Am. J. Physiol. 272 (1997) H2023-H2039
7. Huang Y., Jan K.M., Rumschitzki D., and Weinbaum S. Structural changes in rat aortic intima due to transmural pressure. J. Biomech. Eng. 120 (1998) 476-483
8. Khan B.V., Parthasarathy S.S., Alexander R.W., and Medford R.M. Modified low density lipoprotein and its constituents augment cytokine-activated vascular cell adhesion molecule-1 gene expression in human vascular endothelial cells. J. Clin. Invest. 95 (1995) 1262-1270
9. Lanir Y. The possible role of intimal convective transport in atherogenesis. Biorheology 21 (1984) 643-647
10. Laurent S., Boutouyrie P., and Lacolley P. Structural and genetic bases of arterial stiffness. Hypertension 45 (2005) 1050-1055
11. Lee K., Forudi F., Saidel G.M., and Penn M.S. Alterations in internal elastic lamina permeability as a function of age and anatomical site precede lesion development in apolipoprotein E-null mice. Circ. Res. 97 (2005) 450-456
12. Miyashiro J.K., Poppa V., and Berk B.C. Flow-induced vascular remodeling in the rat carotid artery diminishes with age. Circ. Res. 81 (1997) 311-319
13. Penn M.S., and Chisolm G.M. Relation between lipopolysaccharide-induced endothelial cell injury and entry of macromolecules into the rat aorta in vivo. Circ. Res. 68 (1991) 1259-1269
14. Schwenke D.C., and Carew T.E. Initiation of atherosclerotic lesions in cholesterol fed rabbits. II. Selective retention of LDL vs. selective increases in LDL permeability in susceptible sites of arteries arteriosclerosis. Arteriosclerosis 9 (1989) 908-918
15. Steinberg D., Parthasarathy S., Carew T.E., Khoo J.C., and Witztum J.L. Beyond cholesterol. Modifications of low-density lipoprotein that increase its atherogenicity. N. Engl. J. Med. 14 (1989) 915-924
16. Tada S., and Tarbell J.M. Internal elastic lamina affects the distribution of macromolecules in the arterial wall: a computational study. Am. J. Physiol. Heart Circ. Physiol. 287 (2004) H905-H913
17. Tarbell J.M. Mass transport in arteries and the localization of atherosclerosis. Ann. Rev. Biomed. Eng. 5 (2003) 79-118
18. Tohda K., Masuda H., Kawamura K., and Shozawa T. Difference in dilatation between endothelium-preserved and -desquamated segments in the flow-loaded rat common carotid artery. Arterioscl. Thromb. 12 (1992) 519-528
19. VanderLaan P.A., Reardon C.A., and Getz G.S. Site specificity of atherosclerosis: site-selective responses to atherosclerotic modulators. Arterioscl. Thromb. Vasc. Biol. 24 (2004) 12-22
20. van Hinsbergh W.M. Endothelial permeability for macromolecules. Mechanistic aspects of pathophysiological modulation. Arterioscl. Thromb. Vasc. Biol. 17 (1997) 1018-1023
21. Weinbaum S., Tzeghai G., Ganatos P., Pfeffer R., and Chien S. Effect of cell turnover and leaky junctions on arterial macromolecular transport. Am. J. Physiol. 248 (1985) H945-H960
22. Wong L.C., and Langille B.L. Developmental remodeling of the internal elastic lamina of rabbit arteries: effect of blood flow. Circ. Res. 78 (1996) 799-805