Aortic Valve
http://www.100md.com
《动脉硬化血栓血管生物学》
From the Institute for Medicine and Engineering (P.F.D., A.G.P., C.A.S.), and the Departments of Pathology and Laboratory Medicine (P.F.D.) and Bioengineering (P.F.D., A.G.P., C.A.S.), University of Pennsylvania, Philadelphia, Penn.
Aortic valve diseases are debilitating cardiovascular disorders associated with significant morbidity and mortality. Although there continue to be major efforts to improve the longevity of replacement valves and to improve tissue engineered substitutes,1 the underlying mechanisms that may be responsible for the initiation and development of valve pathology have received less attention than have other sclerosing cardiovascular diseases such as atherogenesis. The endothelium lining of the cardiovascular system plays an important regulatory role in vascular physiology and pathology. In similar fashion, the surfaces of valve leaflets are presumed to be generally protected (eg, anticoagulant) and regulated (eg, permeability) by the endothelium. The functional properties of endothelium or its presence/absence are associated with a variety of valve pathologies,2 and systemic endothelial dysfunction is linked to aortic valve calcification.3 However, only recently have cell and molecular studies focused on the characterization of valve endothelial phenotypes with the idea that some aspects of phenotypic change or dysfunction may contribute to valve pathologies, a situation analogous to atherogenesis.
See page 1429
During the cardiac cycle, the aortic valve endothelium is subjected to complex fluid dynamics that are distinctly different on each side of the valve. As has been described for many years, arterial endothelial alignment in vivo generally follows the measured or predicted shear stress direction,4 and endothelial cells in vitro align with the dominant direction of the applied shear stress.5 The responses, which are reversible,4,6 represent endothelial structural remodeling in response to hemodynamic shear stress. It might be expected that endothelial cells isolated from aortic valves and grown in tissue culture will behave in a similar manner as arterial endothelium. However, in this issue of Arteriosclerosis, Thrombosis, and Vascular Biology, Butcher et al7 demonstrate that aortic valve endothelium in culture exhibits a distinctly different response to directional flow than that shown by cultured arterial endothelium isolated from nearby regions of the aorta. The study was inspired by the observations made by Deck et al8 that endothelium on the ventricular aortic valve surface tends to align circumferentially with the free edge of the leaflets rather than in the direction of predicted maximum shear stress induced by systolic flow. The new studies show that over a 48 hour period, cultured aortic valve endothelial cells align perpendicular to, rather than parallel to, the flow direction. The alignment differences were associated with differences in signaling pathways. Although arterial endothelial cell alignment was dependent on both Rho-kinase and phosphatidylinositol 3-kinase (PI3K) pathways, valve endothelium appeared not to require activation of PI3K to align perpendicular to the flow. These findings are relevant to valve pathology and to the development of replacement tissues, as well as to the broader issues of endothelial phenotypic heterogeneity (Figure).
Endothelial heterogeneity scaled for valve vs artery, aortic side vs ventricular side of the aortic valve, and cell-to-cell variation within the monolayer of each side.
In normal mammals, endothelial phenotype appears to be determined by a combination of intrinsic programmed gene expression9 and local epigenetic or environmental factors. Of the latter, the influence of the local hemodynamic environment on phenotype in vitro10,11 and in vivo12,13 has clearly been demonstrated. Endothelial orientation is also subject to "contact guidance" by the underlying substrate in situ.14 Contact guidance is consistent with the physical continuity of extracellular matrix (ECM), focal adhesions, and cytoskeletal elements, connections that are important in the determination of cell morphology and cell differentiation. Cytoskeletal organization and focal adhesion biology are highly regulated by Rho-kinase and PI3K signaling pathways,15 which were noted to be different for valve versus arterial endothelium.7 Some memory of orientation may have been carried over to the cultured valve endothelial cells to direct the synthesis of oriented ECM in the experiments conducted by Butcher et al. However, if this were the case, the valve cells required the reintroduction of flow to activate such memory. Whatever the explanations for the valve cell alignment responses, the study demonstrates interesting phenotypic differences for cultured valve endothelium that have implications for endothelial biology in general as well as for cell source considerations and engineered phenotypes for tissue engineered valve substitutes. The useful applications of this finding, however, will best be realized by investigating differential endothelial phenotypes in greater detail and at improved spatial resolution within the valve structure itself (see below).
Global endothelial gene expression analysis is a powerful tool to investigate spatial heterogeneity of endothelial phenotypes in general. Farivar et al16 noted significant differences in transcriptionally active genes expressed by arterial and valve endothelial cells grown in primary culture. Although there was common expression of 55 activated genes (of 847 interrogated), an additional 48 active genes were expressed by only one or the other cell type. Phenotypic memory in culture was also recently noted by Chi et al9 in endothelial cells isolated from many different vascular locations and then cultured for up to 5 passages before transcriptional profiling. Remarkably, hierarchical clustering revealed patterns of gene expression that reflected some of the known properties of the cells in situ; arterial versus venous markers, microvascular characteristics, and even characteristics of vascular bed symmetry were identified. Intrinsic differential phenotypic properties of endothelium therefore appear to be established during development, then presumably reinforced, enhanced, and retained by cues present in the local environment. The extent to which the intrinsic differentiated phenotype is further regulated by local conditions, such as hemodynamic/biomechanical stimuli, can now be investigated globally at the level of gene expression and in a more limited way for candidate protein expression and activity.
Refinements of genomics techniques permit transcriptional profiling of small regions of endothelium reflective of the steady state in vivo.17 This has recently been used to address regional phenotypic differences as a function of hemodynamic characteristics in both arteries13 and heart valves.18 Passerini et al13 profiled endothelial cells isolated directly from arterial regions of disturbed and undisturbed flow in normal adult pigs to better define gene expression changes that underlie a predisposition to atherogenesis in regions of complex blood flow. The coexistence of pro- and antiinflammatory gene expression patterns in the same athero-susceptible locations was noted. This balance of opposing mechanisms suggests that endothelial cells were primed for an atherogenic inflammatory response but kept in check by compensatory mechanisms in the absence of additional risk factors. The studies identified arterial hemodynamics as a contributor to regional endothelial heterogeneity via multiple pathways and as a subtle risk factor for athero-susceptibility. A similar approach is currently being applied to differential phenotyping of heart valve endothelium.18 In this emerging work, the principal objective is to refine the spatial genomics to comparisons of each side of the valve leaflet because differential susceptibility to calcific sclerosis is side-specific.19 Calcification occurs preferentially in the aortic valve on the side that is exposed to more highly disturbed blood flow, suggestive of a role for hemodynamics in valvular calcification. Thus there are hemodynamic similarities to the disturbed flow characteristics that spatially correlate with regions of athero-susceptibility in large arteries.13,20 In paired comparisons of aortic side versus ventricular side endothelium, Simmons et al (manuscript in preparation) observed differential transcriptional profiles across multiple pathways, including prominent representation of proliferative, apoptotic, and calcification pathways. These early data suggest differential endothelial phenotypes that define the sidedness of the aortic valve, a significant improvement in spatial resolution for this tissue (Figure, middle). The approach also addresses the complex mechanisms associated with aortic-side susceptibility of the valve to sclerosis and calcification. Furthermore, it should be possible to contrast the in situ and intrinsic (cultured) phenotypes, because valve endothelium from each side can be cultured for comparison of gene expression profiles from the same tissues in vitro and in situ. A higher level of spatial resolution would be obtained by profiling single or small groupings of endothelial cells.21 There is ample evidence of cell-to-cell heterogeneity of endothelial morphology22 and transport properties23 throughout the aortic valve suggesting that phenotypic differences might be resolved at the single cell level (Figure, right).
In summary, the provocative observations noted by Butcher et al in culture reveal interesting differences in the responses to flow of the valve endothelium compared with the aortic endothelium. However, they likely represent merely the tip of the iceberg regarding valve endothelial phenotypes, and in situ endothelial heterogeneity in general.8,20 More detailed investigation of both valve and vascular bed endothelium is required by global phenotyping at the highest spatial resolution possible.
Vascular phenotyping research in the Davies laboratory is supported by National Institutes of Health (National Heart, Lung, and Blood Institute) grants HL36049 (MERIT), HL64388, and HL62250, National Aeronautics and Space Administration-National Space Biomedical Research Institute grant 01-102, National Institutes of Health Training grant HL07954 (to A.G.P.), and American Heart Association Postdoctoral Fellowship 0325666U (to C.A.S.).
References
Schoen FJ, Levy RJ. Tissue heart valves: current challenges and future research perspectives. J Biomed Mater Res. 1999; 47: 439–465.
Muller AM, Cronen C, Kupferwasser LI, Oelert H, Muller KM, Kirkpatrick CJ. Expression of endothelial cell adhesion molecules on heart valves: up-regulation in degeneration as well as acute endocarditis. J Pathol. 2000; 191: 54–60.
Poggianti E, Venneri L, Chubuchny V, Jambrik Z, Baroncini LA, Picano E. Aortic valve sclerosis is associated with systemic endothelial dysfunction. J Am Coll Cardiol. 2003; 41: 136–141.
Flaherty JT, Pierce JE, Ferrans VJ, Patel DJ, Tucker WK, Fry DL. Endothelial nuclear patterns in the canine arterial tree with particular reference to hemodynamic events. Circ Res. 1972; 30: 23–33.
Dewey CF, Gimbrone MA, Bussolari SR, Davies PF. The dynamic response of vascular endothelial cells to fluid shear stress. J Biomech Engin. 1981; 103: 177–185.
Remuzzi A, Dewey CF, Davies PF, Gimbrone MA. Orientation of endothelial cells in shear fields in vitro. Biorheology. 1984; 21: 617–630.
Butcher JT, Penrod AM, Garcia AJ, Nerem RM. Unique morphology and focal adhesion development of valvular endothelial cellsin static and fluid flow environments. Arterioscler Thromb Vasc Biol. 2004; 24: 1429–1434.
Deck JD. Endothelial cell orientation on aortic valve leaflets. Cardiovasc Res. 1986; 20: 760–767.
Chi JT, Chang HY, Haraldsen G, Jahnsen FL, Troyanskaya OG, Chang DS, Wang Z, Rockson SG, van de Rijn M, Botstein D, Brown PO. Endothelial cell diversity revealed by global expression profiling. Proc Natl Acad Sci U S A. 2003; 100: 10623–10628.
Topper JN, Gimbrone MA. Blood flow and vascular gene expression: fluid shear stress as a modulator of endothelial phenotype. Mol Med Today. 1999; 5: 40–46.
Garcia-Cardena G, Comander J, Anderson KR, Blackman BR, Gimbrone MA. Biomechanical activation of vascular endothelium as a determinant of its functional phenotype. Proc Natl Acad Sci U S A. 2001; 98: 4478–4485.
Hajra L, Evans AI, Chen M, Hyduk SJ, Collins T, Cybulsky MI. The NF-kappa B signal transduction pathway in aortic endothelial cells is primed for activation in regions predisposed to atherosclerotic lesion formation. Proc Natl Acad Sci U S A. 2000; 97: 9052–9057.
Passerini AG, Polacek DC, Shi C, Francesco NM, Manduchi E, Grant G, Pritchard WP, Powell SJ, Chang G, Stoeckert C, Davies PF. Coexisting pro-inflammatory and anti-oxidative endothelial transcription profiles in a disturbed flow region of the adult porcine aorta. Proc Natl Acad Sci U S A. 2004; 101: 2482–2487.
Jackman RW. Persistence of axial orientation cues in regenerating intima of cultured aortic explants. Nature. 1982; 296: 80–83.
Tzima E, del Pozo MA, Shattil SJ, Chien S, Schwartz MA. Activation of integrins in endothelial cells by fluid shear stress mediates Rho-dependent cytoskeletal alignment. Embo J. 2001; 20: 4639–4647.
Farivar RS, Cohn LH, Soltesz EG, Mihaljevic T, Rawn JD, Byrne JG. Transcriptional profiling and growth kinetics of endothelium reveals differences between cells derived from porcine aorta versus aortic valve. Eur J Cardiothorac Surg. 2003; 24: 527–534.
Polacek DC, Passerini AG, Shi C, Francesco NM, Manduchi E, Grant G, Powell SJ, Bischof H, Winkler H, Stoeckert C, Davies PF. Fidelity and enhanced sensitivity of differential transcription profiles following linear amplification of nanogram amounts of endothelial mRNA. Physiological Genomics. 2003; 13: 147–156.
Simmons CA, Zilberberg J, Francesco NM, Shi C, Riley R, Davies PF. Transcriptional profiles of endothelium from opposite sides of the aortic valve suggest a link between hemodynamics and valvular calcification. Cardiovasc Pathol. 2004; 13 (suppl.): 186.
Otto CM, Kuusisto J, Reichenbach DD, Gown AM, O’Brien KD. Characterization of the early lesion of ’degenerative’ valvular aortic stenosis. Histological and immunohistochemical studies. Circulation. 1994; 90: 844–853.
Gimbrone MA Jr, Anderson KR, Topper JN, Langille BL, Clowes AW, Bercel S, Davies MG, Stenmark KR, Frid MG, Weiser-Evans MC, Aldashev AA, Nemenoff RA, Majesky MW, Landerholm TE, Lu J, Ito WD, Arras M, Scholz D, Imhof B, Aurrand-Lions M, Schaper W, Nagel TE, Resnick N, Dewey CF, Davies PF. Special communication: the critical role of mechanical forces in blood vessel development, physiology and pathology. J Vasc Surg. 1999; 29: 1104–1151.
Davies PF, Polacek DC, Shi C, Helmke BP. The convergence of hemodynamics, genomics, and endothelial structure, in studies of the focal origin of atherosclerosis. Biorheology. 2002; 39: 299–306.
Sarphie TG. Surface responses of aortic valve endothelia from diet-induced, hypercholesterolemic rabbits. Atherosclerosis. 1985; 54: 283–299.
Tompkins RG, Schnitzer JJ, Yarmush ML. Macromolecular transport within heart valves. Circ Res. 1989; 64: 1213–1223.(Peter F. Davies; Anthony )
Aortic valve diseases are debilitating cardiovascular disorders associated with significant morbidity and mortality. Although there continue to be major efforts to improve the longevity of replacement valves and to improve tissue engineered substitutes,1 the underlying mechanisms that may be responsible for the initiation and development of valve pathology have received less attention than have other sclerosing cardiovascular diseases such as atherogenesis. The endothelium lining of the cardiovascular system plays an important regulatory role in vascular physiology and pathology. In similar fashion, the surfaces of valve leaflets are presumed to be generally protected (eg, anticoagulant) and regulated (eg, permeability) by the endothelium. The functional properties of endothelium or its presence/absence are associated with a variety of valve pathologies,2 and systemic endothelial dysfunction is linked to aortic valve calcification.3 However, only recently have cell and molecular studies focused on the characterization of valve endothelial phenotypes with the idea that some aspects of phenotypic change or dysfunction may contribute to valve pathologies, a situation analogous to atherogenesis.
See page 1429
During the cardiac cycle, the aortic valve endothelium is subjected to complex fluid dynamics that are distinctly different on each side of the valve. As has been described for many years, arterial endothelial alignment in vivo generally follows the measured or predicted shear stress direction,4 and endothelial cells in vitro align with the dominant direction of the applied shear stress.5 The responses, which are reversible,4,6 represent endothelial structural remodeling in response to hemodynamic shear stress. It might be expected that endothelial cells isolated from aortic valves and grown in tissue culture will behave in a similar manner as arterial endothelium. However, in this issue of Arteriosclerosis, Thrombosis, and Vascular Biology, Butcher et al7 demonstrate that aortic valve endothelium in culture exhibits a distinctly different response to directional flow than that shown by cultured arterial endothelium isolated from nearby regions of the aorta. The study was inspired by the observations made by Deck et al8 that endothelium on the ventricular aortic valve surface tends to align circumferentially with the free edge of the leaflets rather than in the direction of predicted maximum shear stress induced by systolic flow. The new studies show that over a 48 hour period, cultured aortic valve endothelial cells align perpendicular to, rather than parallel to, the flow direction. The alignment differences were associated with differences in signaling pathways. Although arterial endothelial cell alignment was dependent on both Rho-kinase and phosphatidylinositol 3-kinase (PI3K) pathways, valve endothelium appeared not to require activation of PI3K to align perpendicular to the flow. These findings are relevant to valve pathology and to the development of replacement tissues, as well as to the broader issues of endothelial phenotypic heterogeneity (Figure).
Endothelial heterogeneity scaled for valve vs artery, aortic side vs ventricular side of the aortic valve, and cell-to-cell variation within the monolayer of each side.
In normal mammals, endothelial phenotype appears to be determined by a combination of intrinsic programmed gene expression9 and local epigenetic or environmental factors. Of the latter, the influence of the local hemodynamic environment on phenotype in vitro10,11 and in vivo12,13 has clearly been demonstrated. Endothelial orientation is also subject to "contact guidance" by the underlying substrate in situ.14 Contact guidance is consistent with the physical continuity of extracellular matrix (ECM), focal adhesions, and cytoskeletal elements, connections that are important in the determination of cell morphology and cell differentiation. Cytoskeletal organization and focal adhesion biology are highly regulated by Rho-kinase and PI3K signaling pathways,15 which were noted to be different for valve versus arterial endothelium.7 Some memory of orientation may have been carried over to the cultured valve endothelial cells to direct the synthesis of oriented ECM in the experiments conducted by Butcher et al. However, if this were the case, the valve cells required the reintroduction of flow to activate such memory. Whatever the explanations for the valve cell alignment responses, the study demonstrates interesting phenotypic differences for cultured valve endothelium that have implications for endothelial biology in general as well as for cell source considerations and engineered phenotypes for tissue engineered valve substitutes. The useful applications of this finding, however, will best be realized by investigating differential endothelial phenotypes in greater detail and at improved spatial resolution within the valve structure itself (see below).
Global endothelial gene expression analysis is a powerful tool to investigate spatial heterogeneity of endothelial phenotypes in general. Farivar et al16 noted significant differences in transcriptionally active genes expressed by arterial and valve endothelial cells grown in primary culture. Although there was common expression of 55 activated genes (of 847 interrogated), an additional 48 active genes were expressed by only one or the other cell type. Phenotypic memory in culture was also recently noted by Chi et al9 in endothelial cells isolated from many different vascular locations and then cultured for up to 5 passages before transcriptional profiling. Remarkably, hierarchical clustering revealed patterns of gene expression that reflected some of the known properties of the cells in situ; arterial versus venous markers, microvascular characteristics, and even characteristics of vascular bed symmetry were identified. Intrinsic differential phenotypic properties of endothelium therefore appear to be established during development, then presumably reinforced, enhanced, and retained by cues present in the local environment. The extent to which the intrinsic differentiated phenotype is further regulated by local conditions, such as hemodynamic/biomechanical stimuli, can now be investigated globally at the level of gene expression and in a more limited way for candidate protein expression and activity.
Refinements of genomics techniques permit transcriptional profiling of small regions of endothelium reflective of the steady state in vivo.17 This has recently been used to address regional phenotypic differences as a function of hemodynamic characteristics in both arteries13 and heart valves.18 Passerini et al13 profiled endothelial cells isolated directly from arterial regions of disturbed and undisturbed flow in normal adult pigs to better define gene expression changes that underlie a predisposition to atherogenesis in regions of complex blood flow. The coexistence of pro- and antiinflammatory gene expression patterns in the same athero-susceptible locations was noted. This balance of opposing mechanisms suggests that endothelial cells were primed for an atherogenic inflammatory response but kept in check by compensatory mechanisms in the absence of additional risk factors. The studies identified arterial hemodynamics as a contributor to regional endothelial heterogeneity via multiple pathways and as a subtle risk factor for athero-susceptibility. A similar approach is currently being applied to differential phenotyping of heart valve endothelium.18 In this emerging work, the principal objective is to refine the spatial genomics to comparisons of each side of the valve leaflet because differential susceptibility to calcific sclerosis is side-specific.19 Calcification occurs preferentially in the aortic valve on the side that is exposed to more highly disturbed blood flow, suggestive of a role for hemodynamics in valvular calcification. Thus there are hemodynamic similarities to the disturbed flow characteristics that spatially correlate with regions of athero-susceptibility in large arteries.13,20 In paired comparisons of aortic side versus ventricular side endothelium, Simmons et al (manuscript in preparation) observed differential transcriptional profiles across multiple pathways, including prominent representation of proliferative, apoptotic, and calcification pathways. These early data suggest differential endothelial phenotypes that define the sidedness of the aortic valve, a significant improvement in spatial resolution for this tissue (Figure, middle). The approach also addresses the complex mechanisms associated with aortic-side susceptibility of the valve to sclerosis and calcification. Furthermore, it should be possible to contrast the in situ and intrinsic (cultured) phenotypes, because valve endothelium from each side can be cultured for comparison of gene expression profiles from the same tissues in vitro and in situ. A higher level of spatial resolution would be obtained by profiling single or small groupings of endothelial cells.21 There is ample evidence of cell-to-cell heterogeneity of endothelial morphology22 and transport properties23 throughout the aortic valve suggesting that phenotypic differences might be resolved at the single cell level (Figure, right).
In summary, the provocative observations noted by Butcher et al in culture reveal interesting differences in the responses to flow of the valve endothelium compared with the aortic endothelium. However, they likely represent merely the tip of the iceberg regarding valve endothelial phenotypes, and in situ endothelial heterogeneity in general.8,20 More detailed investigation of both valve and vascular bed endothelium is required by global phenotyping at the highest spatial resolution possible.
Vascular phenotyping research in the Davies laboratory is supported by National Institutes of Health (National Heart, Lung, and Blood Institute) grants HL36049 (MERIT), HL64388, and HL62250, National Aeronautics and Space Administration-National Space Biomedical Research Institute grant 01-102, National Institutes of Health Training grant HL07954 (to A.G.P.), and American Heart Association Postdoctoral Fellowship 0325666U (to C.A.S.).
References
Schoen FJ, Levy RJ. Tissue heart valves: current challenges and future research perspectives. J Biomed Mater Res. 1999; 47: 439–465.
Muller AM, Cronen C, Kupferwasser LI, Oelert H, Muller KM, Kirkpatrick CJ. Expression of endothelial cell adhesion molecules on heart valves: up-regulation in degeneration as well as acute endocarditis. J Pathol. 2000; 191: 54–60.
Poggianti E, Venneri L, Chubuchny V, Jambrik Z, Baroncini LA, Picano E. Aortic valve sclerosis is associated with systemic endothelial dysfunction. J Am Coll Cardiol. 2003; 41: 136–141.
Flaherty JT, Pierce JE, Ferrans VJ, Patel DJ, Tucker WK, Fry DL. Endothelial nuclear patterns in the canine arterial tree with particular reference to hemodynamic events. Circ Res. 1972; 30: 23–33.
Dewey CF, Gimbrone MA, Bussolari SR, Davies PF. The dynamic response of vascular endothelial cells to fluid shear stress. J Biomech Engin. 1981; 103: 177–185.
Remuzzi A, Dewey CF, Davies PF, Gimbrone MA. Orientation of endothelial cells in shear fields in vitro. Biorheology. 1984; 21: 617–630.
Butcher JT, Penrod AM, Garcia AJ, Nerem RM. Unique morphology and focal adhesion development of valvular endothelial cellsin static and fluid flow environments. Arterioscler Thromb Vasc Biol. 2004; 24: 1429–1434.
Deck JD. Endothelial cell orientation on aortic valve leaflets. Cardiovasc Res. 1986; 20: 760–767.
Chi JT, Chang HY, Haraldsen G, Jahnsen FL, Troyanskaya OG, Chang DS, Wang Z, Rockson SG, van de Rijn M, Botstein D, Brown PO. Endothelial cell diversity revealed by global expression profiling. Proc Natl Acad Sci U S A. 2003; 100: 10623–10628.
Topper JN, Gimbrone MA. Blood flow and vascular gene expression: fluid shear stress as a modulator of endothelial phenotype. Mol Med Today. 1999; 5: 40–46.
Garcia-Cardena G, Comander J, Anderson KR, Blackman BR, Gimbrone MA. Biomechanical activation of vascular endothelium as a determinant of its functional phenotype. Proc Natl Acad Sci U S A. 2001; 98: 4478–4485.
Hajra L, Evans AI, Chen M, Hyduk SJ, Collins T, Cybulsky MI. The NF-kappa B signal transduction pathway in aortic endothelial cells is primed for activation in regions predisposed to atherosclerotic lesion formation. Proc Natl Acad Sci U S A. 2000; 97: 9052–9057.
Passerini AG, Polacek DC, Shi C, Francesco NM, Manduchi E, Grant G, Pritchard WP, Powell SJ, Chang G, Stoeckert C, Davies PF. Coexisting pro-inflammatory and anti-oxidative endothelial transcription profiles in a disturbed flow region of the adult porcine aorta. Proc Natl Acad Sci U S A. 2004; 101: 2482–2487.
Jackman RW. Persistence of axial orientation cues in regenerating intima of cultured aortic explants. Nature. 1982; 296: 80–83.
Tzima E, del Pozo MA, Shattil SJ, Chien S, Schwartz MA. Activation of integrins in endothelial cells by fluid shear stress mediates Rho-dependent cytoskeletal alignment. Embo J. 2001; 20: 4639–4647.
Farivar RS, Cohn LH, Soltesz EG, Mihaljevic T, Rawn JD, Byrne JG. Transcriptional profiling and growth kinetics of endothelium reveals differences between cells derived from porcine aorta versus aortic valve. Eur J Cardiothorac Surg. 2003; 24: 527–534.
Polacek DC, Passerini AG, Shi C, Francesco NM, Manduchi E, Grant G, Powell SJ, Bischof H, Winkler H, Stoeckert C, Davies PF. Fidelity and enhanced sensitivity of differential transcription profiles following linear amplification of nanogram amounts of endothelial mRNA. Physiological Genomics. 2003; 13: 147–156.
Simmons CA, Zilberberg J, Francesco NM, Shi C, Riley R, Davies PF. Transcriptional profiles of endothelium from opposite sides of the aortic valve suggest a link between hemodynamics and valvular calcification. Cardiovasc Pathol. 2004; 13 (suppl.): 186.
Otto CM, Kuusisto J, Reichenbach DD, Gown AM, O’Brien KD. Characterization of the early lesion of ’degenerative’ valvular aortic stenosis. Histological and immunohistochemical studies. Circulation. 1994; 90: 844–853.
Gimbrone MA Jr, Anderson KR, Topper JN, Langille BL, Clowes AW, Bercel S, Davies MG, Stenmark KR, Frid MG, Weiser-Evans MC, Aldashev AA, Nemenoff RA, Majesky MW, Landerholm TE, Lu J, Ito WD, Arras M, Scholz D, Imhof B, Aurrand-Lions M, Schaper W, Nagel TE, Resnick N, Dewey CF, Davies PF. Special communication: the critical role of mechanical forces in blood vessel development, physiology and pathology. J Vasc Surg. 1999; 29: 1104–1151.
Davies PF, Polacek DC, Shi C, Helmke BP. The convergence of hemodynamics, genomics, and endothelial structure, in studies of the focal origin of atherosclerosis. Biorheology. 2002; 39: 299–306.
Sarphie TG. Surface responses of aortic valve endothelia from diet-induced, hypercholesterolemic rabbits. Atherosclerosis. 1985; 54: 283–299.
Tompkins RG, Schnitzer JJ, Yarmush ML. Macromolecular transport within heart valves. Circ Res. 1989; 64: 1213–1223.(Peter F. Davies; Anthony )