Abstract
The extracellular presence of the adenine nucleotides ATP and ADP induces calcium mobilization in vascular endothelial cells (ECs). ATP/ADP concentration at the EC surface is determined by a balance of convective-diffusive transport to and from the EC surface, hydrolysis by ectonucleotidases at the cell surface, and flow-induced ATP release from ECs. Our previous numerical simulations in a parallel plate geometry had demonstrated that flow-induced ATP release has a profound effect on nucleotide concentration at the EC surface. In the present study, we have extended the modeling to probe the impact of flow separation and recirculation downstream of a backward facing step (BFS) on ATP/ADP concentration at the EC surface. The results show that for both steady and pulsatile flow over a wide range of wall shear stresses, the ATP + ADP concentration at the EC surface is considerably lower within the flow recirculation region than in areas of undisturbed flow outside the recirculation zone. Pulsatile flow also leads to sharp temporal gradients in nucleotide concentration. If confirmed experimentally, the present findings suggest that disturbed and undisturbed flow may affect EC calcium mobilization differently. Such differences might, in turn, contribute to the observed endothelial dysfunction in regions of disturbed flow.
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References
Ando J., A. Ohtsuka, R. Korenaga, A. Kamiya. Effect of extracellular ATP level on flow-induced Ca++ response in cultured vascular endothelial cells Biochem. Biophys. Res. Commun. 179:1192–1199, 1991
Armaly B. F., F. Durst, J. C. F. Pereira, B. Schonung. Experimental and theoretical investigation of backward-facing step flow J. Fluid Mech. 127:473–496, 1983
Barakat A. I., T. Karino, C. K. Colton. Microcinematographic studies of flow patterns in the excised rabbit aorta and its major branches Biorheology 34:195–221, 1997
Barakat A. I., D. K. Lieu. Differential responsiveness of vascular endothelial cells to different types of fluid mechanical shear stress Cell Biochem. Biophys. 38:323–343, 2003
Bodin P., G. Burnstock. ATP-stimulated release of ATP by human endothelial cells J. Cardiovasc Pharmacol. 27:872–875, 1996
Bodin P., G. Burnstock. Evidence that release of adenosine triphosphate from endothelial cells during increased shear stress is vesicular J. Cardiovasc. Pharmacol. 38:900–908, 2001
Burnstock G., C. Kennedy. A dual function for adenosine 5′-triphosphate in the regulation of vascular tone. Excitatory cotransmitter with noradrenaline from perivascular nerves and locally released inhibitory intravascular agent Circ. Res. 58: 319–330,1986
Choi H. W., A. I. Barakat. Numerical study of the impact of non-newtonian blood behavior on flow over a two-dimensional backward facing step Biorheology 42:493–509, 2005
Cusack N. J., J. D. Pearson, J. L. Gordon. Stereoselectivity of ectonucleotidases on vascular endothelial cells Biochem. J. 214:975–981, 1983
David T. Wall shear stress modulation of ATP/ADP concentration at the endothelium Ann. Biomed. Eng. 31:1231–1237, 2003
Davies P. F. Flow-mediated endothelial mechanotransduction Physiol Rev. 75:519–560, 1995
DePaola N., P. F. Davies, W. F. Pritchard Jr., L. Florez, N. Harbeck, D. C. Polacek. Spatial and temporal regulation of gap junction connexin43 in vascular endothelial cells exposed to controlled disturbed flows in vitro Proc. Natl. Acad. Sci. U S A 96:3154–3159, 1999
DePaola N., M. A. Gimbrone Jr., P. F. Davies, C. F. Dewey Jr. Vascular endothelium responds to fluid shear stress gradients Arterioscler Thromb. 12:1254–1257, 1992
Dull R. O., P. F. Davies. Flow modulation of agonist (ATP)-response (Ca2+) coupling in vascular endothelial cells Am. J. Physiol. 261:H149–154, 1991
Geiger R. V., B. C. Berk, R. W. Alexander, R. M. Nerem. Flow-induced calcium transients in single endothelial cells: Spatial and temporal analysis Am. J. Physiol. 262:C1411–C1417, 1992
Haidekker M. A., C. R. White, J. A. Frangos. Analysis of temporal shear stress gradients during the onset phase of flow over a backward-facing step J. Biomech. Eng. 123:455–463, 2001
Helmlinger G., B. C. Berk, R. M. Nerem. Calcium responses of endothelial cell monolayers subjected to pulsatile and steady laminar flow differ Am. J. Physiol. 269:C367–C375, 1995
Hsu P. P., S. Li, Y. S. Li, S. Usami, A. Ratcliffe, X. Wang, S. Chien. Effects of flow patterns on endothelial cell migration into a zone of mechanical denudation Biochem. Biophys. Res. Commun 285: 751–759, 2001
John K., A. I. Barakat. Modulation of ATP/ADP concentration at the endothelial surface by shear stress: Effect of flow-induced ATP release Ann. Biomed. Eng. 29:740–751, 2001
Ku D. N., D. P. Giddens, C. K. Zarins, S. Glagov. Pulsatile flow and atherosclerosis in the human carotid bifurcation: Positive correlation between plaque location and low oscillating shear stress Arteriosclerosis 5:293–302, 1985
Lei M., C. Kleinstreuer, G. A. Truskey. Numerical investigation and prediction of atherogenic sites in branching arteries J. Biomech. Eng. 117:350–357, 1995
Milner P., K. A. Kirkpatrick, V. Ralevic, V. Toothill, J. Pearson, G. Burnstock. Endothelial cells cultured from human umbilical vein release ATP, substance P and acetylcholine in response to increased flow Proc. Biol. Sci. 241:245–248, 1990
Mo M., S. G. Eskin, W. P. Schilling. Flow-induced changes in Ca2+ signaling of vascular endothelial cells: Effect of shear stress and ATP Am. J. Physiol. 260:H1698–H1707, 1991
Moore J. E. Jr., C. Xu, S. Glagov, C. K. Zarins, D. N. Ku. Fluid wall shear stress measurements in a model of the human abdominal aorta: Oscillatory behavior and relationship to atherosclerosis Atherosclerosis 110:225–240, 1994
Nerem R. M. Vascular fluid mechanics, the arterial wall, and atherosclerosis J. Biomech. Eng. 114:274–282, 1992
Nollert M. U., S. L. Diamond, L. V. Mcintire. Hydrodynamic shear-stress and mass-transport modulation of endothelial-cell metabolism Biotechnol. Bioeng. 38:588–602, 1991
Nollert M. U., L. V. McIntire. Convective mass transfer effects on the intracellular calcium response of endothelial cells J. Biomech. Eng. 114:321–326, 1992
Olsson R. A., J. D. Pearson. Cardiovascular purinoceptors Physiol. Rev. 70:761–845, 1990
Pearson J. D., J. L. Gordon. Vascular endothelial and smooth muscle cells in culture selectively release adenine nucleotides Nature 281:384–386, 1979
Pirotton S., E. Raspe, D. Demolle, C. Erneux, J. M. Boeynaems. Involvement of inositol 1,4,5-trisphosphate and calcium in the action of adenine nucleotides on aortic endothelial cells J. Biol. Chem. 262:17461–17466, 1987
Plank M. J., A. Comerford, T. David, D. J. N. Wall. Concentration of blood-borne agonists at the endothelium Proc. Royal. Soc. A 462:671–688, 2006
Plank M. J., D. J. N. Wall, T. David. Atherosclerosis and calcium signaling in endothelial cells Prog. Biophy. Mol. Bio. 91:287–313, 2006
Pohl U., J. Holtz, R. Busse, E. Bassenge. Crucial role of endothelium in the vasodilator response to increased flow in vivo Hypertension 8:37–44, 1986
Shen J., M. A. Gimbrone Jr., F. W. Luscinskas, C. F. Dewey Jr. Regulation of adenine nucleotide concentration at endothelium-fluid interface by viscous shear flow Biophys. J. 64:1323–1330, 1993
Shen J., F. W. Luscinskas, A. Connolly, C. F. Dewey Jr., M. A. Gimbrone Jr. Fluid shear stress modulates cytosolic free calcium in vascular endothelial cells Am. J. Physiol. 262:C384–C390, 1992
Truskey G. A., K. M. Barber, T. C. Robey, L. A. Olivier, M. P. Combs. Characterization of a sudden expansion flow chamber to study the response of endothelium to flow recirculation J. Biomech. Eng. 117:203–210, 1995
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This work is supported in part by grants from the National Institutes of Health (NIH CA 103828) and Philip Morris, USA.
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Choi, H.W., Ferrara, K.W. & Barakat, A.I. Modulation of ATP/ADP Concentration at the Endothelial Surface by Shear Stress: Effect of Flow Recirculation. Ann Biomed Eng 35, 505–516 (2007). https://doi.org/10.1007/s10439-006-9247-9
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DOI: https://doi.org/10.1007/s10439-006-9247-9