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      Heterogeneous ATP patterns in microvascular networks

      1 , 1 , 2 , 1
      Journal of The Royal Society Interface
      The Royal Society

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          Abstract

          ATP is not only an energy carrier but also serves as an important signalling molecule in many physiological processes. Abnormal ATP level in blood vessel is known to be related to several pathologies, such as inflammation, hypoxia and atherosclerosis. Using advanced numerical methods, we analysed ATP released by red blood cells (RBCs) and its degradation by endothelial cells (ECs) in a cat mesentery-inspired vascular network, accounting for RBC mutual interaction and interactions with vascular walls. Our analysis revealed a heterogeneous ATP distribution in the network, with higher concentrations in the cell-free layer, concentration peaks around bifurcations and heterogeneity among vessels of the same level. These patterns arise from the spatio-temporal organization of RBCs induced by the network geometry. It is further shown that an alteration of hematocrit and flow strength significantly affects ATP level as well as heterogeneity in the network. These findings constitute a first building block to elucidate the intricate nature of ATP patterns in vascular networks and the far reaching consequences for other biochemical signalling, such as calcium, by ECs.

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          Most cited references75

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          2021 ESC Guidelines for the diagnosis and treatment of acute and chronic heart failure

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            Hemodynamic shear stress and its role in atherosclerosis.

            Adel Malek (1999)
            Atherosclerosis, the leading cause of death in the developed world and nearly the leading cause in the developing world, is associated with systemic risk factors including hypertension, smoking, hyperlipidemia, and diabetes mellitus, among others. Nonetheless, atherosclerosis remains a geometrically focal disease, preferentially affecting the outer edges of vessel bifurcations. In these predisposed areas, hemodynamic shear stress, the frictional force acting on the endothelial cell surface as a result of blood flow, is weaker than in protected regions. Studies have identified hemodynamic shear stress as an important determinant of endothelial function and phenotype. Arterial-level shear stress (>15 dyne/cm2) induces endothelial quiescence and an atheroprotective gene expression profile, while low shear stress (<4 dyne/cm2), which is prevalent at atherosclerosis-prone sites, stimulates an atherogenic phenotype. The functional regulation of the endothelium by local hemodynamic shear stress provides a model for understanding the focal propensity of atherosclerosis in the setting of systemic factors and may help guide future therapeutic strategies.
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              Phenotypic heterogeneity of the endothelium: I. Structure, function, and mechanisms.

              Endothelial cells, which form the inner cellular lining of blood vessels and lymphatics, display remarkable heterogeneity in structure and function. This is the first of a 2-part review focused on phenotypic heterogeneity of blood vessel endothelium. This review provides an historical perspective of our understanding of endothelial heterogeneity, discusses the scope of phenotypic diversity across the vascular tree, and addresses proximate and evolutionary mechanisms of endothelial cell heterogeneity. The overall goal is to underscore the importance of phenotypic heterogeneity as a core property of the endothelium.
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                Author and article information

                Contributors
                Journal
                Journal of The Royal Society Interface
                J. R. Soc. Interface.
                The Royal Society
                1742-5662
                July 2023
                July 19 2023
                July 2023
                : 20
                : 204
                Affiliations
                [1 ]CNRS, LIPhy, Université Grenoble Alpes, 38000 Grenoble, France
                [2 ]Shenzhen Sibionics Co. Ltd, Shenzhen, People’s Republic of China
                Article
                10.1098/rsif.2023.0186
                10354495
                37464803
                702c36a1-48ff-40a0-9890-09d86e31b9c9
                © 2023

                https://royalsociety.org/journals/ethics-policies/data-sharing-mining/

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