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Modeling Ca2+ Signaling in the Microcirculation: Intercellular Communication and Vasoreactivity

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Publisher Begell House
Date 2011 Dec 27
PMID 22196162
Citations 8
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Abstract

A network of intracellular signaling pathways and complex intercellular interactions regulate calcium mobilization in vascular cells, arteriolar tone, and blood flow. Different endothelium-derived vasoreactive factors have been identified and the importance of myoendothelial communication in vasoreactivity is now well appreciated. The ability of many vascular networks to conduct signals upstream also is established. This phenomenon is critical for both short-term changes in blood perfusion as well as long-term adaptations of a vascular network. In addition, in a phenomenon termed vasomotion, arterioles often exhibit spontaneous oscillations in diameter. This is thought to improve tissue oxygenation and enhance blood flow. Experimentation has begun to reveal important aspects of the regulatory machinery and the significance of these phenomena for the regulation of local perfusion and oxygenation. Mathematical modeling can assist in elucidating the complex signaling mechanisms that participate in these phenomena. This review highlights some of the important experimental studies and relevant mathematical models that provide the current understanding of these mechanisms in vasoreactivity.

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References
1.
Imtiaz M, von der Weid P, van Helden D . Synchronization of Ca2+ oscillations: a coupled oscillator-based mechanism in smooth muscle. FEBS J. 2009; 277(2):278-85. DOI: 10.1111/j.1742-4658.2009.07437.x. View

2.
De Young G, Keizer J . A single-pool inositol 1,4,5-trisphosphate-receptor-based model for agonist-stimulated oscillations in Ca2+ concentration. Proc Natl Acad Sci U S A. 1992; 89(20):9895-9. PMC: 50240. DOI: 10.1073/pnas.89.20.9895. View

3.
Schmidt J, Intaglietta M, Borgstrom P . Periodic hemodynamics in skeletal muscle during local arterial pressure reduction. J Appl Physiol (1985). 1992; 73(3):1077-83. DOI: 10.1152/jappl.1992.73.3.1077. View

4.
Schuster A, Oishi H, Beny J, Stergiopulos N, Meister J . Simultaneous arterial calcium dynamics and diameter measurements: application to myoendothelial communication. Am J Physiol Heart Circ Physiol. 2001; 280(3):H1088-96. DOI: 10.1152/ajpheart.2001.280.3.H1088. View

5.
Sandow S, Tare M, Coleman H, Hill C, Parkington H . Involvement of myoendothelial gap junctions in the actions of endothelium-derived hyperpolarizing factor. Circ Res. 2002; 90(10):1108-13. DOI: 10.1161/01.res.0000019756.88731.83. View