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Kinetics of Extracellular ATP from Goldfish Hepatocytes: A Lesson from Mathematical Modeling

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Abstract

In goldfish hepatocytes, hypotonic exposure leads to cell swelling, followed by a compensatory shrinkage termed RVD. It has been previously shown that ATP is accumulated in the extracellular medium of swollen cells in a non-linear fashion, and that extracellular ATP (ATPe) is an essential intermediate to trigger RVD.

Thus, to understand how RVD proceeds in goldfish hepatocytes, we developed two mathematical models accounting for the experimental ATPe kinetics reported recently by Pafundo et al. in Am. J. Physiol. 294, R220–R233, 2008. Four different equations for ATPe fluxes were built to account for the release of ATP by lytic (J L ) and nonlytic mechanisms (J NL ), ATPe diffusion (J D ), and ATPe consumption by ectonucleotidases (J V ). Particular focus was given to J NL , defined as the product of a time function (J R ) and a positive feedback mechanism whereby ATPe amplifies J NL . Several J R functions (Constant, Step, Impulse, Gaussian, and Lognormal) were studied. Models were tested without (model 1) or with (model 2) diffusion of ATPe.

Mathematical analysis allowed us to get a general expression for each of the models. Subsequently, by using model dependent fit (simulations) as well as model analysis at infinite time, we observed that:

  1. use of J D does not lead to improvements of the models.

  2. Constant and Step time functions are only applicable when J R =0 (and thus, J NL =0), so that the only source of ATPe would be J L , a result incompatible with experimental data.

  3. use of impulse, Gaussian, and lognormal J R s in the models led to reasonable good fits to experimental data, with the lognormal function in model 1 providing the best option.

Finally, the predictive nature of model 1 loaded with a lognormal J R was tested by simulating different putative in vivo scenarios where J V and J NL were varied over ample ranges.

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References

  • Akaike, H., 1992. Data analysis by statistical models. No To Hattatsu 24, 127–133.

    Google Scholar 

  • Alleva, K.E., Espelt, M.E., Krumschnabel, G., Schwarzbaum, P.J., 2002. Identification of two distinct E-NTPDases in liver of goldfish (Carassius auratus L.). Comp. Biochem. Physiol. 131, 725–731.

    Google Scholar 

  • Anderson, C.M., Bergher, J.P., Swanson, R.A., 2004. ATP-induced ATP release from astrocytes. J. Neurochem. 88, 246–256.

    Article  Google Scholar 

  • Burnstock, G., 2006. Purinergic signalling. Br. J. Pharmacol. 147, 172–181.

    Article  Google Scholar 

  • Burnstock, G., 2007. Physiology and pathophysiology of purinergic neurotransmission. Physiol. Rev. 87, 659–797.

    Article  Google Scholar 

  • Chessell, I.P., Hatcher, J.P., Bountra, C., Michel, A.D., Hughes, J.P., Green, P., Egerton, J., Murfin, M., Richardson, J., Peck, W.L., Grahames, C.B., Casula, M.A., Yiangou, Y., Birch, R., Anand, P., Buell, G.N., 2005. Disruption of the P2X7 purinoceptor gene abolishes chronic inflammatory and neuropathic pain. Pain 114, 386–396.

    Article  Google Scholar 

  • Dainty, J., 1963. The polar permeability of plant cell membranes to water. Protoplasma 1, 220–228.

    Article  Google Scholar 

  • Dainty, J., House, C.R., 1966. Unstirred layers in frog skin. J. Physiol. 182, 66–78.

    Google Scholar 

  • Finkelstein, A., 1987. Water Movement through Lipid Bilayers, Pores, and Plasma Membranes. Wiley, New York.

    Google Scholar 

  • Haussinger, D., 1996. The role of cellular hydration in the regulation of cell function. Biochem. J. 313, 697–710.

    Google Scholar 

  • Hernández, J.A., Cristina, E., 1998. Modeling cell volume regulation in nonexcitable cells: the roles of the Na+ pump and of cotransport systems. Am. J. Physiol. 275, 1067–1080.

    Google Scholar 

  • Hubley, M.J., Locke, B.R., Moerland, T.S., 1996. The effects of temperature, pH, and magnesium on the diffusion coefficient of ATP in solutions of physiological ionic strength. Biochim. Biophys. Acta 1291, 115–121.

    Google Scholar 

  • Jakab, M., Fürst, J., Gschwentner, M., Bottà, G., Garavaglia, M.L., Bazzini, C., Rodighiero, S., Meyer, G., Eichmüller, S., Wöll, E., Chwatal, S., Ritter, M., Paulmichl, M., 2002. Mechanisms sensing and modulating signals arising from cell swelling. Cell. Physiol. Biochem. 12, 235–258.

    Article  Google Scholar 

  • Jans, D., Srinivas, S.P., Waelkens, E., Segal, A., Larivière, E., Simaels, J., Van Driessche, W., 2002. Hypotonic treatment evokes biphasic ATP release across the basolateral membrane of cultured renal epithelia (A6). J. Physiol. 545, 543–555.

    Article  Google Scholar 

  • Lazarowski, E.R., Boucher, R.C., Harden, T.K., 2003. Mechanisms of release of nucleotides and integration of their action as P2X- and P2Y-receptor activating molecules. Mol. Pharmacol. 64, 785–795.

    Article  Google Scholar 

  • Okada, Y., Maeno, E., Shimizu, T., Dezaki, K., Wang, J., Morishima, S., 2001. Receptor-mediated control of regulatory volume decrease (RVD) and apoptotic volume decrease (AVD). J. Physiol. 532, 3–16.

    Article  Google Scholar 

  • Pafundo, D.E., Mut, P., Pérez Recalde, M., González-Lebrero, R.M., Fachino, V., Krumschnabel, G., Schwarzbaum, P.J., 2004. Effects of extracellular nucleotides and their hydrolysis products on regulatory volume decrease of trout hepatocytes. Am. J. Physiol. 287, 833–843.

    Google Scholar 

  • Pafundo, D.E., Chara, O., Faillace, M.P., Krumschnabel, G., Schwarzbaum, P.J., 2008. Kinetics of ATP release and cell volume regulation of hyposmotically challenged goldfish hepatocytes. Am. J. Physiol. 294, 220–233.

    Google Scholar 

  • Pohl, P., Saparov, S.M., Antonenko, Y.N., 1998. The effect of a transmembrane osmotic flux on the ion concentration distribution in the immediate membrane vicinity measured by microelectrodes. Biophys. J. 72, 1711–1718.

    Article  Google Scholar 

  • Sabirov, R.Z., Okada, Y., 2005. ATP release via anion channels. Purinergic Signal. 1, 311–328.

    Article  Google Scholar 

  • Schulman, J.H., Teorell, T., 1938. On the boundary layer at membrane and monolayer interfaces. Trans. Faraday Soc. 34, 1337–1342.

    Article  Google Scholar 

  • Schwarzbaum, P.J., Frischmann, M.E., Krumschnabel, G., Rossi, R.C., Wieser, W., 1998. Functional role of ecto-ATPase activity in goldfish hepatocytes. Am. J. Physiol. 274, 1031–1038.

    Google Scholar 

  • Suadicani, S.O., Brosnan, C.F., Scemes, E., 2006. P2X7 receptors mediate ATP release and amplification of astrocytic intercellular Ca2+ signaling. J. Neurosci. 26, 1378–1385.

    Article  Google Scholar 

  • Wang, Y., Roman, R., Lidofsky, S.D., Fitz, J.G., 1996. Autocrine signaling through ATP release represents a novel mechanism for cell volume regulation. Proc. Natl. Acad. Sci. 93, 12020–12025.

    Article  Google Scholar 

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Correspondence to Pablo J. Schwarzbaum.

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Chara, O., Pafundo, D.E. & Schwarzbaum, P.J. Kinetics of Extracellular ATP from Goldfish Hepatocytes: A Lesson from Mathematical Modeling. Bull. Math. Biol. 71, 1025–1047 (2009). https://doi.org/10.1007/s11538-008-9392-4

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