Abstract
Stimulation of hepatocytes with vasopressin evokes increases in cytosolic free Ca2+ ([Ca2+]c) that are relayed into the mitochondria, where the resulting mitochondrial Ca2+ ([Ca2+]m) increase regulates intramitochondrial Ca2+-sensitive targets. To understand how mitochondria integrate the [Ca2+]c signals into a final metabolic response, we stimulated hepatocytes with high vasopressin doses that generate a sustained increase in [Ca2+]c. This elicited a synchronous, single spike of [Ca2+]m and consequent NAD(P)H formation, which could be related to changes in the activity state of pyruvate dehydrogenase (PDH) measured in parallel. The vasopressin-induced [Ca2+]m spike evoked a transient increase in NAD(P)H that persisted longer than the [Ca2+]m increase. In contrast, PDH activity increased biphasically, with an initial rapid phase accompanying the rise in [Ca2+]m, followed by a sustained secondary activation phase associated with a decline in cellular ATP. The decline of NAD(P)H in the face of elevated PDH activity occurred as a result of respiratory chain activation, which was also manifest in a calcium-dependent increase in the membrane potential and pH gradient components of the proton motive force (PMF). This is the first direct demonstration that Ca2+-mobilizing hormones increase the PMF in intact cells. Thus, Ca2+ plays an important role in signal transduction from cytosol to mitochondria, with a single [Ca2+]m spike evoking a complex series of changes to activate mitochondrial oxidative metabolism.
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- Babcock D. F., Herrington J., Goodwin P. C., Park Y. B., Hille B. Mitochondrial participation in the intracellular Ca2+ network. J Cell Biol. 1997 Feb 24;136(4):833–844. doi: 10.1083/jcb.136.4.833. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balaban R. S., Blum J. J. Hormone-induced changes in NADH fluorescence and O2 consumption of rat hepatocytes. Am J Physiol. 1982 Mar;242(3):C172–C177. doi: 10.1152/ajpcell.1982.242.3.C172. [DOI] [PubMed] [Google Scholar]
- Bradford M. M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976 May 7;72:248–254. doi: 10.1006/abio.1976.9999. [DOI] [PubMed] [Google Scholar]
- Brini M., Marsault R., Bastianutto C., Alvarez J., Pozzan T., Rizzuto R. Transfected aequorin in the measurement of cytosolic Ca2+ concentration ([Ca2+]c). A critical evaluation. J Biol Chem. 1995 Apr 28;270(17):9896–9903. doi: 10.1074/jbc.270.17.9896. [DOI] [PubMed] [Google Scholar]
- Brini M., Marsault R., Bastianutto C., Pozzan T., Rizzuto R. Nuclear targeting of aequorin. A new approach for measuring nuclear Ca2+ concentration in intact cells. Cell Calcium. 1994 Oct;16(4):259–268. doi: 10.1016/0143-4160(94)90089-2. [DOI] [PubMed] [Google Scholar]
- Brown G. C., Lakin-Thomas P. L., Brand M. D. Control of respiration and oxidative phosphorylation in isolated rat liver cells. Eur J Biochem. 1990 Sep 11;192(2):355–362. doi: 10.1111/j.1432-1033.1990.tb19234.x. [DOI] [PubMed] [Google Scholar]
- Budd S. L., Nicholls D. G. A reevaluation of the role of mitochondria in neuronal Ca2+ homeostasis. J Neurochem. 1996 Jan;66(1):403–411. doi: 10.1046/j.1471-4159.1996.66010403.x. [DOI] [PubMed] [Google Scholar]
- Chiavaroli C., Bird G., Putney J. W., Jr Delayed "all-or-none" activation of inositol 1,4,5-trisphosphate-dependent calcium signaling in single rat hepatocytes. J Biol Chem. 1994 Oct 14;269(41):25570–25575. [PubMed] [Google Scholar]
- Davidson A. M., Halestrap A. P. Liver mitochondrial pyrophosphate concentration is increased by Ca2+ and regulates the intramitochondrial volume and adenine nucleotide content. Biochem J. 1987 Sep 15;246(3):715–723. doi: 10.1042/bj2460715. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Denton R. M., McCormack J. G. On the role of the calcium transport cycle in heart and other mammalian mitochondria. FEBS Lett. 1980 Sep 22;119(1):1–8. doi: 10.1016/0014-5793(80)80986-0. [DOI] [PubMed] [Google Scholar]
- Denton R. M., McCormack J. G., Rutter G. A., Burnett P., Edgell N. J., Moule S. K., Diggle T. A. The hormonal regulation of pyruvate dehydrogenase complex. Adv Enzyme Regul. 1996;36:183–198. doi: 10.1016/0065-2571(95)00020-8. [DOI] [PubMed] [Google Scholar]
- Denton R. M., Randle P. J., Martin B. R. Stimulation by calcium ions of pyruvate dehydrogenase phosphate phosphatase. Biochem J. 1972 Jun;128(1):161–163. doi: 10.1042/bj1280161. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Denton R. M., Richards D. A., Chin J. G. Calcium ions and the regulation of NAD+-linked isocitrate dehydrogenase from the mitochondria of rat heart and other tissues. Biochem J. 1978 Dec 15;176(3):899–906. doi: 10.1042/bj1760899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Duchen M. R. Ca(2+)-dependent changes in the mitochondrial energetics in single dissociated mouse sensory neurons. Biochem J. 1992 Apr 1;283(Pt 1):41–50. doi: 10.1042/bj2830041. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gunter T. E., Gunter K. K., Sheu S. S., Gavin C. E. Mitochondrial calcium transport: physiological and pathological relevance. Am J Physiol. 1994 Aug;267(2 Pt 1):C313–C339. doi: 10.1152/ajpcell.1994.267.2.C313. [DOI] [PubMed] [Google Scholar]
- Hajnóczky G., Robb-Gaspers L. D., Seitz M. B., Thomas A. P. Decoding of cytosolic calcium oscillations in the mitochondria. Cell. 1995 Aug 11;82(3):415–424. doi: 10.1016/0092-8674(95)90430-1. [DOI] [PubMed] [Google Scholar]
- Halestrap A. P., Dunlop J. L. Intramitochondrial regulation of fatty acid beta-oxidation occurs between flavoprotein and ubiquinone. A role for changes in the matrix volume. Biochem J. 1986 Nov 1;239(3):559–565. doi: 10.1042/bj2390559. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Halestrap A. P. The regulation of the matrix volume of mammalian mitochondria in vivo and in vitro and its role in the control of mitochondrial metabolism. Biochim Biophys Acta. 1989 Mar 23;973(3):355–382. doi: 10.1016/s0005-2728(89)80378-0. [DOI] [PubMed] [Google Scholar]
- Hansford R. G. Physiological role of mitochondrial Ca2+ transport. J Bioenerg Biomembr. 1994 Oct;26(5):495–508. doi: 10.1007/BF00762734. [DOI] [PubMed] [Google Scholar]
- Hems D. A., McCormack J. G., Denton R. M. Activation of pyruvate dehydrogenase in the perfused rat liver by vasopressin. Biochem J. 1978 Nov 15;176(2):627–629. doi: 10.1042/bj1760627. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hoek J. B., Nicholls D. G., Williamson J. R. Determination of the mitochondrial protonmotive force in isolated hepatocytes. J Biol Chem. 1980 Feb 25;255(4):1458–1464. [PubMed] [Google Scholar]
- Hoth M., Fanger C. M., Lewis R. S. Mitochondrial regulation of store-operated calcium signaling in T lymphocytes. J Cell Biol. 1997 May 5;137(3):633–648. doi: 10.1083/jcb.137.3.633. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jouaville L. S., Ichas F., Holmuhamedov E. L., Camacho P., Lechleiter J. D. Synchronization of calcium waves by mitochondrial substrates in Xenopus laevis oocytes. Nature. 1995 Oct 5;377(6548):438–441. doi: 10.1038/377438a0. [DOI] [PubMed] [Google Scholar]
- Loew L. M., Carrington W., Tuft R. A., Fay F. S. Physiological cytosolic Ca2+ transients evoke concurrent mitochondrial depolarizations. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12579–12583. doi: 10.1073/pnas.91.26.12579. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Loew L. M., Tuft R. A., Carrington W., Fay F. S. Imaging in five dimensions: time-dependent membrane potentials in individual mitochondria. Biophys J. 1993 Dec;65(6):2396–2407. doi: 10.1016/S0006-3495(93)81318-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McCormack J. G., Denton R. M. The effects of calcium ions and adenine nucleotides on the activity of pig heart 2-oxoglutarate dehydrogenase complex. Biochem J. 1979 Jun 15;180(3):533–544. doi: 10.1042/bj1800533. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McCormack J. G., Halestrap A. P., Denton R. M. Role of calcium ions in regulation of mammalian intramitochondrial metabolism. Physiol Rev. 1990 Apr;70(2):391–425. doi: 10.1152/physrev.1990.70.2.391. [DOI] [PubMed] [Google Scholar]
- McCormack J. G. Studies on the activation of rat liver pyruvate dehydrogenase and 2-oxoglutarate dehydrogenase by adrenaline and glucagon. Role of increases in intramitochondrial Ca2+ concentration. Biochem J. 1985 Nov 1;231(3):597–608. doi: 10.1042/bj2310597. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Nicholls D. G. The regulation of extramitochondrial free calcium ion concentration by rat liver mitochondria. Biochem J. 1978 Nov 15;176(2):463–474. doi: 10.1042/bj1760463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oviasu O. A., Whitton P. D. Hormonal control of pyruvate dehydrogenase activity in rat liver. Biochem J. 1984 Nov 15;224(1):181–186. doi: 10.1042/bj2240181. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Owen M. R., Halestrap A. P. The mechanisms by which mild respiratory chain inhibitors inhibit hepatic gluconeogenesis. Biochim Biophys Acta. 1993 Apr 5;1142(1-2):11–22. doi: 10.1016/0005-2728(93)90079-u. [DOI] [PubMed] [Google Scholar]
- Pralong W. F., Spät A., Wollheim C. B. Dynamic pacing of cell metabolism by intracellular Ca2+ transients. J Biol Chem. 1994 Nov 4;269(44):27310–27314. [PubMed] [Google Scholar]
- Prpić V., Spencer T. L., Bygrave F. L. Stable enhancement of calcium retention in mitochondria isolated from rat liver after the administration of glucagon to the intact animal. Biochem J. 1978 Dec 15;176(3):705–714. doi: 10.1042/bj1760705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Quinlan P. T., Halestrap A. P. The mechanism of the hormonal activation of respiration in isolated hepatocytes and its importance in the regulation of gluconeogenesis. Biochem J. 1986 Jun 15;236(3):789–800. doi: 10.1042/bj2360789. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rizzuto R., Bastianutto C., Brini M., Murgia M., Pozzan T. Mitochondrial Ca2+ homeostasis in intact cells. J Cell Biol. 1994 Sep;126(5):1183–1194. doi: 10.1083/jcb.126.5.1183. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rizzuto R., Brini M., Murgia M., Pozzan T. Microdomains with high Ca2+ close to IP3-sensitive channels that are sensed by neighboring mitochondria. Science. 1993 Oct 29;262(5134):744–747. doi: 10.1126/science.8235595. [DOI] [PubMed] [Google Scholar]
- Robb-Gaspers L. D., Thomas A. P. Coordination of Ca2+ signaling by intercellular propagation of Ca2+ waves in the intact liver. J Biol Chem. 1995 Apr 7;270(14):8102–8107. doi: 10.1074/jbc.270.14.8102. [DOI] [PubMed] [Google Scholar]
- Rooney T. A., Sass E. J., Thomas A. P. Characterization of cytosolic calcium oscillations induced by phenylephrine and vasopressin in single fura-2-loaded hepatocytes. J Biol Chem. 1989 Oct 15;264(29):17131–17141. [PubMed] [Google Scholar]
- Rutter G. A., Burnett P., Rizzuto R., Brini M., Murgia M., Pozzan T., Tavaré J. M., Denton R. M. Subcellular imaging of intramitochondrial Ca2+ with recombinant targeted aequorin: significance for the regulation of pyruvate dehydrogenase activity. Proc Natl Acad Sci U S A. 1996 May 28;93(11):5489–5494. doi: 10.1073/pnas.93.11.5489. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rutter G. A. Ca2(+)-binding to citrate cycle dehydrogenases. Int J Biochem. 1990;22(10):1081–1088. doi: 10.1016/0020-711x(90)90105-c. [DOI] [PubMed] [Google Scholar]
- Rutter G. A., Theler J. M., Murgia M., Wollheim C. B., Pozzan T., Rizzuto R. Stimulated Ca2+ influx raises mitochondrial free Ca2+ to supramicromolar levels in a pancreatic beta-cell line. Possible role in glucose and agonist-induced insulin secretion. J Biol Chem. 1993 Oct 25;268(30):22385–22390. [PubMed] [Google Scholar]
- Simpson P. B., Russell J. T. Mitochondria support inositol 1,4,5-trisphosphate-mediated Ca2+ waves in cultured oligodendrocytes. J Biol Chem. 1996 Dec 27;271(52):33493–33501. doi: 10.1074/jbc.271.52.33493. [DOI] [PubMed] [Google Scholar]
- Soboll S., Horst C., Hummerich H., Schumacher J. P., Seitz H. J. Mitochondrial metabolism in different thyroid states. Biochem J. 1992 Jan 1;281(Pt 1):171–173. doi: 10.1042/bj2810171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soboll S. Long-term and short-term changes in mitochondrial parameters by thyroid hormones. Biochem Soc Trans. 1993 Aug;21(3):799–803. doi: 10.1042/bst0210799. [DOI] [PubMed] [Google Scholar]
- Soboll S., Scholz R. Control of energy metabolism by glucagon and adrenaline in perfused rat liver. FEBS Lett. 1986 Sep 1;205(1):109–112. doi: 10.1016/0014-5793(86)80875-4. [DOI] [PubMed] [Google Scholar]
- Stanley P. E., Williams S. G. Use of the liquid scintillation spectrometer for determining adenosine triphosphate by the luciferase enzyme. Anal Biochem. 1969 Jun;29(3):381–392. doi: 10.1016/0003-2697(69)90323-6. [DOI] [PubMed] [Google Scholar]
- Strzelecki T., Strzelecka D., Koch C. D., LaNoue K. F. Sites of action of glucagon and other Ca2+ mobilizing hormones on the malate aspartate cycle. Arch Biochem Biophys. 1988 Jul;264(1):310–320. doi: 10.1016/0003-9861(88)90599-1. [DOI] [PubMed] [Google Scholar]
- Sugano T., Nishimura K., Sogabe N., Shiota M., Oyama N., Noda S., Ohta M. Ca2+-dependent activation of the malate-aspartate shuttle by norepinephrine and vasopressin in perfused rat liver. Arch Biochem Biophys. 1988 Jul;264(1):144–154. doi: 10.1016/0003-9861(88)90579-6. [DOI] [PubMed] [Google Scholar]
- Sugano T., Shiota M., Khono H., Shimada M., Oshino N. Effects of calcium ions on the activation of gluconeogenesis by norepinephrine in perfused rat liver. J Biochem. 1980 Feb;87(2):465–472. doi: 10.1093/oxfordjournals.jbchem.a132766. [DOI] [PubMed] [Google Scholar]
- Taylor W. M., Prpić V., Exton J. H., Bygrave F. L. Stable changes to calcium fluxes in mitochondria isolated from rat livers perfused with alpha-adrenergic agonists and with glucagon. Biochem J. 1980 May 15;188(2):443–450. doi: 10.1042/bj1880443. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas P. J., Gaspers L. D., Pharr C., Thomas J. A. Continuous measurement of mitochondrial pH gradients in isolated hepatocytes by difference ratio spectroscopy. Arch Biochem Biophys. 1991 Jul;288(1):250–260. doi: 10.1016/0003-9861(91)90192-l. [DOI] [PubMed] [Google Scholar]
- Whitehouse S., Cooper R. H., Randle P. J. Mechanism of activation of pyruvate dehydrogenase by dichloroacetate and other halogenated carboxylic acids. Biochem J. 1974 Sep;141(3):761–774. doi: 10.1042/bj1410761. [DOI] [PMC free article] [PubMed] [Google Scholar]