Nuclear targeting of FBPase in HL-1 cells is controlled by beta-1 adrenergic receptor-activated Gs protein signaling cascade

Biochimica et Biophysica Acta - Molecular Cell Research

Volumn 1793, Issue 5, 2009, Pages 871-877

  Gizak, Agnieszka ^a   Zarzycki, Marek ^a   Rakus, Dariusz ^a  

^a UNIVERSITY OF WROC AW   (Poland)

Author keywords

HL 1 cell; Muscle FBPase; Norepinephrine; Phosphoinositide 3 kinase; Protein kinase A

Indexed keywords

ADENYLATE CYCLASE; BETA 1 ADRENERGIC RECEPTOR; CYCLIC AMP DEPENDENT PROTEIN KINASE; FRUCTOSE BISPHOSPHATASE; ISOPRENALINE; METOPROLOL; STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN;

ARTICLE; CELL COMPARTMENTALIZATION; CELL STIMULATION; CONTROLLED STUDY; CYTOPLASM; ENZYME ACTIVITY; ENZYME REGULATION; HEART MUSCLE CELL; HUMAN; HUMAN CELL; NUCLEAR IMPORT; PRIORITY JOURNAL; PROTEIN TARGETING; PROTEIN TRANSPORT; SIGNAL TRANSDUCTION;

ACTIVE TRANSPORT, CELL NUCLEUS; ADENYLATE CYCLASE; ADRENERGIC ALPHA-AGONISTS; ADRENERGIC BETA-AGONISTS; ADRENERGIC BETA-ANTAGONISTS; ANIMALS; CELL LINE; CELL NUCLEUS; CULTURE MEDIA; CYCLIC AMP-DEPENDENT PROTEIN KINASES; FORSKOLIN; FRUCTOSE-BISPHOSPHATASE; GTP-BINDING PROTEIN ALPHA SUBUNITS, GS; ISOPROTERENOL; METOPROLOL; MICE; MYOCYTES, CARDIAC; NOREPINEPHRINE; RECEPTORS, ADRENERGIC, BETA-1; SECOND MESSENGER SYSTEMS;

EID: 67349230151     PISSN: 01674889     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamcr.2009.02.005     Document Type: Article

References (33)

1. Gomori G. Hexosediphosphatase. J. Biol. Chem. 148 (1943) 139-149
2. Tejwani G.A. Regulation of fructose-bisphosphatase activity. Adv. Enzymol. Relat. Areas Mol. Biol. 54 (1983) 121-194
3. Al-Robaiy S., and Eschrich K. Rat muscle fructose-1,6-bisphosphatase: cloning of the cDNA, expression of the recombinant enzyme, and expression analysis in different tissues. Biol. Chem. 380 (1999) 1079-1085
4. Tillmann H., Bernhard D., and Eschrich K. Fructose-1,6-bisphosphatase genes in animals. Gene 291 (2002) 57-66
5. Gleeson T.T. Post-exercise lactate metabolism: a comparative review of sites, pathways, and regulation. Annu. Rev. Physiol. 58 (1996) 565-581
6. Rakus D., and Dzugaj A. Muscle aldolase decreases muscle FBPase sensitivity toward AMP inhibition. Biochem. Biophys. Res. Commun. 275 (2000) 611-616
7. Gizak A., Majkowski M., Dus D., and Dzugaj A. Calcium inhibits muscle FBPase and affects its intracellular localization in cardiomyocytes. FEBS Lett. 576 (2004) 445-448
8. Mamczur P., Rakus D., Gizak A., Dus D., and Dzugaj A. The effect of calcium ions on subcellular localization of aldolase-FBPase complex in skeletal muscle. FEBS Lett. 579 (2005) 1607-1612
9. Zarzycki M., Maciaszczyk E., and Dzugaj A. Glu 69 is essential for the high sensitivity of muscle fructose-1,6-bisphosphatase inhibition by calcium ions. FEBS Lett. 581 (2007) 1347-1350
10. Gizak A., Maciaszczyk E., Eschrich K., Dzugaj A., and Rakus D. Evolutionary conserved N-terminal region of muscle FBPase regulates its activity and the interaction with aldolase. Proteins Struct. Funct. Bioinform. 72 (2008) 209-216
11. Löffler T., Al.-Robaiy S., Bigl M., Eschrich K., and Schliebs R. Expression of fructose-1,6-bisphosphatase mRNA isoforms in normal and basal forebrain cholinergic lesioned rat brain. Int. J. Dev. Neurosci. 19 (2001) 279-285
12. Gizak A., and Dzugaj A. FBPase is in the nuclei of cardiomyocytes. FEBS Lett. 539 (2003) 51-55
13. Gizak A., Rakus D., and Dzugaj A. Nuclear localization of fructose 1,6-bisphosphatase in smooth muscle cells. J. Mol. Histol. 36 (2005) 243-248
14. Gizak A., Wrobel E., Moraczewski J., and Dzugaj A. Changes in subcellular localization of fructose 1,6-bisphosphatase during differentiation of isolated muscle satellite cells. FEBS Lett. 580 (2006) 4042-4046
15. Jeffery C.J. Multifunctional proteins: examples of gene sharing. Ann. Med. 35 (2003) 28-35
16. Yáñez A.J., Garcia-Rocha M., Bertinat R., Droppelmann C., Concha I.I., Guinovart J.J., and Slebe J.C. Subcellular localization of liver FBPase is modulated by metabolic conditions. FEBS Lett. 577 (2004) 154-158
17. Claycomb W.C., Lanson Jr. N.A., Stallworth B.S., Egeland D.B., Delcarpio J.B., Bahinski A., and Izzo Jr. N.J. HL-1 cells: a cardiac muscle cell line that contracts and retains phenotypic characteristics of the adult cardiomyocyte. Proc. Natl. Acad. Sci. 95 (1996) 2979-2984
18. White S.M., Constantin P.E., and Claycomb W.C. Cardiac physiology at the cellular level: use of cultured HL-1 cardiomyocytes for studies of cardiac muscle cell structure and function. Am. J. Physiol. Heart Circ. Physiol. 286 (2004) H823-H829
19. Towbin H., Staehelin T., and Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc. Natl. Acad. Sci. 76 (1979) 4350-4354
20. Nishi K., Yoshida M., Fujiwara D., Nishikawa M., Horinouchi S., and Beppu T. Leptomycin B targets a regulatory cascade of crm1, a fission yeast nuclear protein, involved in control of higher order chromosome structure and gene expression. J. Biol. Chem. 269 (1994) 6320-6324
21. Filipeanu C.M., Zhou F., Lam M.L., Kerut K.E., Claycomb W.C., and Wu G. Enhancement of the recycling and activation of beta-adrenergic receptor by Rab4 GTPase in cardiac myocytes. J. Biol. Chem. 281 (2006) 11097-11103
22. Whalen E.J., and Lewis S.J. In vivo evidence that isoproterenol may increase heart rate in the rat by mechanisms in addition to activation of cardiac β1- or β2-adrenoceptors. Eur. J. Pharmacol. 382 (1999) 207-210
23. Galandrin S., and Bouvier M. Distinct signaling profiles of beta1 and beta2 adrenergic receptor ligands toward adenylyl cyclase and mitogen-activated protein kinase reveals the pluridimensionality of efficacy. Mol. Pharmacol. 70 (2006) 1575-1584
24. Kuschel M., Zhou Y.Y., Cheng H., Zhang S.J., Chen Y., Lakatta E.G., and Xiao R.P. G(i) protein-mediated functional compartmentalization of cardiac beta(2)-adrenergic signaling. J. Biol. Chem. 274 (1999) 22048-22052
25. Cass L.A., Summers S.A., Prendergast G.V., Backer J.M., Birnbaum M.J., and Meinkoth J.L. Protein kinase A-dependent and -independent signaling pathways contribute to cyclic AMP-stimulated proliferation. Mol. Cell. Biol. 19 (1999) 5882-5891
26. Misra U.K., and Pizzo S.V. Coordinate regulation of forskolin-induced cellular proliferation in macrophages by protein kinase A/cAMP-response element-binding protein (CREB) and Epac1-Rap1 signaling: effects of silencing CREB gene expression on Akt activation. J. Biol. Chem. 280 (2005) 38276-38289
27. Rakus D., Zarzycki M., and Dzugaj A. Rabbit muscle fructose-1,6-bisphosphatase is phosphorylatedin vivo. Acta Biochim. Pol. 50 (2003) 115-121
28. Zou Y., Kamuro I., Yamazaki T., Kudoh S., Uozumi H., Kadowaki T., and Yazaki Y. Both Gs and Gi proteins are critically involved in isoproterenol-induced cardiomyocyte hipertrophy. J. Biol. Chem. 274 (1999) 9760-9770
29. Leicht M., Greipel N., and Zimmer H. Comitogenic effect of catecholamines on rat cardiac fibroblasts in culture. Cardiovasc. Res. 48 (2000) 274-284
30. Singh K., Xiao L., Remondino A., Sawyer D.B., and Colucci W.S. Adrenergic regulation of cardiac myocyte apoptosis. J. Cell. Physiol. 189 (2001) 257-265
31. Kwak H.J., Park K.M., Choi H.E., Chung K.S., Lim H.J., and Park H.Y. PDE4 inhibitor, roflumilast protects cardiomyocytes against NO-induced apoptosis via activation of PKA and Epac dual pathways. Cell. Signal. 20 (2008) 803-814
32. Kitanovic A., and Wölfl S. Fructose-1,6-bisphosphatase mediates cellular responses to DNA damage and aging in Saccharomyces cerevisiae. Mutat. Res. 594 (2006) 135-147
33. Voehringer D.W., Hirschberg D.L., Xiao J., Lu Q., Roederer M., Lock C.B., Herzenberg L.A., Steinman L., and Herzenberg L.A. Gene microarray identification of redox and mitochondrial elements that control resistance or sensitivity to apoptosis. Proc. Natl. Acad. Sci. 97 (2000) 2680-2685