Ca2+-dependent permeability transition regulation in rat brain mitochondria by 2′,3′-cyclic nucleotides and 2′,3′- cyclic nucleotide 3′-phosphodiesterase

American Journal of Physiology - Cell Physiology

Volumn 296, Issue 6, 2009, Pages

  Azarashvili, Tamara ^a,b   Krestinina, Olga ^a,b   Galvita, Anastasia ^a   Grachev, Dmitry ^a,b   Baburina, Yulia ^b   Stricker, Rolf ^a   Evtodienko, Yuri ^b   Reiser, Georg ^a  

^a OTTO VON GUERICKE UNIVERSITY   (Germany)

^b INSTITUTE OF THEORETICAL AND EXPERIMENTAL BIOPHYSICS   (Russian Federation)

Author keywords

2 ,3 cyclic nucleotide 3 phosphodiesterase; Calcium transport; Oligodendrocyte mitochondria; Permeability transition

Indexed keywords

2',3' CYCLIC NUCLEOTIDE 3' PHOSPHODIESTERASE; 2',3' CYCLIC NUCLEOTIDE DERIVATIVE; CYCLOSPORIN A; NUCLEOTIDE DERIVATIVE; UNCLASSIFIED DRUG; 2',3' CYCLIC NADP; 2',3'-CYCLIC AMP; 2',3'-CYCLIC NADP; ADENINE NUCLEOTIDE; ADENOSINE 2',3' PHOSPHATE; CARRIER PROTEIN; CYCLOSPORIN; MITOCHONDRIAL PERMEABILITY TRANSITION PORE; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; SMALL INTERFERING RNA;

ANIMAL TISSUE; APOPTOSIS; ARTICLE; CALCIUM TRANSPORT; CONTROLLED STUDY; ENZYME ACTIVITY; HYDROLYSIS; MALE; MEMBRANE PERMEABILITY; MITOCHONDRION; MITOCHONDRION SWELLING; NONHUMAN; PRIORITY JOURNAL; RAT; ANIMAL; BRAIN; CALCIUM SIGNALING; CELL LINE; DRUG ANTAGONISM; DRUG EFFECT; ENZYMOLOGY; GENETICS; LIVER MITOCHONDRION; METABOLISM; MITOCHONDRIAL MEMBRANE POTENTIAL; OLIGODENDROGLIA; RNA INTERFERENCE; TIME; WISTAR RAT;

RATTUS;

2',3'-CYCLIC-NUCLEOTIDE PHOSPHODIESTERASES; ADENINE NUCLEOTIDES; ANIMALS; BRAIN; CALCIUM SIGNALING; CELL LINE; CYCLOSPORINE; MALE; MEMBRANE POTENTIAL, MITOCHONDRIAL; MITOCHONDRIA; MITOCHONDRIA, LIVER; MITOCHONDRIAL MEMBRANE TRANSPORT PROTEINS; MITOCHONDRIAL SWELLING; NADP; OLIGODENDROGLIA; RATS; RATS, WISTAR; RNA INTERFERENCE; RNA, SMALL INTERFERING; TIME FACTORS;

EID: 66749110373     PISSN: 03636143     EISSN: 15221563     Source Type: Journal    
DOI: 10.1152/ajpcell.00006.2009     Document Type: Article

References (43)

1. Agrawal HC, Sprinkle TJ, Agrawal D. 2′,3′-Cyclic nucleotide-3′-phosphodiesterase in the central nervous system is fatty-acylated by thioester linkage. J Biol Chem 265: 11849-11853, 1990. (Pubitemid 20219358)
2. Agrawal HC, Sprinkle TJ, Agrawal D. 2′,3′Cyclic nucleotide-3′-phosphodiesterase in peripheral nerve myelin is phosphorylated by a phorbol ester-sensitive protein kinase. Biochem Biophys Res Commun 170: 817-823, 1990. (Pubitemid 20249492)
3. Allen FW, Davis FF. A specific phosphodiesterase from beef pancreas. Biochim Biophys Acta 21: 14-17, 1956.
4. 2+-induced permeability transition pore opening in rat brain mitochondria. Cell Calcium 42: 27-39, 2007.
5. 2+-induced permeability transition pore control protein phosphorylation in rat brain mitochondria. Cell Calcium 34: 253-259, 2003.
6. Baines CP, Kaiser RA, Sheiko T, Craigen WJ, Molkentin JD. Voltage-dependent anion channels are dispensable for mitochondrial-dependent cell death. Nat Cell Biol 9: 550-555, 2007. (Pubitemid 46696536)
7. Bernardi P. Mitochondrial transport of cations: channels, exchangers, and permeability transition. Physiol Rev 79: 1127-1155, 1999. (Pubitemid 29473313)
8. Boneh A. Regulation of mitochondrial oxidative phosphorylation by second messenger-mediated signal transduction mechanisms. Cell Mol Life Sci 63: 1236-1248, 2006. (Pubitemid 43939010)
9. Bradbury JM, Thompson RJ. Photoaffinity labelling of central-nervous- system myelin. Evidence for an endogenous type I cyclic AMP-dependent kinase phosphorylating the larger subunit of 2′,3′-cyclic nucleotide 3′-phosphodiesterase. Biochem J 221: 361-368, 1984.
10. De Angelis DA, Braun PE. Isoprenylation of brain 2′,3′-cyclic nucleotide 3′-phosphodiesterase modulates cell morphology. J Neurosci Res 39:386-397, 1994. (Pubitemid 24348292)
11. + and is a causative event in the death of myocytes in postischemic reperfusion of the heart. J Biol Chem 276: 2571-2575, 2001.
12. Dreiling CE, Schilling RJ, Reitz RC. 2′,3′-Cyclic nucleotide 3′-phosphohydrolase in rat liver mitochondrial membranes. Biochim Biophys Acta 640: 114-120, 1981.
13. Drummond GI, Iyer NT, Keith J. Hydrolysis of ribonucleoside 2′,3′-cyclic phosphates by a diesterase from brain. J Biol Chem 237: 3535-3539, 1962.
14. Giulian D, Iwanij V, Dean G, Drummond RJ. Localization of 2′,3′-cyclic nucleotide-3′-phosphohydrolase within the vertebrate retina. Brain Res 265: 217-225, 1983.
15. Giulian D, Moore S. Identification of 2′:3′-cyclic nucleotide 3′-phosphodiesterase in the vertebrate retina. J Biol Chem 255: 5993-5995, 1980. (Pubitemid 10014202)
16. Gravel M, DeAngelis D, Braun PE. Molecular cloning and characterization of rat brain 2′,3′-cyclic nucleotide 3′-phosphodiesterase isoform 2. J Neurosci Res 38: 243-247, 1994. (Pubitemid 24189629)
17. Gravel M, Robert F, Kottis V, Gallouzi IE, Pelletier J, Braun PE. 2′,3′-Cyclic nucleotide 3′-phosphodiesterase: a novel RNA-binding protein that inhibits protein synthesis. J Neurosci Res 87: 1069-1079, 2009.
18. Halestrap AP. Calcium, mitochondria and reperfusion injury: a pore way to die. Biochem Soc Trans 34: 232-237, 2006.
19. Halestrap AP, McStay GP, Clarke SJ. The permeability transition pore complex: another view. Biochimie 84: 153-166, 2002. (Pubitemid 34936515)
20. Heaton PA, Eckstein F. Diastereomeric specificity of 2′,3′- cyclic nucleotide 3′-phosphodiesterase. Nucleic Acids Res 24: 850-853, 1996. (Pubitemid 26076189)
21. Juhaszova M, Wang S, Zorov DB, Nuss HB, Gleichmann M, Mattson MP, Sollott SJ. The identity and regulation of the mitochondrial permeability transition pore: where the known meets the unknown. Ann N Y Acad Sci 1123: 197-212, 2008.
22. Keppetipola N, Shuman S. Characterization of the 2′,3′ cyclic phosphodiesterase activities of Clostridium thermocellum polynucleotide kinase-phosphatase and bacteriophage lambda phosphatase. Nucleic Acids Res 35: 7721-7732, 2007.
23. Kurihara T, Nishizawa Y, Takahashi Y, Odani S. Chemical, immunological and catalytic properties of 2′:3′-cyclic nucleotide 3′-phosphodiesterase purified from brain white matter. Biochem J 195: 153-157, 1981.
24. Lee J, O'Neill RC, Park MW, Gravel M, Braun PE. Mitochondrial localization of CNP2 is regulated by phosphorylation of the N-terminal targeting signal by PKC: implications of a mitochondrial function for CNP2 in glial and non-glial cells. Mol Cell Neurosci 31: 446-462, 2006.
25. Leissring MA, Farris W, Wu X, Christodoulou DC, Haigis MC, Guarente L, Selkoe DJ. Alternative translation initiation generates a novel isoform of insulin-degrading enzyme targeted to mitochondria. Biochem J 383: 439-446, 2004. (Pubitemid 39546113)
26. Low RL. Mitochondrial endonuclease G function in apoptosis and mtDNA metabolism: a historical perspective. Mitochondrion 2: 225-236, 2003. (Pubitemid 36347777)
27. McFerran B, Burgoyne R. 2′,3′-Cyclic nucleotide 3′-phosphodiesterase is associated with mitochondria in diverse adrenal cell types. J Cell Sci 110: 2979-2985, 1997. (Pubitemid 28005813)
28. O'Neill RC, Minuk J, Cox ME, Braun PE, Gravel M. CNP2 mRNA directs synthesis of both CNP1 and CNP2 polypeptides. J Neurosci Res 50: 248-257, 1997.
29. Papa S, De Rasmo D, Scacco S, Signorile A, Technikova-Dobrova Z, Palmisano G, Sardanelli AM, Papa F, Panelli D, Scaringi R, Santeramo A. Mammalian complex I: a regulable and vulnerable pacemaker in mitochondrial respiratory function. Biochim Biophys Acta 1777: 719-728, 2008.
30. Reiser G, Kunzelmann U, Steinhilber G, Binmöller FJ. Generation of a monoclonal antibody against the myelin protein CNP (2′,3′-cyclic nucleotide 3′-phosphodiesterase) suitable for biochemical and for immunohistochemical investigations of CNP. Neurochem Res 19: 1479-1485, 1994. (Pubitemid 24370063)
31. Rice JE, Lindsay JG. Subcellular fractionation of mitochondria. In: Subcellular Fractionation: A Practical Approach, edited by Graham JM and Rickwood D. Oxford, UK: IRL, 1997, p. 107-142.
32. Richter-Landsberg C, Heinrich M. OLN-93: a new permanent oligodendroglia cell line derived from primary rat brain glial cultures. J Neurosci Res 45: 161-173, 1996. (Pubitemid 26257317)
33. Schwer B, Aronova A, Ramirez A, Braun P, Shuman S. Mammalian 2′,3′ cyclic nucleotide phosphodiesterase (CNP) can function as a tRNA splicing enzyme in vivo. RNA 14: 204-210, 2008.
34. Sims NR. Rapid isolation of metabolically active mitochondria from rat brain and subregions using Percoll density gradient centrifugation. J Neurochem 55: 698-707, 1990. (Pubitemid 120021648)
35. Sogin DC. 2′,3′-Cyclic NADP as a substrate for 2′,3′-cyclic nucleotide 3′-phosphohydrolase. J Neurochem 27: 1333-1337, 1976.
36. Sprinkle TJ. 2′,3′-Cyclic nucleotide 3′- phosphodiesterase, an oligodendrocyte-Schwann cell and myelin-associated enzyme of the nervous system. Crit Rev Neurobiol 4: 235-301, 1989. (Pubitemid 19068704)
37. Sprinkle TJ, Tippins RB, Kestler DP. Inhibition of bovine and human brain 2′:3′-cyclic nucleotide 3′-phosphodiesterase by heparin and polyribonucleotides and evidence for an associated 5′-polynucleotide kinase activity. Biochem Biophys Res Commun 145: 686-691, 1987.
38. Stricker R, Lottspeich F, Reiser G. The myelin protein CNP (2′,3′-cyclic nucleotide 3′-phosphodiesterase): immunoaffinity purification of CNP from pig and rat brain using a monoclonal antibody and phosphorylation of CNP by cyclic nucleotide-dependent protein kinases. Biol Chem Hoppe Seyler 375: 205-209, 1994. (Pubitemid 2064586)
39. Vogel US, Thompson RJ. Molecular structure, localization, and possible functions of the myelin-associated enzyme 2′,3′-cyclic nucleotide 3′-phosphodiesterase. J Neurochem 50: 1667-1677, 1988. (Pubitemid 18140716)
40. Weissbarth S, Maker HS, Raes I, Brannan TS, Lapin EP, Lehrer GM. The activity of 2′,3′-cyclic nucleotide 3′-phosphodiesterase in rat tissues. J Neurochem 37: 677-680, 1981. (Pubitemid 11016900)
41. Zago EB, Castilho RF, Vercesi AE. The redox state of endogenous pyridine nucleotides can determine both the degree of mitochondrial oxidative stress and the solute selectivity of the permeability transition pore. FEBS Lett 478: 29-33, 2000. (Pubitemid 30462253)
42. Zippin JH, Chen Y, Nahirney P, Kamenetsky M, Wuttke MS, Fischman DA, Levin LR, Buck J. Compartmentalization of bicarbonatesensitive adenylyl cyclase in distinct signaling microdomains. FASEB J 17: 82-84, 2003.
43. Zoratti M, Szabo I, De Marchi U. Mitochondrial permeability transitions: how many doors to the house? Biochim Biophys Acta 1706: 40-52, 2005.