Calcium influx into phospholipid vesicles caused by dynorphin neuropeptides

Biochimica et Biophysica Acta - Biomembranes

Volumn 1778, Issue 5, 2008, Pages 1267-1273

  Hugonin, Loïc ^a   Vukojević, Vladana ^b   Bakalkin, Georgy ^c   Gräslund, Astrid ^a  

^a STOCKHOLM UNIVERSITY   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

^c UPPSALA UNIVERSITY   (Sweden)

Author keywords

Calcium influx; Cell penetrating peptides; Dynorphin; Energy transfer; Fluorescence; Phospholipid membranes; Unilamellar vesicles

Indexed keywords

AMPHOLYTE; BIG DYNORPHIN; CALCEIN; CALCIUM; CELL PENETRATING PEPTIDE; DYNORPHIN; DYNORPHIN A; DYNORPHIN B; DYNORPHIN[1-13]; KAPPA OPIATE RECEPTOR; LIGAND; NEUROPEPTIDE; PENETRATIN; PHOSPHOLIPID;

AMINO ACID SEQUENCE; ARTICLE; CALCIUM TRANSPORT; ELECTRICITY; ENERGY TRANSFER; FLUORESCENCE; FLUORESCENCE RESONANCE ENERGY TRANSFER; HYDROPHOBICITY; PHOSPHOLIPID VESICLE; PRIORITY JOURNAL; PROTEIN TRANSPORT;

AMINO ACID SEQUENCE; CALCIUM; DYNORPHINS; FLUORESCENCE; FLUORESCENCE RESONANCE ENERGY TRANSFER; ION TRANSPORT; MOLECULAR SEQUENCE DATA; PHOSPHOLIPIDS;

EID: 43049125756     PISSN: 00052736     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbamem.2008.02.003     Document Type: Article

References (48)

1. Fallon J.H., and Leslie F.M. Distribution of dynorphin and enkephalin peptides in the rat brain. J. Comp. Neurol. 249 (1986) 293-336
2. Khachaturian H., Watson S.J., Lewis M.E., Coy D., Goldstein A., and Akil H. Dynorphin immunocytochemistry in the rat central nervous system. Peptides 3 (1982) 941-954
3. Mansour A., Fox C.A., Burke S., Meng F., Thompson R.C., Akil H., and Watson S.J. Mu, delta, and κ-opioid receptor mRNA expression in the rat CNS: an in situ hybridization study. J. Comp. Neurol. 350 (1994) 412-438
4. Pierce J.P., Kurucz O.S., and Milner T.A. Morphometry of a peptidergic transmitter system: dynorphin B-like immunoreactivity in the rat hippocampal mossy fiber pathway before and after seizures. Hippocampus 9 (1999) 255-276
5. Van Bockstaele E.J., Sesack S.R., and Pickel V.M. Dynorphin-immunoreactive terminals in the rat nucleus accumbens: cellular sites for modulation of target neurons and interactions with catecholamine afferents. J. Comp. Neurol. 341 (1994) 1-15
6. Fischli W., Goldstein A., Hunkapiller M.W., and Hood L.E. Isolation and amino acid sequence analysis of a 4000-dalton dynorphin from porcine pituitary. Proc. Natl. Acad. Sci. U. S. A. 79 (1982) 5435-5437
7. Xie G.X., and Goldstein A. Characterization of big dynorphins from rat brain and spinal cord. J. Neurosci. 7 (1987) 2049-2055
8. Day R., and Akil H. The posttranslational processing of prodynorphin in the rat anterior pituitary. Endocrinology 124 (1989) 2392-2405
9. Hauser K.F., Aldrich J.V., Anderson K.J., Bakalkin G., Christie M.J., Hall E.D., Knapp P.E., Scheff S.W., Singh I.N., Vissel B., Woods A.S., Yakovleva T., and Shippenberg T.S. Pathobiology of dynorphins in trauma and disease. Front. Biosci. 10 (2005) 216-235
10. Costigan M., and Woolf C.J. No DREAM, No pain. Closing the spinal gate. Cell 108 (2002) 297-300
11. De Vries T.J., and Shippenberg T.S. Neural systems underlying opiate addiction. J. Neurosci. 22 (2002) 3321-3325
12. Kreek M.J., LaForge K.S., and Butelman E. Pharmacotherapy of addictions. Nat. Rev. Drug Discov. 1 (2002) 710-726
13. Kuzmin A., Madjid N., Terenius L., Ogren S.O., and Bakalkin G. Big dynorphin, a prodynorphin-derived peptide produces NMDA receptor-mediated effects on memory, anxiolytic-like and locomotor behavior in mice. Neuropsychopharmacology 31 (2006) 1928-1937
14. Trujillo K.A., and Akil H. Opioid and non-opioid behavioral actions of dynorphin A and the dynorphin analogue DAKLI. NIDA Res. Monogr. 105 (1991) 397-398
15. Vanderah T.W., Laughlin T., Lashbrook J.M., Nichols M.L., Wilcox G.L., Ossipov M.H., Malan Jr. T.P., and Porreca F. Single intrathecal injections of dynorphin A or des-Tyr-dynorphins produce long-lasting allodynia in rats: blockade by MK-801 but not naloxone. Pain 68 (1996) 275-281
16. Wang Z., Gardell L.R., Ossipov M.H., Vanderah T.W., Brennan M.B., Hochgeschwender U., Hruby V.J., Malan Jr. T.P., Lai J., and Porreca F. Pronociceptive actions of dynorphin maintain chronic neuropathic pain. J. Neurosci. 21 (2001) 1779-1786
17. Xu M., Petraschka M., McLaughlin J.P., Westenbroek R.E., Caron M.G., Lefkowitz R.J., Czyzyk T.A., Pintar J.E., Terman G.W., and Chavkin C. Neuropathic pain activates the endogenous kappa opioid system in mouse spinal cord and induces opioid receptor tolerance. J. Neurosci. 24 (2004) 4576-4584
18. Tan-No K., Esashi A., Nakagawasai O., Niijima F., Tadano T., Sakurada C., Sakurada T., Bakalkin G., Terenius L., and Kisara K. Intrathecally administered big dynorphin, a prodynorphin-derived peptide, produces nociceptive behavior through an N-methyl-d-aspartate receptor mechanism. Brain Res. 952 (2002) 7-14
19. Tan-No K., Takahashi H., Nakagawasai O., Niijima F., Sato T., Sato S., Sakurada S., Marinova Z., Yakovleva T., Bakalkin G., Terenius L., and Tadano T. A pronociceptive role of dynorphins in uninjured animals: nociceptive effects of N-ethylmaleimide mediated through inhibition of degradation of endogenous dynorphins. Pain 113 (2005) 301-309
20. Walker J.M., Moises H.C., Coy D.H., Baldrighi G., and Akil H. Nonopiate effects of dynorphin and des-Tyr-dynorphin. Science 218 (1982) 1136-1138
21. Singh I.N., Goody R.J., Goebel S.M., Martin K.M., Knapp P.E., Marinova Z., Hirschberg D., Yakovleva T., Bergman T., Bakalkin G., and Hauser K.F. Dynorphin A (1-17) induces apoptosis in striatal neurons in vitro through alpha-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate receptor-mediated cytochrome c release and caspase-3 activation. Neuroscience 122 (2003) 1013-1023
22. Tang Q., Lynch R.M., Porreca F., and Lai J. Dynorphin A elicits an increase in intracellular calcium in cultured neurons via a non-opioid, non-NMDA mechanism. J. Neurophysiol. 83 (2000) 2610-2615
23. Marinova Z., Vukojević V., Surcheva S., Yakovleva T., Cebers G., Pasikova N., Usynin I., Hugonin L., Fang W., Hallberg M., Hirschberg D., Bergman T., Langel Ü., Hauser K.F., Pramanik A., Aldrich J.V., Gräslund A., Terenius L., and Bakalkin G. Translocation of dynorphin neuropeptides across the plasma membrane. A putative mechanism of signal transmission. J. Biol. Chem. 280 (2005) 26360-26370
24. Hugonin L., Vukojevic V., Bakalkin G., and Gräslund A. Membrane leakage induced by dynorphins. FEBS Lett. 580 (2006) 3201-3205
25. Sato K., Horibe K., Amano K., Mitusi-Saito M., Hori M., Matsunaga S., Fusetani N., Ozaki H., and Karaki H. Membrane permeabilization induced by discodermin A, a novel marine bioactive peptide. Toxicon 39 (2001) 259-264
26. Demuro A., Mina E., Kayed R., Milton S.C., Parker I., and Glabe C.G. Calcium dysregulation and membrane disruption as a ubiquitous neurotoxic mechanism of soluble amyloid oligomers. J. Biol. Chem. 280 (2005) 17294-17300
27. Gill S.C., and von Hippel P.H. Calculation of protein extinction coefficients from amino acid sequence data. Anal. Biochem. 182 (1989) 319-326
28. Grynkiewicz G., Poenie M., and Tsien R.Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J. Biol. Chem. 260 (1985) 3440-3450
29. Matsuzaki K., Murase O., Fujii N., and Miyajima K. Translocation of a channel-forming antimicrobial peptide, magainin 2, across lipid bilayers by forming a pore. Biochemistry 34 (1995) 6521-6526
30. Matsuzaki K., Yoneyama S., Murase O., and Miyajima K. Transbilayer transport of ions and lipids coupled with mastoparan X translocation. Biochemistry 35 (1996) 8450-8456
31. Matsuzaki K., Yoneyama S., and Miyajima K. Pore formation and translocation of melittin. Biophys. J. 73 (1997) 831-838
32. Drin G., Déméné H., Temsamani J., and Brasseur R. Translocation of the pAntp peptide and its amphipathic analogue AP-2AL. Biochemistry 40 (2001) 1824-1834
33. Heidelberger R., Heinemann C., Neher E., and Matthews G. Calcium dependence of the rate of exocytosis in a synaptic terminal. Nature 371 (1994) 513-515
34. Joborn C., Hetta J., Niklasson F., Rastad J., Wide L., Agren H., Akerström G., and Ljunghall S. Cerebrospinal fluid calcium, parathyroid hormone, and monoamine and purine metabolites and the blood-brain barrier function in primary hyperparathyroidism. Psychoneuroendocrinology 16 (1991) 311-322
35. Parekh A.B. Store-operated Ca2+ entry: dynamic interplay between endoplasmic reticulum, mitochondria and plasma membrane. J. Physiol. 547 (2003) 333-348
36. 2+ microdomains. Cell Calcium 40 (2006) 527-537
37. Nicholls D.G. Mitochondria and calcium signaling. Cell Calcium 38 (2005) 311-317
38. Gunter T.E., and Pfeiffer D.R. Mechanisms by which mitochondria transport calcium. Am. J. Physiol. 258 (1990) C755-C786
39. Pokhilko A.V., Ataullakhanov F.I., and Holmuhamedov E.L. Mathematical model of mitochondrial ionic homeostasis: three modes of Ca2+, transport. J. Theor. Biol. 243 (2006) 152-169
40. Kyte J., and Doolittle R.F. A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 157 (1982) 105-132
41. Sukharev S.I., Blount P., Martinac B., Blattner F.R., and Kung C. A large-conductance mechanosensitive channel in E. coli encoded by mscL alone. Nature 368 (1998) 265-268
42. Gudi S., Nolan J.P., and Frangos J.A. Modulation of GTPase activity of G proteins by fluid shear stress and phospholipid composition. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 2515-2519
43. Knudsen H.L., and Frangos J.A. Role of cytoskeleton in shear stress-induced endothelial nitric oxide production. Am. J. Physiol. 42 (1997) H347-H355
44. Lee A.G. How lipids affect the activities of integral membrane proteins. Biochim. Biophys. Acta 1666 (2004) 62-87
45. Lai J., Luo M.C., Chen Q., Ma S., Gardell L.R., Ossipov M.H., and Porreca F. Dynorphin A activates bradykinin receptors to maintain neuropathic pain. Nat. Neurosci. 9 (2006) 1534-1540
46. Chachisvilis M., Zhang Y.L., and Frangos J.A. G protein-coupled receptors sense fluid shear stress in endothelial cells. Proc. Natl. Acad. Sci. U. S. A. 103 (2006) 15463-15468
47. Lind J., Gräslund A., and Mäler L. Membrane interactions of dynorphins. Biochemistry 45 (2006) 15931-15940
48. Magzoub M., Oglecka K., Pramanik A., Eriksson L.E.G., and Gräslund A. Membrane perturbation effects of peptides derived from the N-termini of unprocessed prion proteins. Biochim. Biophys. Acta 1716 (2005) 126-136