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2002 | 07 | 4 |

Tytuł artykułu

The influence of membrane lipid metabolites on lymphocyte potassium channel activity

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
In the present study, the whole-cell patch-clamp technique was applied to elucidate modulatory effects of high-density lipoproteins (HDL), sphingosine (SPH), sphingosine-l-phosphate (SPP), lysophosphatidic acid (LPA) and sphingosyl- phosphorylcholine (SPC) on the activity of Kvl.3 channels in human T lymphocytes (TL). Obtained data provide evidence that application of SPC at micromolar concentrations shifts the channel activation midpoint by about 20 mV towards positive membrane potentials. This effect occurs in a concentration-dependent manner and is saturated at SPC concentrations higher than 10 µM. The shift of channel activation midpoint is accompanied by a pronounced slowing of the activation kinetics. The modulatory effect of SPC is clearly voltage-dependent, being most potent at -20 mV and least potent at +60 mV. The steady-state inactivation curve is also shifted by about 20 mV towards positive membrane potentials. The kinetics of channel inactivation and deactivation (closure) remain unaffected upon SPC treatment. In contrast, application of HDL (250 µg/ml), SPH (50 and 100 µM), SPP (10 µM) and LPA (10 and 36 µM) does not exert any modulatory effect on the channel activity. The effect of SPC on Kvl.3 channel gating resembles the effect exerted by extracellular zinc at the concentration of 10 µM. It is concluded that the effect of SPC is specific and may be due to the presence of a choline residue in SPC molecules. The possible mechanism and the physiological significance of this modulatory effect on Kvl.3 channels are discussed.

Wydawca

-

Rocznik

Tom

07

Numer

4

Opis fizyczny

p.1095-1109,fig.,ref.

Twórcy

autor
  • Department of Biophysics, Wroclaw Medical University, Chalubinskiego 10, 50-368 Wroclaw, Poland
autor
  • Department of Biophysics, Wroclaw Medical University, Chalubinskiego 10, 50-368 Wroclaw, Poland
  • Department and Clinic of Haematology and Oncology, Wroclaw Medical University, Pasteura 4, 50-367 Wroclaw, Poland

Bibliografia

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  • 2. Mattie, M., Brooker, G. and Spiegel, S. Sphingosine-1-phosphate, a putative second messenger mobilizes calcium from internal stores via an inositol triphosphate-independent pathway. J. Biol. Chem. 269 (1994) 3181-3188.
  • 3. Kim, S., Lakhani, V., Costa, D., Sharara, A., Fitz, G., Huang, L., Peters, K. and Kindman, L. Sphingolipid-gated Ca2+ release from intracellular stores of endothelial cells is mediated by a novel Ca2+ permeable channel. J. Biol. Chem. 270 (1995) 5266-5269.
  • 4. Koppen van, Ch., Meyer zu Heringdorf, D., Laser, K., Zhang, Ch., Jakobs, K., Bünemann, M. and Pott L. Activation of high affinity G protein-coupled plasma membrane receptor by sphingosine-1-phosphate. J. Biol. Chem. 271 (1996) 2082-2087.
  • 5. Bünemann M., Brandts, B., Meyer zu Heringdorf, D., Koppen van, Ch., Jakobs K. and, Pott L. Activation of muscarinic K+ current in guinea-pig atrial myocytes by sphingosine-1-phosphate. J. Physiol. (Lond.) 489 (1995) 701-707.
  • 6. Bünemann, M., Liliom, K., Brandts, B., Pott, L., Tseng, J., Desiderio, D., Sun, G., Miller, D. and Tigyi, G. A novel membrane receptor with high affinity for lysosphingomyelin and sphingosine 1-phosphate in atrial myocytes. EMBO J. 15 (1996) 5527-5534.
  • 7. Jürgens, G., Xu, Q., Huber, L., Böck, G., Howanietz, Wick, G. and Traill, K. Promotion of lymphocyte growth by high density lipoproteins (HDL). J. Biol. Chem. 264 (1989) 8549-8556.
  • 8. Xu, Q., Bühler, E., Steinmetz, A., Schönitzer, D., Böck, G., Jürgens, G. and Wick, G. A high-density-lipoprotein receptor appears to mediate the transfer of essential fatty acids from high-density lipoprotein to lymphocytes. Biochem. J. 287 (1992) 395-401.
  • 9. Xu, Y., Casey, G. and Mills, G. Effect of lysophospholipids on signalling in the human Jurkat T cell line. J. Cell. Physiol. 163 (1995) 441-450.
  • 10. Breittmayer, J., Bernard, A. and Aussel, C. Regulation by sphingomyelinase and sphingosine of Ca2+ signals elicited by CD3 monoclonal antibody, thapsigargin or ionomycin in the Jurkat T cell line. J. Biol. Chem. 269 (1994) 5054-5058.
  • 11. Cuvillier, O., Rosenthal, D., Smulson, M. and Spiegel, S. Sphingosine-1- phosphate inhibits activation of caspases that cleave poly (ADP-ribose) polymerase and lamins during Fas- and ceramide-mediated apoptosis in Jurkat T Lymphocytes. J. Biol. Chem. 273 (1998) 2910-2916.
  • 12. Lewis, R. S. and Cahalan, M. D. Potassium and calcium channels in lymphocytes. Annu. Rev. Immunol. 13 (1995) 623-653.
  • 13. Teisseyre, A. Funkcja kanałów potasowych napięciowozależnych w limfocytach T w stanie fizjologii i patologii. Post. Hig. Med. Dośw. 53 (1999) 383-397.
  • 14. Teisseyre, A. The patch-clamp technique and its applications in investigations of the properties of human T lymphocyte potassium channels. Cell. Mol. Biol. Lett. 6 (2001) 93-105.
  • 15. Teisseyre, A., Michalak, K. and Kuliszkiewicz Janus, M. The modulation of lymphocyte potassium channels by membrane lipid metabolites. Cell. Mol. Biol. Lett. 7 (2002) Suppl. 224.
  • 16. Teisseyre, A. Technika patch-clamp w badaniach modulacji aktywności kanałów potasowych w limfocytach T. Post. Hig. Med. Dośw. 56 (2002) 393-399.
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  • 18. Hamill, O. P., Marty, A., Nehe,r E., Sakmann, B. and Sigworth, F. J. Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pfluegers Arch. 391 (1981) 85-100.
  • 19. Teisseyre, A. and Mozrzymas, J. W. Inhibition of the Activity of T Lymphocyte Kvl.3 Channels by Extracellular Zinc. Biochem. Pharmacol. 64 (2002) 595-607.
  • 20. Teisseyre, A. Regulacja funkcji kanałów potasowych w limfocytach T przez wewnątrzkomórkowe wtórne przekaźniki na przykładzie wapnia, cyklicznego AMP i związków lipidowych. Post. Hig. Med. Dośw. 54 (2000) 381-390.
  • 21. Gilly, F. and Armstrong, C. M. Divalent cations and the activation kinetics of potassium channels in squid giant axons. J. Gen. Physiol. 79 (1982) 965- 996.
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Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

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