Inhibition of TRP3 channels by lanthanides -: Block from the cytosolic side of the plasma membrane

被引:113
作者
Halaszovich, CR [1 ]
Zitt, C [1 ]
Jüngling, E [1 ]
Lückhoff, A [1 ]
机构
[1] Univ Klinikum Aachen, Rhein Westfal TH Aachen, Inst Physiol, D-52074 Aachen, Germany
关键词
D O I
10.1074/jbc.M007010200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The lanthanide ions La3+ and Gd3+ block Ca2+-permeable cation channels and have been used as important tools to characterize channels of the transient receptor potential (TRP) family, However, widely different concentrations of La3+ and Gd3+ have reportedly been required for block of TRP3 channels in Various expression systems. The present study provides a possible explanation for this discrepancy. After overexpression of TRP3 in Chinese hamster ovary cells, whole-cell currents through TRP3 were reversibly inhibited by La3+ with an EC50 of 4 mum. For comparison, the organic blocker SKF96365 required an EC50 of 8 mum. Gd3+ blocked with an EC50 of 0.1 mum, but this block was slow in onset and was not reversible after wash-out. When the two lanthanides were added to the cytosolic side of inside-out patches, block was achieved with considerably lower concentrations (EC50 for La3+, 0.02 mum; EC50 for Gd3+, 0.02 mum). Uptake of La3+ into the cytosol of Chinese hamster ovary cells was demonstrated with intracellular fura a. We conclude that lanthanides block TRP3 more potently from the cytosolic than from the extracellular side of the plasma membrane and that uptake of lanthanides will largely affect the apparent EC50 values after extracellular application.
引用
收藏
页码:37423 / 37428
页数:6
相关论文
共 34 条
  • [1] Submicromolar La3+ concentrations block the calcium release-activated channel, and impair CD69 and CD25 expression in CD3- or thapsigargin-activated Jurkat cells
    Aussel, C
    Marhaba, R
    Pelassy, C
    Breittmayer, JP
    [J]. BIOCHEMICAL JOURNAL, 1996, 313 : 909 - 913
  • [2] Evidence for a role of Trp proteins in the oxidative stress-induced membrane conductances of porcine aortic endothelial cells
    Balzer, M
    Lintschinger, B
    Groschner, K
    [J]. CARDIOVASCULAR RESEARCH, 1999, 42 (02) : 543 - 549
  • [3] On the molecular basis and regulation of cellular capacitative calcium entry: Roles for Trp proteins
    Birnbaumer, L
    Zhu, X
    Jiang, MS
    Boulay, G
    Peyton, M
    Vannier, B
    Brown, D
    Platano, D
    Sadeghi, H
    Stefani, E
    Birnbaumer, M
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) : 15195 - 15202
  • [4] Modulation of Ca2+ entry by polypeptides of the inositol 1,4,5-trisphosphate receptor (IP3R) that bind transient receptor potential (TRP):: Evidence for roles of TRP and IP3R in store depletion-activated Ca2+ entry
    Boulay, G
    Brown, DM
    Qin, N
    Jiang, MS
    Dietrich, A
    Zhu, MX
    Chen, ZG
    Birnbaumer, M
    Mikoshiba, K
    Birnbaumer, L
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (26) : 14955 - 14960
  • [5] Using gadolinium to identify stretch-activated channels: technical considerations
    Caldwell, RA
    Clemo, HF
    Baumgarten, CM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 275 (02): : C619 - C621
  • [6] The transport kinetics of lanthanide species in a single erythrocyte probed by confocal laser scanning microscopy
    Cheng, Y
    Huo, QH
    Lu, JF
    Li, RC
    Wang, K
    [J]. JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 1999, 4 (04): : 447 - 456
  • [7] A heterotrimeric G protein complex couples the muscarinic m1 receptor to phospholipase C-beta
    Dippel, E
    Kalkbrenner, F
    Wittig, B
    Schultz, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) : 1391 - 1396
  • [8] EVANS CH, 1990, BIOCHEMISTRY LANTHAN
  • [9] NONSPECIFIC EFFECTS OF CALCIUM-ENTRY ANTAGONISTS IN MAST-CELLS
    FRANZIUS, D
    HOTH, M
    PENNER, R
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1994, 428 (5-6): : 433 - 438
  • [10] Trp proteins form store-operated cation channels in human vascular endothelial cells
    Groschner, K
    Hingel, S
    Lintschinger, B
    Balzer, M
    Romanin, C
    Zhu, X
    Schreibmayer, W
    [J]. FEBS LETTERS, 1998, 437 (1-2) : 101 - 106