TRPV4 exhibits a functional role in cell-volume regulation

被引:156
作者
Becker, D [1 ]
Blase, C [1 ]
Bereiter-Hahn, J [1 ]
Jendrach, M [1 ]
机构
[1] Univ Frankfurt, Kinemat Cell Res Grp, D-60439 Frankfurt, Germany
关键词
TRPV4; cell-volume regulation; RVD; cytosolic Ca2+ concentration;
D O I
10.1242/jcs.02372
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tight regulation of the cell volume is important for the maintenance of cellular homeostasis. In a hypotonic environment, cells swell owing to osmosis. With many vertebrate cells, swelling is followed by an active reduction of volume, a process called regulatory volume decrease (RVD). A possible participant in RVD is the non-selective cation channel TRPV4, a member of the TRP superfamily that has been shown to react to hypotonic stimuli with a conductance for Ca2+. As a model for cell-volume regulation, we used a human keratinocyte cell line (HaCaT) that produces TRPV4 endogenously. When HaCaT cells were exposed to a hypotonic solution (200 mOsm) maximal swelling was followed by RVD. During swelling and volume regulation, a strong Ca2+ influx was measured. Gd (3+), an inhibitor of TRPV4, blocked RVD of HaCaT cells and the accompanying rise of cytosolic Ca2+. To define the role of TRPV4 in volume regulation, a TRPV4-EGFP fusion protein was produced in CHO cells. CHO cells are unable to undergo RVD under hypotonic conditions and do not produce TRPV4 endogenously. Fluorescence imaging revealed that recombinant TRPV4 was localized to the cell membrane. Production of TRPV4 enabled CHO cells to undergo typical RVD after hypo-osmolarity-induced cell swelling. RVD of TRPV4-transfected CHO cells was significantly reduced by Gd3+ treatment or in Ca2+-free solution. Taken together, these results show a direct participation of TRPV4 in RVD.
引用
收藏
页码:2435 / 2440
页数:6
相关论文
共 28 条
  • [1] Transient receptor potential vanilloid 4 is essential in chemotherapy-induced neuropathic pain in the rat
    Alessandri-Haber, N
    Dina, OA
    Yeh, JJ
    Parada, CA
    Reichling, DB
    Levine, JD
    [J]. JOURNAL OF NEUROSCIENCE, 2004, 24 (18) : 4444 - 4452
  • [2] Swelling-activated Ca2+ entry via TRPV4 channel is defective in cystic fibrosis airway epithelia
    Arniges, M
    Vázquez, E
    Fernández-Fernández, JM
    Valverde, MA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (52) : 54062 - 54068
  • [3] Isolation of proximal and distal tubule cells from human kidney by immunomagnetic separation
    Baer, PC
    Nockher, WA
    Haase, W
    Scherberich, JE
    [J]. KIDNEY INTERNATIONAL, 1997, 52 (05) : 1321 - 1331
  • [4] NORMAL KERATINIZATION IN A SPONTANEOUSLY IMMORTALIZED ANEUPLOID HUMAN KERATINOCYTE CELL-LINE
    BOUKAMP, P
    PETRUSSEVSKA, RT
    BREITKREUTZ, D
    HORNUNG, J
    MARKHAM, A
    FUSENIG, NE
    [J]. JOURNAL OF CELL BIOLOGY, 1988, 106 (03) : 761 - 771
  • [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] Maxi K+ channel mediates regulatory volume decrease response in a human bronchial epithelial cell line
    Fernández-Fernández, JM
    Nobles, M
    Currid, A
    Vázquez, E
    Valverde, MA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 283 (06): : C1705 - C1714
  • [7] Güler AD, 2002, J NEUROSCI, V22, P6408
  • [8] JENDRACH M, 2004, EUR J CELL BIOL S, V83, P54
  • [9] Vanilloid receptor-related osmotically activated channel (VR-OAC), a candidate vertebrate osmoreceptor
    Liedtke, W
    Choe, Y
    Martí-Renom, MA
    Bell, AM
    Denis, CS
    Sali, A
    Hudspeth, AJ
    Friedman, JM
    Heller, S
    [J]. CELL, 2000, 103 (03) : 525 - 535
  • [10] Mammalian TRPV4 (VR-OAC) directs behavioral responses to osmotic and mechanical stimuli in Caenorhabditis elegans
    Liedtke, W
    Tobin, DM
    Bargmann, CI
    Friedman, JM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 : 14531 - 14536