Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels

被引:2153
作者
Coste, Bertrand [1 ]
Mathur, Jayanti [2 ]
Schmidt, Manuela [1 ]
Earley, Taryn J. [1 ]
Ranade, Sanjeev [1 ]
Petrus, Matt J. [2 ]
Dubin, Adrienne E. [1 ]
Patapoutian, Ardem [1 ,2 ]
机构
[1] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
[2] Novartis Res Fdn GNF, Genom Inst, San Diego, CA 92121 USA
关键词
CURRENTS; NEURONS; PROTEIN; TRANSDUCTION;
D O I
10.1126/science.1193270
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Mechanical stimuli drive many physiological processes, including touch and pain sensation, hearing, and blood pressure regulation. Mechanically activated (MA) cation channel activities have been recorded in many cells, but the responsible molecules have not been identified. We characterized a rapidly adapting MA current in a mouse neuroblastoma cell line. Expression profiling and RNA interference knockdown of candidate genes identified Piezo1 (Fam38A) to be required for MA currents in these cells. Piezo1 and related Piezo2 (Fam38B) are vertebrate multipass transmembrane proteins with homologs in invertebrates, plants, and protozoa. Overexpression of mouse Piezo1 or Piezo2 induced two kinetically distinct MA currents. Piezos are expressed in several tissues, and knockdown of Piezo2 in dorsal root ganglia neurons specifically reduced rapidly adapting MA currents. We propose that Piezos are components of MA cation channels.
引用
收藏
页码:55 / 60
页数:6
相关论文
共 35 条
  • [1] Noxious cold ion channel TRPA1 is activated by pungent compounds and bradykinin
    Bandell, M
    Story, GM
    Hwang, SW
    Viswanath, V
    Eid, SR
    Petrus, MJ
    Earley, TJ
    Patapoutian, A
    [J]. NEURON, 2004, 41 (06) : 849 - 857
  • [2] Cellular and Molecular Mechanisms of Pain
    Basbaum, Allan I.
    Bautista, Diana M.
    Scherrer, Gregory
    Julius, David
    [J]. CELL, 2009, 139 (02) : 267 - 284
  • [3] High-speed pressure clamp
    Besch, SR
    Suchyna, T
    Sachs, F
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2002, 445 (01): : 161 - 166
  • [4] Purinergic mechanosensory transduction and visceral pain
    Burnstock, Geoffrey
    [J]. MOLECULAR PAIN, 2009, 5
  • [5] Neurosensory mechanotransduction
    Chalfie, Martin
    [J]. NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (01) : 44 - 52
  • [6] A novel mechanosensitive channel identified in sensory neurons
    Cho, Hawon
    Koo, Jae Yeon
    Kim, Sangsung
    Park, Sung Pyo
    Yang, Youngduk
    Oh, Uhtaek
    [J]. EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (10) : 2543 - 2550
  • [7] RESPONSE LATENCY OF VERTEBRATE HAIR-CELLS
    COREY, DP
    HUDSPETH, AJ
    [J]. BIOPHYSICAL JOURNAL, 1979, 26 (03) : 499 - 506
  • [8] Pharmacological dissection and distribution of NaN/Nav1.9, T-type Ca2+ currents, and mechanically activated cation currents in different populations of DRG neurons
    Coste, Bertrand
    Crest, Marcel
    Delmas, Patrick
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2007, 129 (01) : 57 - 77
  • [9] High-Threshold Mechanosensitive Ion Channels Blocked by a Novel Conopeptide Mediate Pressure-Evoked Pain
    Drew, Liam J.
    Rugiero, Francois
    Cesare, Paolo
    Gale, Jonathan E.
    Abrahamsen, Bjarke
    Bowden, Sarah
    Heinzmann, Sebastian
    Robinson, Michelle
    Brust, Andreas
    Colless, Barbara
    Lewis, Richard J.
    Wood, John N.
    [J]. PLOS ONE, 2007, 2 (06):
  • [10] Acid-sensing ion channels ASIC2 and ASIC3 do not contribute to mechanically activated currents in mammalian sensory neurones
    Drew, LJ
    Rohrer, DK
    Price, MP
    Blaver, KE
    Cockayne, DA
    Cesare, P
    Wood, JN
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2004, 556 (03): : 691 - 710