Forcing open TRP channels: Mechanical gating as a unifying activation mechanism

被引:119
作者
Liu, Chao [1 ,2 ]
Montell, Craig [1 ,2 ]
机构
[1] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
关键词
TRP channel; Mechanical gating; Mechanosensitive channels; PLC-dependent signaling; INTEGRAL MEMBRANE-PROTEIN; ION-CHANNEL; DROSOPHILA PHOTORECEPTORS; MECHANOTRANSDUCTION CHANNEL; TRANSDUCTION CHANNEL; CAPSAICIN RECEPTOR; TOUCH SENSATION; ANKYRIN REPEATS; CELLS; COLD;
D O I
10.1016/j.bbrc.2015.02.067
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
Transient receptor potential (TRP) proteins are cation channels that comprise a superfamily of molecular sensors that enable animals to detect a wide variety of environmental stimuli. This versatility enables vertebrate and invertebrate TRP channels to function in a diversity of senses, ranging from vision to taste, smell, touch, hearing, proprioception and thermosensation. Moreover, many individual TRP channels are activated through a surprising range of sensory stimuli. The multitasking nature of TRP channels raises the question as to whether seemingly disparate activators gate TRPs through common strategies. In this regard, a recent major advance is the discovery that a phospholipase C (PLC)-dependent signaling cascade activates the TRP channels in Drosophila photoreceptor cells through generation of force in the lipid-bilayer. The premise of this review is that mechanical force is a unifying, common strategy for gating TRP channels. In addition to several TRP channels that function in mechanosensation and are gated by force applied to the cells, changes in temperature or alterations in the concentration of lipophilic second messengers through stimulation of signaling cascades, cause architectural modifications of the cell membrane, which in turn activate TRP channels through mechanical force. Consequently, TRPs are capable of functioning as stretch-activated channels, even in cases in which the stimuli that initiate the signaling cascades are not mechanical. We propose that most TRPs are actually mechanosensitive channels (MSCs), which undergo conformational changes in response to tension imposed on the lipid bilayer, resulting in channel gating. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:22 / 25
页数:4
相关论文
共 59 条
[1]   ISOLATION OF A PUTATIVE PHOSPHOLIPASE-C GENE OF DROSOPHILA, NORPA, AND ITS ROLE IN PHOTOTRANSDUCTION [J].
BLOOMQUIST, BT ;
SHORTRIDGE, RD ;
SCHNEUWLY, S ;
PERDEW, M ;
MONTELL, C ;
STELLER, H ;
RUBIN, G ;
PAK, WL .
CELL, 1988, 54 (05) :723-733
[2]   TRPV1 structures in distinct conformations reveal activation mechanisms [J].
Cao, Erhu ;
Liao, Maofu ;
Cheng, Yifan ;
Julius, David .
NATURE, 2013, 504 (7478) :113-+
[3]   TRPV1 Channels Are Intrinsically Heat Sensitive and Negatively Regulated by Phosphoinositide Lipids [J].
Cao, Erhu ;
Cordero-Morales, Julio F. ;
Liu, Beiying ;
Qin, Feng ;
Julius, David .
NEURON, 2013, 77 (04) :667-679
[4]   The capsaicin receptor: a heat-activated ion channel in the pain pathway [J].
Caterina, MJ ;
Schumacher, MA ;
Tominaga, M ;
Rosen, TA ;
Levine, JD ;
Julius, D .
NATURE, 1997, 389 (6653) :816-824
[5]   ODORANT-SPECIFIC ADAPTATION PATHWAYS GENERATE OLFACTORY PLASTICITY IN C-ELEGANS [J].
COLBERT, HA ;
BARGMANN, CI .
NEURON, 1995, 14 (04) :803-812
[6]  
Consortium T.I.P.K.D., 1995, CELL, V81, P289
[7]   Transient Receptor Potential Channels and Mechanosensation [J].
Eijkelkamp, Niels ;
Quick, Kathryn ;
Wood, John N. .
ANNUAL REVIEW OF NEUROSCIENCE, VOL 36, 2013, 36 :519-546
[8]   The Capsaicin Receptor TRPV1 Is a Crucial Mediator of the Noxious Effects of Mustard Oil [J].
Everaerts, Wouter ;
Gees, Maarten ;
Alpizar, Yeranddy A. ;
Farre, Ricard ;
Leten, Cindy ;
Apetrei, Aurelia ;
Dewachter, Ilse ;
van Leuven, Fred ;
Vennekens, Rudi ;
De Ridder, Dirk ;
Nilius, Bernd ;
Voets, Thomas ;
Talavera, Karel .
CURRENT BIOLOGY, 2011, 21 (04) :316-321
[9]   TRP Channels [J].
Gees, Maarten ;
Owsianik, Grzegorz ;
Nilius, Bernd ;
Voets, Thomas .
COMPREHENSIVE PHYSIOLOGY, 2012, 2 (01) :563-608
[10]  
HARDIE RC, 1991, J NEUROSCI, V11, P3079