Functional roles of TRPC channels in the developing brain

被引:52
作者
Tai, Yilin [2 ]
Feng, Shengjie [2 ]
Du, Wanlu [2 ]
Wang, Yizheng [1 ]
机构
[1] Shanghai Inst Biol Sci, Inst Neurosci, Lab Neural Signal Transduct, Shanghai 200031, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Shanghai 200031, Peoples R China
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2009年 / 458卷 / 02期
基金
中国国家自然科学基金;
关键词
Neurone; Brain; Development; TRP channels; Synaptic mechanisms; INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS; CEREBELLAR GRANULE NEURONS; NERVE GROWTH CONES; NEUROTROPHIC FACTOR; CA2+ ENTRY; CALCIUM TRANSIENTS; CELL-PROLIFERATION; DENDRITIC GROWTH; ACTIVATION; PROTEIN;
D O I
10.1007/s00424-008-0618-y
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Transient receptor potential canonical (TRPC) channels are Ca2+-permeable, nonselective cation channels formed by homomeric or heteromeric complexes of TRPC proteins that contain six transmembrane domains. These channels can be activated through a phospholipase-C-dependent mechanism, making them sensors for environmental cues. Their expression begins early in embryonic days and remains in adulthood. These channels have important roles in the processes of neuronal development, including neural stem cell proliferation, cerebellar granule cell survival, axon path finding, neuronal morphogenesis, and synaptogenesis. In this review, we will discuss functional implications of TRPC channels during brain development.
引用
收藏
页码:283 / 289
页数:7
相关论文
共 77 条
[11]   Cytoskeletal dynamics and transport in growth cone motility and axon guidance [J].
Dent, EW ;
Gertler, FB .
NEURON, 2003, 40 (02) :209-227
[12]   Increased vascular smooth muscle contractility in TRPC6-/- mice [J].
Dietrich, A ;
Schnitzler, MMY ;
Gollasch, M ;
Gross, V ;
Storch, U ;
Dubrovska, G ;
Obst, M ;
Yildirim, E ;
Salanova, B ;
Kalwa, H ;
Essin, K ;
Pinkenburg, O ;
Luft, FC ;
Gudermann, T ;
Birnbaumer, L .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (16) :6980-6989
[13]   Pressure-induced and store-operated cation influx in vascular smooth muscle cells is independent of TRPC1 [J].
Dietrich, Alexander ;
Kalwa, Hermann ;
Storch, Ursula ;
Mederos y Schnitzler, Michael ;
Salanova, Birgit ;
Pinkenburg, Olaf ;
Dubrovska, Galyna ;
Essin, Kirill ;
Gollasch, Maik ;
Birnbaumer, Lutz ;
Gudermann, Thomas .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2007, 455 (03) :465-477
[14]   Signaling to the nucleus by an L-type calcium channel - Calmodulin complex through the MAP kinase pathway [J].
Dolmetsch, RE ;
Pajvani, U ;
Fife, K ;
Spotts, JM ;
Greenberg, ME .
SCIENCE, 2001, 294 (5541) :333-339
[15]   Lack of an endothelial store-operated Ca2+ current impairs agonist-dependent vasorelaxation in TRP4-/- mice [J].
Freichel, M ;
Suh, SH ;
Pfeifer, A ;
Schweig, U ;
Trost, C ;
Weissgerber, P ;
Biel, M ;
Philipp, S ;
Freise, D ;
Droogmans, G ;
Hofmann, F ;
Flockerzi, V ;
Nilius, B .
NATURE CELL BIOLOGY, 2001, 3 (02) :121-127
[16]   REQUIREMENT FOR BDNF IN ACTIVITY-DEPENDENT SURVIVAL OF CORTICAL-NEURONS [J].
GHOSH, A ;
CARNAHAN, J ;
GREENBERG, ME .
SCIENCE, 1994, 263 (5153) :1618-1623
[17]   Selective association of TRPC channel subunits in rat brain synaptosomes [J].
Goel, M ;
Sinkins, WG ;
Schilling, WP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (50) :48303-48310
[18]   Filopodial calcium transients promote substrate-dependent growth cone turning [J].
Gomez, TM ;
Robles, E ;
Poo, MM ;
Spitzer, NC .
SCIENCE, 2001, 291 (5510) :1983-1987
[19]   TRPC5 is a regulator of hippocampal neurite length and growth cone morphology [J].
Greka, A ;
Navarro, B ;
Oancea, E ;
Duggan, A ;
Clapham, DE .
NATURE NEUROSCIENCE, 2003, 6 (08) :837-845
[20]   DISTINCT ASPECTS OF NEURONAL DIFFERENTIATION ENCODED BY FREQUENCY OF SPONTANEOUS CA2+ TRANSIENTS [J].
GU, XN ;
SPITZER, NC .
NATURE, 1995, 375 (6534) :784-787