TRPM7 facilitates cholinergic vesicle fusion with the plasma membrane

被引:79
作者
Brauchi, Sebastian
Krapivinsky, Grigory
Krapivinsky, Luba
Clapham, David E.
机构
[1] Childrens Hosp, Howard Hughes Med Inst, Dept Cardiol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurobiol, Boston, MA 02115 USA
关键词
acetylcholine; PC12; pHluorin; transient receptor potential channels; single-vesicle fusion;
D O I
10.1073/pnas.0800881105
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
TRPM7, of the transient receptor potential (TRP) family, is both an ion channel and a kinase. Previously, we showed that TRPM7 is located in the membranes of acetylcholine (ACh)-secreting synaptic vesicles of sympathetic neurons, forms a molecular complex with proteins of the vesicular fusion machinery, and is critical for stimulated neurotransmitter release. Here, we targeted pHluorin to small synaptic-like vesicles (SSLV) in PC12 cells and demonstrate that it can serve as a single-vesicle plasma membrane fusion reporter. In PC12 cells, as in sympathetic neurons, TRPM7 is located in ACh-secreting SSLVs. TRPM7 knockdown by siRNA, or abolishing channel activity by expression of a dominant negative TRPM7 pore mutant, decreased the frequency of spontaneous and voltage-stimulated SSLV fusion events without affecting large dense core vesicle secretion. We conclude that the conductance of TRPM7 across the vesicle membrane is important in SSLV fusion.
引用
收藏
页码:8304 / 8308
页数:5
相关论文
共 54 条
[1]   It's green outside: tracking cell surface proteins with pH-sensitive GFP [J].
Ashby, MC ;
Ibaraki, K ;
Henley, JM .
TRENDS IN NEUROSCIENCES, 2004, 27 (05) :257-261
[2]   Single-vesicle imaging reveals that synaptic vesicle exocytosis and endocytosis are coupled by a single stochastic mode [J].
Balaji, J. ;
Ryan, T. A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (51) :20576-20581
[3]   Quantifying Exocytosis by Combination of Membrane Capacitance Measurements and Total Internal Reflection Fluorescence Microscopy in Chromaffin Cells [J].
Becherer, Ute ;
Pasche, Mathias ;
Nofal, Shahira ;
Hof, Detlef ;
Matti, Ulf ;
Rettig, Jens .
PLOS ONE, 2007, 2 (06)
[4]   OKADAIC ACID DISRUPTS CLUSTERS OF SYNAPTIC VESICLES IN FROG MOTOR-NERVE TERMINALS [J].
BETZ, WJ ;
HENKEL, AW .
JOURNAL OF CELL BIOLOGY, 1994, 124 (05) :843-854
[5]   Rapid vesicular translocation and insertion of TRP channels [J].
Bezzerides, VJ ;
Ramsey, IS ;
Kotecha, S ;
Greka, A ;
Clapham, DE .
NATURE CELL BIOLOGY, 2004, 6 (08) :709-720
[6]   Two forms of single-vesicle astrocyte exocytosis imaged with total internal reflection fluorescence microscopy [J].
Bowser, David N. ;
Khakh, Baljit S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (10) :4212-4217
[7]   In vivo imaging of neuronal activity - Neurotechnique by targeted expression of a genetically encoded probe in the mouse [J].
Bozza, T ;
McGann, JP ;
Mombaerts, P ;
Wachowiak, M .
NEURON, 2004, 42 (01) :9-21
[8]   A monomeric red fluorescent protein [J].
Campbell, RE ;
Tour, O ;
Palmer, AE ;
Steinbach, PA ;
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :7877-7882
[9]   TRP channels as cellular sensors [J].
Clapham, DE .
NATURE, 2003, 426 (6966) :517-524
[10]   TRPM7, a novel regulator of actomyosin contractility and cell adhesion [J].
Clark, K ;
Langeslag, M ;
van Leeuwen, B ;
Ran, L ;
Ryazanov, AG ;
Figdor, CG ;
Moolenaar, WH ;
Jalink, K ;
van Leeuwen, FN .
EMBO JOURNAL, 2006, 25 (02) :290-301