F-Actin and Myosin II Accelerate Catecholamine Release from Chromaffin Granules

被引:83
作者
Berberian, Khajak [1 ,2 ]
Torres, Alexis J. [3 ]
Fang, Qinghua [1 ]
Kisler, Kassandra [1 ]
Lindau, Manfred [1 ]
机构
[1] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Biomed Engn, Ithaca, NY 14853 USA
[3] Cornell Univ, Dept Chem & Biol Chem, Ithaca, NY 14853 USA
基金
美国国家卫生研究院;
关键词
chromaffin cells; exocytosis; actin; myosin II; amperometry; capacitance; fluorescence microscopy; fusion pore; EXOCYTOTIC SECRETION EVENTS; FUSION PORE EXPANSION; LIGHT-CHAIN KINASE; VESICLE FUSION; NEUROENDOCRINE CELLS; MEMBRANE; CYTOSKELETON; DYNAMICS; AMPEROMETRY; TRANSPORT;
D O I
10.1523/JNEUROSCI.2818-08.2009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The roles of nonmuscle myosin II and cortical actin filaments in chromaffin granule exocytosis were studied by confocal fluorescence microscopy, amperometry, and cell-attached capacitance measurements. Fluorescence imaging indicated decreased mobility of granules near the plasma membrane following inhibition of myosin II function with blebbistatin. Slower fusion pore expansion rates and longer fusion pore lifetimes were observed after inhibition of actin polymerization using cytochalasin D. Amperometric recordings revealed increased amperometric spike half-widths without change in quantal size after either myosin II inhibition or actin disruption. These results suggest that actin and myosin II facilitate release from individual chromaffin granules by accelerating dissociation of catecholamines from the intragranular matrix possibly through generation of mechanical forces.
引用
收藏
页码:863 / 870
页数:8
相关论文
共 46 条
[1]   The exocytotic event in chromaffin cells revealed by patch amperometry [J].
Albillos, A ;
Dernick, G ;
Horstmann, H ;
Almers, W ;
deToledo, GA ;
Lindau, M .
NATURE, 1997, 389 (6650) :509-512
[2]  
Amatore C, 1999, CHEM-EUR J, V5, P2151, DOI 10.1002/(SICI)1521-3765(19990702)5:7<2151::AID-CHEM2151>3.0.CO
[3]  
2-R
[4]  
AUNIS D, 1988, J EXP BIOL, V139, P253
[5]   DYNAMICS OF LIGAND-BINDING TO MYOGLOBIN [J].
AUSTIN, RH ;
BEESON, KW ;
EISENSTEIN, L ;
FRAUENFELDER, H ;
GUNSALUS, IC .
BIOCHEMISTRY, 1975, 14 (24) :5355-5373
[6]   DYNAMICS OF CARBON-MONOXIDE BINDING BY HEME PROTEINS [J].
AUSTIN, RH ;
BEESON, K ;
IEISENST.L ;
FRAUENFELDER, H ;
GUNSALUS, IC ;
MARSHALL, VP .
SCIENCE, 1973, 181 (4099) :541-543
[7]   DELAY IN VESICLE FUSION REVEALED BY ELECTROCHEMICAL MONITORING OF SINGLE SECRETORY EVENTS IN ADRENAL CHROMAFFIN CELLS [J].
CHOW, RH ;
VONRUDEN, L ;
NEHER, E .
NATURE, 1992, 356 (6364) :60-63
[8]   Actin in action: the interplay between the actin cytoskeleton and synaptic efficacy [J].
Cingolani, Lorenzo A. ;
Goda, Yukiko .
NATURE REVIEWS NEUROSCIENCE, 2008, 9 (05) :344-356
[9]   Mitochondrial calcium sequestration and protein kinase C cooperate in the regulation of cortical F-actin disassembly and secretion in bovine chromaffin cells [J].
Cuchillo-Ibáñez, I ;
Lejen, T ;
Albillos, A ;
Rosé, SD ;
Olivares, R ;
Villarroya, M ;
García, AG ;
Trifaró, JM .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 560 (01) :63-76
[10]   Resolution of patch capacitance recordings and of fusion pore conductances in small vesicles [J].
Debus, K ;
Lindau, M .
BIOPHYSICAL JOURNAL, 2000, 78 (06) :2983-2997