Measurement of the dynamics of exocytosis and vesicle retrieval at cell populations using a quartz crystal microbalance

被引:63
作者
Cans, AS
Höök, F
Shupliakov, O
Ewing, AG
Eriksson, PS
Brodin, L
Orwar, O [1 ]
机构
[1] Chalmers Univ Technol, Dept Phys Chem, S-41296 Gothenburg, Sweden
[2] Gothenburg Univ, Dept Chem, S-41296 Gothenburg, Sweden
[3] Chalmers Univ Technol, Dept Appl Phys, S-41296 Gothenburg, Sweden
[4] Gothenburg Univ, Dept Appl Phys, S-41296 Gothenburg, Sweden
[5] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
[6] Gothenburg Univ, Sahlgrens Hosp, Inst Clin Neurosci, S-41345 Gothenburg, Sweden
[7] Karolinska Inst, Nobel Inst Neurophysiol, Dept Neurosci, S-10401 Stockholm, Sweden
[8] Chalmers Univ Technol, Microtechnol Ctr, S-41296 Gothenburg, Sweden
关键词
D O I
10.1021/ac010777q
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The quartz crystal microbalance-dissipation technique (QCM-D) is used in two different measurement strategies to monitor the mass change and rigidity of populations of excitable cells during exocytosis and subsequent retrieval of dense-core vesicles. Two cell lines, NG 108-15 and PC 12, were grown to confluence on piezoelectric quartz crystals and were examined separately to demonstrate differences in release and retrieval with cells of different morphology, size, and number of dense-core vesicles. Stimulating the cells to exocytosis with media containing an elevated potassium concentration resulted in an increase in the frequency response corresponding to loss of mass from the cells owing to release of vesicles. In Ca2+-free media, the response was completely abolished. The amplitude and peak area in the frequency response corresponding to mass change with stimulated release was larger for PC 12 cells than for NG 108-15 cells, whereas the initial rate constants for the frequency responses were similar. The data suggest (1) that a greater number and larger size of vesicles in PC 12 cells results in a greater amount of release from these cells vs NG 108-15 cells, (2) the recycling of vesicles utilizes similar fusion/retrieval mechanisms in both cell types, (3) that the control of excess retrieval might be related to the number and size of released vesicles, and (4) that measured retrieval has a rapid onset, masking exocytosis and implying a rapid retrieval mechanism in the early stages of release. These results demonstrate that measurements of complex dynamic processes relating to dense-core vesicle release and retrieval can be simultaneously accomplished using the QCM-D technique.
引用
收藏
页码:5805 / 5811
页数:7
相关论文
共 38 条
[1]   Regulation of dense cove release from neuroendocrine cells revealed by imaging single exocytic events [J].
Angleson, JK ;
Cochilla, AJ ;
Kilic, G ;
Nussinovitch, I ;
Betz, WJ .
NATURE NEUROSCIENCE, 1999, 2 (05) :440-446
[2]   Viscoelastic characterization of electroactive polymer films at the electrode/solution interface [J].
Bandey, HL ;
Hillman, AR ;
Brown, MJ ;
Martin, SJ .
FARADAY DISCUSSIONS, 1997, 107 :105-121
[3]   Modeling the responses of thickness-shear mode resonators under various loading conditions [J].
Bandey, HL ;
Martin, SJ ;
Cernosek, RW ;
Hillman, AR .
ANALYTICAL CHEMISTRY, 1999, 71 (11) :2205-2214
[4]   Imaging exocytosis and endocytosis [J].
Betz, WJ ;
Mao, F ;
Smith, CB .
CURRENT OPINION IN NEUROBIOLOGY, 1996, 6 (03) :365-371
[5]   OPTICAL ANALYSIS OF SYNAPTIC VESICLE RECYCLING AT THE FROG NEUROMUSCULAR-JUNCTION [J].
BETZ, WJ ;
BEWICK, GS .
SCIENCE, 1992, 255 (5041) :200-203
[6]  
Calakos N, 1996, PHYSIOL REV, V76, P1
[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]   Quantitative measurements of released amines from individual exocytosis events [J].
Clark, RA ;
Ewing, AG .
MOLECULAR NEUROBIOLOGY, 1997, 15 (01) :1-16
[9]  
Colliver TL, 2000, J NEUROCHEM, V74, P1086
[10]   VMAT-Mediated changes in quantal size and vesicular volume [J].
Colliver, TL ;
Pyott, SJ ;
Achalabun, M ;
Ewing, AG .
JOURNAL OF NEUROSCIENCE, 2000, 20 (14) :5276-5282