Quantifying axial secretory-granule motion with variable-angle evanescent-field excitation

被引:30
作者
Loerke, D
Stühmer, W
Oheim, M
机构
[1] Ecole Super Phys & Chim Ind Ville Paris, F-75005 Paris, France
[2] Max Planck Inst Expt Med, Dept Mol Biol & Neuronal Signals, D-37075 Gottingen, Germany
关键词
3-D reconstruction; optical sectioning; secretion exocytosis; fluorescence; evanescent-wave microscopy; total internal reflection;
D O I
10.1016/S0165-0270(02)00178-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The trajectory of secretory vesicles to their fusion sites at the plasma membrane is expected to give insight into the mechanisms that underlie vesicle transport, maturation and the initiation of membrane fusion. Evanescent-wave (EW) microscopy allows the tracking of fluorescently labeled granules and vesicles prior to fusion with nanometer precision in xy-direction. At the same time, the exponential sensitivity of granular fluorescence to experimental parameters can preclude quantitative estimates of the granule's approach to the plasma membrane. Thus, it has remained controversial to which extent axial distance can be obtained from simple intensity measurements. We used the information contained in a stack of images acquired at 80-125 nm penetration depth of the EW field to estimate individual granule diameter and axial distance. A population analysis on 90 granules revealed an average diameter of 305 +/- 47 nm, below the diffraction-limited 3 52 +/- 31 nm obtained from xy measurements at fixed depth penetration. Stimulation of exocytosis by potassium depolarization resulted in the selective loss of the 18 +/- 5% of granules located closest to the plasma membrane, while a second population of granules located 60 nm deeper within the cytoplasm increased by recruitment of granules previously located at greater than or equal to120 nm depth. These measurements extend and corroborate previous observations at fixed penetration depth of functionally distinct granule populations. Parameters influencing the accuracy of the parameter estimation are evaluated in the appendix. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:65 / 73
页数:9
相关论文
共 32 条
[1]  
Axelrod D, 1991, TOPICS FLUORESCENCE, V3, P289
[2]  
BRYNGDAHL O, 1973, PROGR OPTICS, V11, P169
[3]  
Bundy A, 2002, BIOPHYS J, V82, p615A
[4]   QUANTITATIVE-ANALYSIS OF VARIABLE-ANGLE TOTAL INTERNAL-REFLECTION FLUORESCENCE MICROSCOPY (VA-TIRFM) OF CELL SUBSTRATE CONTACTS [J].
BURMEISTER, JS ;
TRUSKEY, GA ;
REICHERT, WM .
JOURNAL OF MICROSCOPY-OXFORD, 1994, 173 :39-51
[5]   Variable-angle time-resolved evanescent wave-induced fluorescence spectroscopy (VATR-EWIFS): A technique for concentration profiling fluorophores at dielectric interfaces [J].
Byrne, CD ;
de Mello, AJ ;
Barnes, WL .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (50) :10326-10333
[6]   AUTOMATED DETECTION AND TRACKING OF INDIVIDUAL AND CLUSTERED CELL-SURFACE LOW-DENSITY-LIPOPROTEIN RECEPTOR MOLECULES [J].
GHOSH, RN ;
WEBB, WW .
BIOPHYSICAL JOURNAL, 1994, 66 (05) :1301-1318
[7]   Restriction of secretory granule motion near the plasma membrane of chromaffin cells [J].
Johns, LM ;
Levitan, ES ;
Shelden, EA ;
Holz, RW ;
Axelrod, D .
JOURNAL OF CELL BIOLOGY, 2001, 153 (01) :177-190
[8]   MAPPING WHISPERING-GALLERY MODES IN MICROSPHERES WITH A NEAR-FIELD PROBE [J].
KNIGHT, JC ;
DNBREUIL, N ;
SANDOGHDAR, V ;
HARE, J ;
LEFEVRESEGUIN, V ;
RAIMOND, JM ;
HAROCHE, S .
OPTICS LETTERS, 1995, 20 (14) :1515-1517
[9]   Ca2+-triggered peptide secretion neurotechnique in single cells imaged with green fluorescent protein and evanescent-wave microscopy [J].
Lang, T ;
Wacker, I ;
Steyer, J ;
Kaether, C ;
Wunderlich, I ;
Soldati, T ;
Gerdes, HH ;
Almers, W .
NEURON, 1997, 18 (06) :857-863
[10]   STRUCTURAL ORGANIZATION OF INTERPHASE 3T3-FIBROBLASTS STUDIED BY TOTAL INTERNAL-REFLECTION FLUORESCENCE MICROSCOPY [J].
LANNI, F ;
WAGGONER, AS ;
TAYLOR, DL .
JOURNAL OF CELL BIOLOGY, 1985, 100 (04) :1091-1102