HUMAN NEUTROPHIL MOTILITY - TIME-DEPENDENT 3-DIMENSIONAL SHAPE AND GRANULE DIFFUSION

被引:29
作者
FELDER, S [1 ]
KAM, Z [1 ]
机构
[1] WEIZMANN INST SCI, DEPT CHEM IMMUNOL, IL-76100 REHOVOT, ISRAEL
来源
CELL MOTILITY AND THE CYTOSKELETON | 1994年 / 28卷 / 04期
关键词
PMN; 3-D VIDEO-MICROSCOPY; QUASI-ELASTIC LASER LIGHT SCATTERING; CHEMOTAXIS;
D O I
10.1002/cm.970280403
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The locomotion of human polymorphonuclear leukocytes (PMNs) was studied with two complementary methods: Three-dimensional shapes were reconstructed from time series of optical sectioning microscopy using differential interference contrast (DIC) optics, and the diffusion of cytoplasm granules within individual cells was measured using quasielastic laser light scattering (QELS). The three-dimensional cell edges outlined in the optical sections were analyzed qualitatively in time-lapse film strips and quantitatively from morphometry. The fastest locomotion occurred in chemotactic gradient with cell velocity that oscillated between 10 and 30 mu m/min with a period of 50-55 seconds. Within the periodic bursts of speed, a fibroblast-like locomotory cycle was observed, with leading lamella extended and contacts formed with the substrate surface, followed by rapid motion of the cell body and nucleus over the immobile contacts. Consistent with this apparent staged motion, correlation analysis revealed a phase lag of 2-3 seconds in velocities between the bottom (ventral) and the top layers of the cell. In addition there was a tendency to a lower cell profile at times of higher velocity. The diffusion of natural cytoplasmic granules within resting PMNs was not affected by cytoskeleton disrupting drugs. During the stage of most rapid motion, when cytoplasmic streaming could be seen, diffusion of the granules decreased two- to 2.5-fold, and then returned to resting levels. These observations suggest that PMN locomotion consists of extensions near the surface to form forward contacts and then stiffening or possibly contraction of the cytoskeleton when the body of the cell is moved forward. Three-dimensional movies of PMN cells are included in the video supplement. (C) 1994 Wiley-Liss, Inc.
引用
收藏
页码:285 / 302
页数:18
相关论文
共 46 条
[1]   LOCOMOTION OF FIBROBLASTS IN CULTURE .2. RUFFLING [J].
ABERCROMBIE, M ;
HEAYSMAN, JE ;
PEGRUM, SM .
EXPERIMENTAL CELL RESEARCH, 1970, 60 (03) :437-+
[2]   LOCOMOTION OF FIBROBLASTS IN CULTURE .1. MOVEMENTS OF LEADING EDGE [J].
ABERCROMBIE, M ;
HEAYSMAN, JE ;
PEGRUM, SM .
EXPERIMENTAL CELL RESEARCH, 1970, 59 (03) :393-+
[3]   LOCOMOTION OF FIBROBLASTS IN CULTURE .5. SURFACE MARKING WITH CONCANAVALIN A [J].
ABERCROMBIE, M ;
HEAYSMAN, JE ;
PEGRUM, SM .
EXPERIMENTAL CELL RESEARCH, 1972, 73 (02) :536-+
[4]  
AGARD DA, 1984, ANNU REV BIOPHYS BIO, V13, P191
[5]   3-DIMENSIONAL ARCHITECTURE OF A POLYTENE NUCLEUS [J].
AGARD, DA ;
SEDAT, JW .
NATURE, 1983, 302 (5910) :676-681
[6]   CHARACTERIZATION OF INTERNALIZATION AND ENDOSOME FORMATION OF EPIDERMAL GROWTH-FACTOR IN TRANSFECTED NIH-3T3 CELLS BY COMPUTERIZED IMAGE-INTENSIFIED 3-DIMENSIONAL FLUORESCENCE MICROSCOPY [J].
BENVENISTE, M ;
SCHLESSINGER, J ;
KAM, Z .
JOURNAL OF CELL BIOLOGY, 1989, 109 (05) :2105-2115
[7]  
Berne B. J., 1976, DOVER BOOKS PHYS SER
[8]  
Bershadsky AD., 1988, CYTOSKELETON, V1st
[9]  
Bloom W., 1975, TXB HISTOLOGY
[10]   CORTICAL FLOW IN ANIMAL-CELLS [J].
BRAY, D ;
WHITE, JG .
SCIENCE, 1988, 239 (4842) :883-888