INTRACELLULAR CALCIUM LEVELS CORRELATE WITH SPEED AND PERSISTENT FORWARD MOTION IN MIGRATING NEUTROPHILS

被引:68
作者
MANDEVILLE, JTH
GHOSH, RN
MAXFIELD, FR
机构
[1] COLUMBIA UNIV, COLL PHYS & SURG, DEPT PATHOL, NEW YORK, NY 10032 USA
[2] COLUMBIA UNIV, COLL PHYS & SURG, DEPT PHYSIOL, NEW YORK, NY 10032 USA
关键词
D O I
10.1016/S0006-3495(95)80336-X
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The relationship between cytosolic free calcium concentration ([Ca2+](i)) and human neutrophil motility was studied by video microscopy. Neutrophils stimulated by a uniform concentration of an N-formylated peptide chemoattractant (f-Met-Leu-Phe) were tracked during chemokinetic migration on albumin, fibronectin, and vitronectin. [Ca2+](i) buffering with quin2 resulted in significant decreases in mean speed on albumin. To further characterize the relationship between [Ca2+](i) changes and motility we carried out a cross-correlation analysis of [Ca2+](i) with several motility parameters. Cross-correlations between [Ca2+](i) and each cell's speed, angle changes, turn strength, and persistent forward motion revealed (i) a positive correlation between [Ca2+](i) and cell speed (p < 0.05), (ii) no significant correlation between turns and calcium spikes, and (iii) the occurrence of turns during periods of low speed. Significant negative correlations between [Ca2+](i) and angle change were noted on the high adhesion substrates vitronectin and fibronectin but not on the low adhesion substrate albumin. These data imply that there is a general temporal relationship between [Ca2+](i), speed, and persistent motion. However, the correlations are not sufficiently strong to imply that changes in [Ca2-](i) are required proximal signals for velocity changes.
引用
收藏
页码:1207 / 1217
页数:11
相关论文
共 51 条
[11]  
DUNN GA, 1993, BLOOD CELLS, V19, P25
[12]  
DUNN GA, 1987, J CELL SCI, P81
[13]  
ELIOTT S, 1993, J CELL SCI, V104, P457
[14]   SIMULTANEOUS NOMARSKI AND FLUORESCENCE IMAGING DURING VIDEO MICROSCOPY OF CELLS [J].
FOSKETT, JK .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (04) :C566-C571
[15]   MYOSIN-I IS LOCATED AT THE LEADING EDGES OF LOCOMOTING DICTYOSTELIUM AMEBAS [J].
FUKUI, Y ;
LYNCH, TJ ;
BRZESKA, H ;
KORN, ED .
NATURE, 1989, 341 (6240) :328-331
[16]   FLUORESCENT ACTIN ANALOGS WITH A HIGH-AFFINITY FOR PROFILIN IN-VITRO EXHIBIT AN ENHANCED GRADIENT OF ASSEMBLY IN LIVING CELLS [J].
GIULIANO, KA ;
TAYLOR, DL .
JOURNAL OF CELL BIOLOGY, 1994, 124 (06) :971-983
[17]  
GLANTZ SA, 1992, PRIMER BIOSTATISTICS
[18]  
GOLLNICK F, 1991, EUR J CELL BIOL, V55, P262
[19]   FLUORESCENCE ANISOTROPY IMAGING MICROSCOPY MAPS CALMODULIN-BINDING DURING CELLULAR CONTRACTION AND LOCOMOTION [J].
GOUGH, AH ;
TAYLOR, DL .
JOURNAL OF CELL BIOLOGY, 1993, 121 (05) :1095-1107
[20]  
GRULER H, 1984, BLOOD CELLS, V10, P61