Cell volume measurement using scanning ion conductance microscopy

被引:129
作者
Korchev, YE
Gorelik, J
Lab, MJ
Sviderskaya, EV
Johnston, CL
Coombes, CR
Vodyanoy, I
Edwards, CRW
机构
[1] Imperial Coll Sch Med, MRC, Ctr Clin Sci, Div Med, London W12 0NN, England
[2] Imperial Coll Sch Med, Div Natl Heart & Lung Inst, London W6 8RP, England
[3] Univ London St Georges Hosp, Sch Med, Dept Anat & Dev Biol, London SW17 0RE, England
[4] Off Naval Res Int Field Off, London NW1 5TH, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0006-3495(00)76607-0
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
We report a novel scanning ion conductance microscopy (SICM) technique for assessing the volume of living cells, which allows quantitative, high-resolution characterization of dynamic changes in cell volume while retaining the cell functionality. The technique can measure a wide range of volumes from 10(-19) to 10(-9) liter, The cell volume, as well as the volume of small cellular structures such as lamelopodia, dendrites, processes, or microvilli, can be measured with the 2.5 x 10(-20) liter resolution. The sample does not require any preliminary preparation before cell volume measurement. Both cell volume and surface characteristics can be simultaneously and continuously assessed during relatively long experiments. The SICM method can also be used for rapid estimation of the changes in cell volume. These are important when monitoring the cell responses to different physiological stimuli.
引用
收藏
页码:451 / 457
页数:7
相关论文
共 32 条
[1]   CELL-VOLUME CHANGES UPON SODIUM-PUMP INHIBITION IN HELIX-ASPERSA NEURONS [J].
ALVAREZLEEFMANS, FJ ;
GAMINO, SM ;
REUSS, L .
JOURNAL OF PHYSIOLOGY-LONDON, 1992, 458 :603-619
[2]   TRANSMEMBRANE ION MOVEMENTS ELICITED BY SODIUM-PUMP INHIBITION IN HELIX-ASPERSA NEURONS [J].
ALVAREZLEEFMANS, FJ ;
CRUZBLANCA, H ;
GAMINO, SM ;
ALTAMIRANO, J ;
NANI, A ;
REUSS, L .
JOURNAL OF NEUROPHYSIOLOGY, 1994, 71 (05) :1787-1796
[3]   PROTEIN IMAGES OBTAINED BY STM, AFM AND TEM [J].
ARAKAWA, H ;
UMEMURA, K ;
IKAI, A .
NATURE, 1992, 358 (6382) :171-&
[4]   CHEMICAL IMAGING OF SURFACES WITH THE SCANNING ELECTROCHEMICAL MICROSCOPE [J].
BARD, AJ ;
FAN, FRF ;
PIERCE, DT ;
UNWIN, PR ;
WIPF, DO ;
ZHOU, FM .
SCIENCE, 1991, 254 (5028) :68-74
[5]   THE FGF FAMILY OF GROWTH-FACTORS AND ONCOGENES [J].
BASILICO, C ;
MOSCATELLI, D .
ADVANCES IN CANCER RESEARCH, 1992, 59 :115-165
[6]   ATOMIC FORCE MICROSCOPE [J].
BINNIG, G ;
QUATE, CF ;
GERBER, C .
PHYSICAL REVIEW LETTERS, 1986, 56 (09) :930-933
[7]  
BINNIG G, 1982, HELV PHYS ACTA, V55, P726
[8]   VOLUME CHANGES IN SINGLE N1E-115 NEUROBLASTOMA-CELLS MEASURED WITH A FLUORESCENT-PROBE [J].
CROWE, WE ;
ALTAMIRANO, J ;
HUERTO, L ;
ALVAREZLEEFMANS, FJ .
NEUROSCIENCE, 1995, 69 (01) :283-296
[9]   Four-dimensional imaging of living chondrocytes in cartilage using confocal microscopy: A pragmatic approach [J].
Errington, RJ ;
Fricker, MD ;
Wood, JL ;
Hall, AC ;
White, NS .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1997, 272 (03) :C1040-C1051
[10]   Plasma membrane water permeability of cultured cells and epithelia measured by light microscopy with spatial filtering [J].
Farinas, J ;
Kneen, M ;
Moore, M ;
Verkman, AS .
JOURNAL OF GENERAL PHYSIOLOGY, 1997, 110 (03) :283-296