Secondary ion MS imaging to relatively quantify cholesterol in the membranes of individual cells from differentially treated populations

被引:83
作者
Ostrowski, Sara G. [1 ]
Kurczy, Michael E. [1 ]
Roddy, Thomas P. [1 ]
Winograd, Nicholas [1 ]
Ewing, Andrew G. [1 ]
机构
[1] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
关键词
D O I
10.1021/ac061825f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Time-of-flight secondary ion mass spectrometry (TOF-SIMS) is a well-established bioanalytical method for directly imaging the chemical distribution across single cells. Here we report a protocol for the use of SIMS imaging to comparatively quantify the relative difference in cholesterol level between the plasma membranes of two cells. It should be possible to apply this procedure to the study of other selected lipids. This development enables direct comparison of the chemical effects of different drug treatments and incubation conditions in the plasma membrane at the single-cell level. Relative, quantitative TOF-SIMS imaging has been used here to compare macrophage cells treated to contain elevated levels of cholesterol with respect to control cells. In situ fluorescence microscopy with two different membrane dyes was used to discriminate morphologically similar but differentially treated cells prior to SIMS analysis. SIMS images of fluorescently identified cells reveal that the two populations of cells have distinct outer leaflet membrane compositions with the membranes of the cholesterol-treated macrophages containing more than twice the amount of cholesterol of control macrophages. Relative quantification with SIMS to compare the chemical composition of single cells can provide valuable information about normal biological functions, causative agents of diseases, and possible therapies for diseases.
引用
收藏
页码:3554 / 3560
页数:7
相关论文
共 43 条
[1]   Gold-enhanced biomolecular surface imaging of cells and tissue by SIMS and MALDI mass spectrometry [J].
Altelaar, AFM ;
Klinkert, I ;
Jalink, K ;
de Lange, RPJ ;
Adan, RAH ;
Heeren, RMA ;
Piersma, SR .
ANALYTICAL CHEMISTRY, 2006, 78 (03) :734-742
[2]  
Benninghoven A., 1987, Secondary Ion Mass Spectrometry: Basic Concepts, Instrumental Aspects, Applications and Trends
[3]   Measurements of catecholamine-mediated apoptosis of immunocompetent cells by capillary electrophoresis [J].
Bergquist, J ;
Josefsson, E ;
Tarkowski, A ;
Ekman, R ;
Ewing, A .
ELECTROPHORESIS, 1997, 18 (10) :1760-1766
[4]   Molecule specific imaging of freeze-fractured, frozen-hydrated model membrane systems using mass spectrometry [J].
Cannon, DM ;
Pacholski, ML ;
Winograd, N ;
Ewing, AG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (04) :603-610
[5]   Quantitative chemical analysis of single cells [J].
Cannon, DM ;
Winograd, N ;
Ewing, AG .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2000, 29 :239-263
[6]   Subcellular imaging by dynamic SIMS ion microscopy [J].
Chandra, S ;
Smith, DR ;
Morrison, GH .
ANALYTICAL CHEMISTRY, 2000, 72 (03) :104A-114A
[7]   SAMPLE PREPARATION OF ANIMAL-TISSUES AND CELL-CULTURES FOR SECONDARY ION MASS-SPECTROMETRY (SIMS) MICROSCOPY [J].
CHANDRA, S ;
MORRISON, GH .
BIOLOGY OF THE CELL, 1992, 74 (01) :31-42
[8]   Probing cell chemistry with time-of-flight secondary ion mass spectrometry: development and exploitation of instrumentation for studies of frozen-hydrated biological material [J].
Cliff, B ;
Lockyer, N ;
Jungnickel, H ;
Stephens, G ;
Vickerman, JC .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2003, 17 (19) :2163-2167
[9]   Atomic and molecular imaging at the single-cell level with TOF-SIMS [J].
Colliver, TL ;
Brummel, CL ;
Pacholski, ML ;
Swanek, FD ;
Ewing, AG ;
Winograd, N .
ANALYTICAL CHEMISTRY, 1997, 69 (13) :2225-2231
[10]   Controlling and measuring the interdependence of local properties in biomembranes [J].
D'Onofrio, TG ;
Hatzor, A ;
Counterman, AE ;
Heetderks, JJ ;
Sandel, MJ ;
Weiss, PS .
LANGMUIR, 2003, 19 (05) :1618-1623