Microplate cell-retaining methodology for high-content analysis of individual non-adherent unanchored cells in a population

被引:20
作者
Deutsch, Assaf [1 ]
Zurgil, Naomi [1 ]
Hurevich, Ihar [1 ]
Shafran, Yana [1 ]
Afrimzon, Elena [1 ]
Lebovich, Pnina [1 ]
Deutsch, Mordechai [1 ]
机构
[1] Bar Ilan Univ, Dept Phys, Biophys Interdisciplinary Jerome Schottenstein Ct, IL-52900 Ramat Gan, Israel
关键词
Microtiter plate Cell Retainer (MCR); individual non-adherent non-anchored cells; correlative high-content functional kinetic and post-fixation analysis; individual cell transmitted light and fluorescence detection;
D O I
10.1007/s10544-006-9143-y
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
A high throughput Microtiter plate Cell Retainer (MCR) has been developed to enable, for the first time, high-content, time-dependent analysis of the same single non-adherent and non-anchored cells in a large cell population, while bio-manipulating the cells. The identity of each cell in the investigated population is secured, even during bio-manipulation, by cell retention in a specially designed concave microlens, acting as a picoliter well (PW). The MCR technique combines micro-optical features and microtiter plate methodology. The array of PWs serves as the bottom of a microtiter plate, fitted with a unique flow damper element. The latter enables rapid fluid exchange without dislodging the cells from their original PWs, thus maintaining the cells' identity. Loading cell suspensions and reagents into the MCR is performed by simple pouring, followed by gravitational sedimentation and settling of cells into the PWs. Cell viability and cell division within the MCR were shown to be similar to those obtained under similar conditions in a standard microtiter plate. The efficiency of single cell occupancy in the MCR exceeded 90%. No cell dislodging was observed when comparing images before and after bio-manipulations (rinsing, staining, etc.). The MCR permits the performance of kinetic measurements on an individual cell basis. Data acquisition is governed by software, controlling microscope performance, stage position and image acquisition and analysis. The PW's unique micro-optical features enable rapid, simultaneous signal analysis of each individual cell, bypassing lengthy image analysis.
引用
收藏
页码:361 / 374
页数:14
相关论文
共 46 条
[1]
Optical Imaging fiber-based single live cell arrays: A high-density cell assay platform [J].
Biran, I ;
Walt, DR .
ANALYTICAL CHEMISTRY, 2002, 74 (13) :3046-3054
[2]
Micromachining sensors for electrochemical measurement in subnanoliter volumes [J].
Bratten, CDT ;
Cobbold, PH ;
Cooper, JM .
ANALYTICAL CHEMISTRY, 1997, 69 (02) :253-258
[3]
Quantitative chemical analysis of single cells [J].
Cannon, DM ;
Winograd, N ;
Ewing, AG .
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2000, 29 :239-263
[4]
Continuous cell introduction for the analysis of individual cells by capillary electrophoresis [J].
Chen, SJ ;
Lillard, SJ .
ANALYTICAL CHEMISTRY, 2001, 73 (01) :111-118
[5]
Microfabricated platform for studying stem cell fates [J].
Chin, VI ;
Taupin, P ;
Sanga, S ;
Scheel, J ;
Gage, FH ;
Bhatia, SN .
BIOTECHNOLOGY AND BIOENGINEERING, 2004, 88 (03) :399-415
[6]
CLERVAL R, 2000, BIOWORLD, V6, P24
[7]
Regulated cell-to-cell variation in a cell-fate decision system [J].
Colman-Lerner, A ;
Gordon, A ;
Serra, E ;
Chin, T ;
Resnekov, O ;
Endy, D ;
Pesce, CG ;
Brent, R .
NATURE, 2005, 437 (7059) :699-706
[8]
High-throughput methods for culturing microorganisms in very-low-nutrient media yield diverse new marine isolates [J].
Connon, SA ;
Giovannoni, SJ .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2002, 68 (08) :3878-3885
[9]
APPARATUS FOR HIGH-PRECISION REPETITIVE SEQUENTIAL OPTICAL MEASUREMENT OF LIVING CELLS [J].
DEUTSCH, M ;
WEINREB, A .
CYTOMETRY, 1994, 16 (03) :214-226
[10]
The use of microscale processing technologies for quantification of biocatalytic Baeyer-Villiger oxidation kinetics [J].
Doig, SD ;
Pickering, SCR ;
Lye, GJ ;
Woodley, JM .
BIOTECHNOLOGY AND BIOENGINEERING, 2002, 80 (01) :42-49