Imaging red blood cell dynamics by quantitative phase microscopy

被引:213
作者
Popescu, Gabriel [1 ]
Park, YoungKeun [1 ]
Choi, Wonshik [1 ]
Dasari, Ramachandra R. [1 ]
Feld, Michael S. [1 ]
Badizadegan, Kamran [1 ,2 ,3 ]
机构
[1] MIT, George R Harrison Spect Lab, Cambridge, MA 02139 USA
[2] Harvard Univ, Sch Med, Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Div Hlth Sci & Technol, Boston, MA 02114 USA
关键词
phase microscopy; quantitative microscopy; red blood cells; cell mechanics;
D O I
10.1016/j.bcmd.2008.01.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Red blood cells (RBCs) play a crucial role in health and disease, and structural and mechanical abnormalities of these cells have been associated with important disorders such as Sickle cell disease and hereditary cytoskeletal abnormalities. Although several experimental methods exist for analysis of RBC mechanical properties, optical methods stand out as they enable collecting mechanical and dynamic data from live cells without physical contact and without the need for exogenous contrast agents. In this report, we present quantitative phase microscopy techniques that enable imaging RBC membrane fluctuations with nanometer sensitivity at arbitrary time scales from milliseconds to hours. We further provide a theoretical framework for extraction of membrane mechanical and dynamical properties using time series of quantitative phase images. Finally, we present an experimental approach to extend quantitative phase imaging to 3-dimensional space using tomographic methods. By providing non-invasive methods for imaging mechanics of live cells, these novel techniques provide an opportunity for high-throughput analysis and study of RBC mechanical properties in health and disease. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:10 / 16
页数:7
相关论文
共 53 条
[31]   High-resolution quantitative phase-contrast microscopy by digital holography [J].
Mann, CJ ;
Yu, LF ;
Lo, CM ;
Kim, MK .
OPTICS EXPRESS, 2005, 13 (22) :8693-8698
[32]   Digital holographic microscopy: a noninvasive contrast imaging technique allowing quantitative visualization of living cells with subwavelength axial accuracy [J].
Marquet, P ;
Rappaz, B ;
Magistretti, PJ ;
Cuche, E ;
Emery, Y ;
Colomb, T ;
Depeursinge, C .
OPTICS LETTERS, 2005, 30 (05) :468-470
[33]  
Mills J P, 2004, Mech Chem Biosyst, V1, P169
[34]  
NASH GB, 1993, BIORHEOLOGY, V30, P397
[35]   Quantitative optical microscope with enhanced resolution using a pixelated liquid crystal spatial light modulator [J].
Ng, AYM ;
See, CW ;
Somekh, MG .
JOURNAL OF MICROSCOPY, 2004, 214 :334-340
[36]   Noninterferometric phase imaging with partially coherent light [J].
Paganin, D ;
Nugent, KA .
PHYSICAL REVIEW LETTERS, 1998, 80 (12) :2586-2589
[37]   Fresnel particle tracing in three dimensions using diffraction phase microscopy [J].
Park, YongKeun ;
Popescu, Gabriel ;
Badizadegan, Kamran ;
Dasari, Ramachandra R. ;
Feld, Michael S. .
OPTICS LETTERS, 2007, 32 (07) :811-813
[38]   Diffraction phase and fluorescence microscopy [J].
Park, YongKeun ;
Popescu, Gabriel ;
Badizadegan, Kamran ;
Dasari, Ramachandra R. ;
Feld, Michael S. .
OPTICS EXPRESS, 2006, 14 (18) :8263-8268
[39]   Erythrocyte structure and dynamics quantified by Hilbert phase microscopy [J].
Popescu, G ;
Ikeda, T ;
Best, CA ;
Badizadegan, K ;
Dasari, RR ;
Feld, MS .
JOURNAL OF BIOMEDICAL OPTICS, 2005, 10 (06)
[40]   Diffraction phase microscopy for quantifying cell structure and dynamics [J].
Popescu, G ;
Ikeda, T ;
Dasari, RR ;
Feld, MS .
OPTICS LETTERS, 2006, 31 (06) :775-777