Quantitative phase microscopy: a new tool for measurement of cell culture growth and confluency in situ

被引:35
作者
Curl, CL
Harris, T
Harris, PJ
Allman, BE
Bellair, CJ
Stewart, AG
Delbridge, LMD [1 ]
机构
[1] Univ Melbourne, Dept Physiol, Melbourne, Vic 3010, Australia
[2] Univ Melbourne, Dept Pharmacol, Melbourne, Vic 3010, Australia
[3] Univ Melbourne, Sch Phys, Melbourne, Vic 3010, Australia
来源
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY | 2004年 / 448卷 / 04期
关键词
quantitative phase microscopy; cell culture; confluency; image analysis; airway smooth muscle cells; optical thickness;
D O I
10.1007/s00424-004-1248-7
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Quantitative phase microscopy (QPM) is a recently developed computational approach that provides quantitative phase measurements of specimen images obtained under bright-field conditions without phase- or interference-contrast optics. To perform QPM, an in-focus bright-field image is acquired, together with one positive and one negative de-focus image. An algorithm is then applied to produce a specimen phase map. In this investigation we demonstrate that manipulation of the phase map intensity histogram using novel, non-subjective thresholding and segmentation methods provides enhanced delineation of cells in culture. QPM was utilised to measure the growth behaviour of cultured airway smooth muscle cells over a 92-h period. There was a high degree of correlation between parallel QPM-derived confluency measurements and haemocytometry-derived counts of airway smooth muscle cells over this time period. Using QPM, translucent cells can be visualised with improved cell boundary definition allowing precise and reproducible measurements of cell culture confluency. Quantitative phase imaging provides a rapid, optically simple and non-destructive approach for measurement of cellular morphology. Further development of the QPM-based analysis methodology has the potential to provide even more refined measures of cellular growth.
引用
收藏
页码:462 / 468
页数:7
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