Artefact reduction for cell migration visualization using spectral domain optical coherence tomography

被引:12
作者
Hofer, Bernd [1 ,2 ,3 ]
Povazay, Boris [1 ,2 ]
Hermann, Boris [1 ,2 ]
Rey, Sara M. [2 ]
Kajic, Vedran [2 ]
Tumlinson, Alexandre [2 ]
Powell, Kate [2 ]
Matz, Gerald [3 ]
Drexler, Wolfgang [1 ,2 ]
机构
[1] Med Univ Vienna, Ctr Med Phys & Biomed Engn, A-1090 Vienna, Austria
[2] Cardiff Univ, Sch Optometry & Vis Sci, Biomed Imaging Grp, Cardiff CF24 4LU, S Glam, Wales
[3] Vienna Univ Technol, Inst Commun & Radiofrequency Engn, A-1040 Vienna, Austria
基金
奥地利科学基金会;
关键词
tomography; optical coherence; microscopy; cell physiological phenomena; image processing; computer-assisted; imaging; three-dimensional; biomedical engineering; IN-VIVO; MULTIPHOTON MICROSCOPY; PHASE MICROSCOPY; HIGH-SPEED; RESOLUTION; DYNAMICS; IMAGES; OCT;
D O I
10.1002/jbio.201000109
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Visualization of cell migration during chemotaxis using spectral domain optical coherence tomography (OCT) requires non-standard processing techniques. Stripe artefacts and camera noise floor present in OCT data prevent detailed computer-assisted reconstruction and quantification of cell locomotion. Furthermore, imaging artefacts lead to unreliable results in automated texture based cell analysis. Here we characterize three pronounced artefacts that become visible when imaging sample structures with high dynamic range, e. g. cultured cells: (i) time-varying fixed-pattern noise; (ii) stripe artefacts generated by background estimation using tomogram averaging; (iii) image modulations due to spectral shaping. We evaluate techniques to minimize the above mentioned artefacts using an 800 nm optical coherence microscope. Effect of artefact reduction is shown exemplarily on two cell cultures, i.e. Dictyostelium on nitrocellulose substrate, and retinal ganglion cells (RGC-5) cultured on a glass coverslip. Retinal imaging also profits from the proposed processing techniques.
引用
收藏
页码:355 / 367
页数:13
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