Imaging approaches for monitoring three-dimensional cell and tissue culture systems

被引:10
作者
Hilzenrat, Geva [1 ,2 ]
Gill, Emma T. [1 ,2 ]
McArthur, Sally L. [1 ,2 ]
机构
[1] Swinburne Univ Technol, Sch Sci Comp & Engn Technol, Bioengn Engn Grp, Hawthorn, Vic, Australia
[2] Commonwealth Sci & Ind Res Org CSIRO, Biomed Mfg, Clayton, Vic, Australia
关键词
auto-fluorescence; coherent anti-stokes Raman scattering spectroscopy; fluorescence lifetime imaging; fluorescence microscopy; Imaging 3D cell culture; multiphoton microscopy; optical coherence tomography; photoacoustic imaging; photothermal imaging; second harmonic generation; stimulated Raman spectroscopy imaging; tissue bioengineering; 2ND-HARMONIC GENERATION MICROSCOPY; FREE PHOTOACOUSTIC MICROSCOPY; OPTICAL COHERENCE TOMOGRAPHY; RAMAN-SCATTERING MICROSCOPY; SPECTRAL PHASOR ANALYSIS; IN-VIVO; FLUORESCENCE LIFETIME; MULTIPHOTON MICROSCOPY; QUANTITATIVE-ANALYSIS; REDOX RATIO;
D O I
10.1002/jbio.202100380
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The past decade has seen an increasing demand for more complex, reproducible and physiologically relevant tissue cultures that can mimic the structural and biological features of living tissues. Monitoring the viability, development and responses of such tissues in real-time are challenging due to the complexities of cell culture physical characteristics and the environments in which these cultures need to be maintained in. Significant developments in optics, such as optical manipulation, improved detection and data analysis, have made optical imaging a preferred choice for many three-dimensional (3D) cell culture monitoring applications. The aim of this review is to discuss the challenges associated with imaging and monitoring 3D tissues and cell culture, and highlight topical label-free imaging tools that enable bioengineers and biophysicists to non-invasively characterise engineered living tissues.
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页数:27
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