TY - CHAP
T1 - Current State-of-the-Art 3D Tissue Models and Their Compatibility with Live Cell Imaging
AU - Bardsley, Katie
AU - Deegan, Anthony J
AU - El Haj, Alicia
AU - Yang, Ying
PY - 2017/10
Y1 - 2017/10
N2 - Mammalian cells grow within a complex three-dimensional (3D) microenvironment where multiple cells are organized and surrounded by extracellular matrix (ECM). The quantity and types of ECM components, alongside cell-to-cell and cell-to-matrix interactions dictate cellular differentiation, proliferation and function in vivo. To mimic natural cellular activities, various 3D tissue culture models have been established to replace conventional two dimensional (2D) culture environments. Allowing for both characterization and visualization of cellular activities within possibly bulky 3D tissue models presents considerable challenges due to the increased thickness and subsequent light scattering features of such 3D models. In this chapter, state-of-the-art methodologies used to establish 3D tissue models are discussed, first with a focus on both scaffold-free and scaffold-based 3D tissue model formation. Following on, multiple 3D live cell imaging systems, mainly optical imaging modalities, are introduced. Their advantages and disadvantages are discussed, with the aim of stimulating more research in this highly demanding research area.
AB - Mammalian cells grow within a complex three-dimensional (3D) microenvironment where multiple cells are organized and surrounded by extracellular matrix (ECM). The quantity and types of ECM components, alongside cell-to-cell and cell-to-matrix interactions dictate cellular differentiation, proliferation and function in vivo. To mimic natural cellular activities, various 3D tissue culture models have been established to replace conventional two dimensional (2D) culture environments. Allowing for both characterization and visualization of cellular activities within possibly bulky 3D tissue models presents considerable challenges due to the increased thickness and subsequent light scattering features of such 3D models. In this chapter, state-of-the-art methodologies used to establish 3D tissue models are discussed, first with a focus on both scaffold-free and scaffold-based 3D tissue model formation. Following on, multiple 3D live cell imaging systems, mainly optical imaging modalities, are introduced. Their advantages and disadvantages are discussed, with the aim of stimulating more research in this highly demanding research area.
KW - Animals
KW - Cell Communication
KW - Cell Tracking/instrumentation
KW - Coculture Techniques
KW - Endothelial Cells/metabolism
KW - Extracellular Matrix/metabolism
KW - HCT116 Cells
KW - Humans
KW - Imaging, Three-Dimensional/instrumentation
KW - Mesenchymal Stromal Cells/metabolism
KW - Microscopy, Confocal/instrumentation
KW - Microscopy, Fluorescence/instrumentation
KW - Optical Imaging/instrumentation
KW - Tissue Engineering
KW - Tissue Scaffolds
KW - Tomography, X-Ray Computed/instrumentation
U2 - 10.1007/978-3-319-67358-5_1
DO - 10.1007/978-3-319-67358-5_1
M3 - Chapter
C2 - 29080127
SN - 978-3-319-67357-8
VL - 1035
T3 - Advances in Experimental Medicine and Biology
SP - 3
EP - 18
BT - Multi-Parametric Live Cell Microscopy of 3D Tissue Models
PB - Springer
ER -