Super-Resolution Imaging Approaches for Quantifying F-Actin in Immune Cells

被引:5
作者
Garlick, Evelyn [1 ,2 ,3 ]
Thomas, Steven G. [1 ,2 ,3 ]
Owen, Dylan M. [2 ,3 ,4 ,5 ]
机构
[1] Univ Birmingham, Inst Cardiovasc Sci, Coll Med & Dent Sci, Birmingham, W Midlands, England
[2] Univ Birmingham, Ctr Membrane Proteins & Receptors, Midlands, England
[3] Univ Nottingham, Midlands, England
[4] Univ Birmingham, Inst Immunol & Immunotherapy, Coll Med & Dent Sci, Birmingham, W Midlands, England
[5] Univ Birmingham, Sch Math, Coll Engn & Phys Sci, Birmingham, W Midlands, England
基金
英国生物技术与生命科学研究理事会;
关键词
actin; microscopy; super-resolution; fiber analysis; cytoskeleton; IMMUNOLOGICAL SYNAPSE; LOCALIZATION MICROSCOPY; GRANULE SECRETION; DYNAMICS; CYTOSKELETON; ACTIVATION; VISUALIZATION; LIFEACT; PROBES; BINDING;
D O I
10.3389/fcell.2021.676066
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Immune cells comprise a diverse set of cells that undergo a complex array of biological processes that must be tightly regulated. A key component of cellular machinery that achieves this is the cytoskeleton. Therefore, imaging and quantitatively describing the architecture and dynamics of the cytoskeleton is an important research goal. Optical microscopy is well suited to this task. Here, we review the latest in the state-of-the-art methodology for labeling the cytoskeleton, fluorescence microscopy hardware suitable for such imaging and quantitative statistical analysis software applicable to describing cytoskeletal structures. We also highlight ongoing challenges and areas for future development.</p>
引用
收藏
页数:10
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