Dissecting T-cell activation with high-resolution live-cell microscopy

被引:4
作者
Illingworth, Joseph J. [1 ]
van der Merwe, P. Anton [1 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国医学研究理事会;
关键词
immune synapse; photoactivated localization microscopy; stochastic optical reconstruction microscopy; super-resolution; TOCCSL; two-colour coincidence detection; STRUCTURED-ILLUMINATION MICROSCOPY; PLASMA-MEMBRANE MICRODOMAINS; IMMUNOLOGICAL SYNAPSE; SINGLE-MOLECULE; FLUORESCENCE MICROSCOPY; LOCALIZATION MICROSCOPY; RECEPTOR MICROCLUSTERS; STIMULATED-EMISSION; DIFFRACTION-LIMIT; STED MICROSCOPY;
D O I
10.1111/j.1365-2567.2011.03537.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Results from live-cell microscopy suggest that the behaviour of isolated components of the T-cell activation machinery in vitro does not represent the reality inside cells. Understanding the cellular-scale dynamics of microcluster migration can only be accomplished by in situ observation. Developments in super-resolution microscopy have permitted investigators to move beyond tracking the movements of individual molecules, allowing the recognition of protein islands and nanodomains present in quiescent and active T cells. Many high-resolution techniques have their own susceptibilities to artefacts, so it is important to take a multifaceted approach to confirm results. A major challenge for the future will be to integrate all the new information into a coherent model of antigen recognition and T-cell activation.
引用
收藏
页码:198 / 206
页数:9
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