共 64 条
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
来源:
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.
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页码:198 / 206
页数:9
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