Visualizing Surface T-Cell Receptor Dynamics Four-Dimensionally Using Lattice Light-Sheet Microscopy

被引:5
|
作者
Rosenberg, Jillian [1 ]
Huang, Jun [1 ,2 ]
机构
[1] Univ Chicago, Comm Canc Biol, Chicago, IL 60637 USA
[2] Univ Chicago, Pritzker Sch Mol Engn, Chicago, IL 60637 USA
来源
基金
美国国家科学基金会;
关键词
Biochemistry; Issue; 155; lattice light-sheet microscopy; immunology; T-cell receptor; imaging; tracking; dynamics; FLUORESCENCE; RECONSTRUCTION; LIMIT;
D O I
10.3791/59914
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The signaling and function of a cell are dictated by the dynamic structures and interactions of its surface receptors. To truly understand the structure-function relationship of these receptors in situ, we need to visualize and track them on the live cell surface with enough spatiotemporal resolution. Here we show how to use recently developed Lattice Light-Sheet Microscopy (LLSM) to image T-cell receptors (TCRs) four-dimensionally (4D, space and time) at the live cell membrane. T cells are one of the main effector cells of the adaptive immune system, and here we used T cells as an example to show that the signaling and function of these cells are driven by the dynamics and interactions of the TCRs. LLSM allows for 4D imaging with unprecedented spatiotemporal resolution. This microscopy technique therefore can be generally applied to a wide array of surface or intracellular molecules of different cells in biology.
引用
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页数:8
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