| Literature DB >> 28255716 |
Rachel Ambler1, Xiangtao Ruan2, Robert F Murphy3,4,5,6, Christoph Wülfing7.
Abstract
Three-dimensional live cell imaging of the interaction of T cells with antigen-presenting cells (APCs) visualizes the subcellular distributions of signaling intermediates during T cell activation at thousands of resolved positions within a cell. These information-rich maps of local protein concentrations are a valuable resource in understanding T cell signaling. Here, we describe a protocol for the efficient acquisition of such imaging data and their computational processing to create four-dimensional maps of local concentrations. This protocol allows quantitative analysis of T cell signaling as it occurs inside live cells with resolution in time and space across thousands of cells.Entities:
Keywords: Computational image analysis; Immunological synapse; Live cell imaging; Spatiotemporal distributions; T cell activation
Mesh:
Year: 2017 PMID: 28255716 PMCID: PMC5338467 DOI: 10.1007/978-1-4939-6881-7_25
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745