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Multiplex analysis of inflammatory signaling pathways using a high-content imaging system
Author(s): Bertelsen M (Bertelsen, Malene)
Source: MEASURING BIOLOGICAL RESPONSES WITH AUTOMATED MICROSCOPY   Book Series: METHODS IN ENZYMOLOGY    Volume: 414    Pages: 348-363    Published: 2006  
Times Cited: 5     References: 20     
Abstract: This chapter describes a robust high-content cellular screening assay to simultaneously analyze the spatiotemporal activation of three different kinase-associated signaling pathways involving NF-kappa B, JNK, and p38, all of which are closely implicated in proliferative and proinflammatory responses. Signal transduction is dependent on the translocation of NF-kappa B p65 and phosphorylated c-Jun and p38 from the cytosol to the nucleus, and fluorescent immunolabeling was used to monitor changes in their cellular distribution. Cellular screening, data acquisition, and data interpretation were conducted on the ArrayScan HCS Reader (Cellomics Inc., Pittsburgh, PA). Assay adaptation to various cellular systems is feasible when sufficient separation of the nuclear and cytosolic compartment can be achieved and if cell adhesion properties permit proper attachment to the culture plates. Substitution of NF-kappa B p65 and phosphorylated forms of c-Jun and p38 as targets to analyze other translocating components is possible and is limited primarily by antibody specificity and the risk of fluorescent bleed-through between emission channels. Because assay validity is particularly confounded by inadequate spectral separation of the detection dyes in multicolor labeling assays, means of eliminating or counterbalancing staining artifacts are illustrated. Also, protocol parameter settings important for imaging and image processing are described, including object identification, image exposure settings, separation of cytosolic and nuclear regions, number of cells sufficient for analysis, and the use of gating thresholds critical for cell sorting and subpopulation analysis. This assay is a useful tool to investigate the interplay between signaling pathways and the mode of action, potency, and selectivity of compound inhibition of specific target molecules in a cellular context.
Document Type: Review
Language: English
Reprint Address: Bertelsen, M (reprint author), AstraZeneca R&D, Dept Sci Biol, Lund, Sweden
Addresses:
1. AstraZeneca R&D, Dept Sci Biol, Lund, Sweden
Publisher: ELSEVIER ACADEMIC PRESS INC, 525 B STREET, SUITE 1900, SAN DIEGO, CA 92101-4495 USA
Subject Category: Biochemical Research Methods; Biochemistry & Molecular Biology
IDS Number: BFN15
ISSN: 0076-6879
DOI: 10.1016/S0076-6879(06)14020-3
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