Veni, Vidi, Vici: In Vivo Molecular Imaging of Immune Response

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Veni, Vidi, Vici: In Vivo Molecular Imaging of Immune Response Shimon Gross, Britney L. Moss, David Piwnica-Worms  Immunity  Volume 27, Issue 4, Pages 533-538 (October 2007) DOI: 10.1016/j.immuni.2007.10.006 Copyright © 2007 Elsevier Inc. Terms and Conditions

Figure 1 Selected Examples of Molecular Imaging Strategies to Investigate Immune Response In Vivo (A and B) Imaging innate and adaptive immunity with injectable probes. (A) γ-scintigraphic images acquired at the indicated times after injection of 111In-DPC11870 (radiolabeled leukotriene antagonist) in a rabbit with acute colitis. Note the strong intestinal signal emitted as soon as 1–2 hr after administration of the probe (arrows) (reprinted by permission of the Society of Nuclear Medicine from van Eerd et al., 2004). (B) PET imaging after injection of 64Cu-labeled anti-glucose-6-phosphate-isomerase (GPI) IgG (left) or control IgG (right). Note the substantial accumulation of anti-GPI IgG in the joints (arrows) (adapted by permission from Macmillan Publishers Ltd: Nature Immunology [Wipke et al., 2002]). (C) Dynamic imaging of single immune cell interactions in vivo with fluorescent reporters and 2-photon intravital microscopy. Time-lapse images of a transient interaction between a GFP-tagged B cell and a CFP-tagged T cell in the dark zone of the germinal center (GC) in an intact lymph node in vivo (from Allen et al., 2007; reprinted with permission from AAAS). (D) Visualizing transcriptional activity in vivo by expression of an imaging reporter gene. By bioluminescence imaging (BLI), global Smad2 and Smad3 transcriptional activity was measured in pSBE→FLuc pan-expressing mice upon treatment with LPS (reprinted from Lin et al., 2005). (E) Imaging immune-mediated signaling cascades in real-time with post-translationally modified fusion reporters (induced protein degradation and stabilization). BLI of bortezomib-mediated modulation of LPS-induced IKK activity in vivo. A reporter of IKK activity (IκBα-FLuc) was delivered to hepatocytes by hydrodynamic somatic gene-transfer techniques. Mice were then imaged after the indicated treatments. Note that bortezomib not only abrogated LPS-induced activation of IKK (degradation of IκBα-FLuc), but actually promoted reporter accumulation, consistent with inhibition of both ligand-induced degradation and basal turnover of IκBα (reprinted by permission from Macmillan Publishers Ltd: Nature Methods [Gross and Piwnica-Worms, 2005a]). Immunity 2007 27, 533-538DOI: (10.1016/j.immuni.2007.10.006) Copyright © 2007 Elsevier Inc. Terms and Conditions