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pubmed-article:19219023pubmed:abstractTextWe developed a new approach to bioluminescent T cell imaging using a membrane-anchored form of the Gaussia luciferase (GLuc) enzyme, termed extGLuc, which we could stably express in both mouse and human primary T cells. In vitro, extGLuc+ cells emitted significantly higher bioluminescent signal when compared to cells expressing GLuc, Renilla luciferase (RLuc) or membrane-anchored RLuc (extRLuc). In vivo, mouse extGLuc+ T cells showed higher bioluminescent signal when compared to GLuc+ and RLuc+ T cells. Application of this imaging approach to human T cells genetically modified to express tumor-specific chimeric antigen receptors (CARs) enabled us to show in vivo CAR-mediated T cell accumulation in tumor, T cell persistence over time and concomitant imaging of T cells and tumor cells modified to express firefly luciferase. This sensitive imaging technology has application to many in vivo cell-based studies in a wide array of mouse models.lld:pubmed
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pubmed-article:19219023pubmed:dateRevised2011-5-16lld:pubmed
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pubmed-article:19219023pubmed:articleTitleSensitive in vivo imaging of T cells using a membrane-bound Gaussia princeps luciferase.lld:pubmed
pubmed-article:19219023pubmed:affiliationDepartment of Radiology, Memorial Sloan Kettering Cancer Center (MSKCC), 1275 York Avenue, New York, New York 10021, USA.lld:pubmed
pubmed-article:19219023pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19219023pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
pubmed-article:19219023pubmed:publicationTypeResearch Support, N.I.H., Extramurallld:pubmed
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