Title :
Quantum Dot Probes for Monitoring Dynamic Cellular Response: Reporters of T Cell Activation
Author :
Warnement, Michael R. ; Faley, Shannon L. ; Wikswo, John P. ; Rosenthal, Sandra J.
Author_Institution :
Dept. of Chem., Vanderbilt Univ., Nashville, TN
Abstract :
Antibody-conjugated quantum dots (QDs) have been used to map the expression dynamics of the cytokine receptor interleukin-2 receptor-alpha (IL-2Ralpha) following Jurkat T cell activation. Maximal receptor expression was observed 48 h after activation, followed by a sharp decrease consistent with IL-2R internalization subsequent to IL-2 engagement. Verification of T cell activation and specificity of QD labeling were demonstrated using fluorescence microscopy, ELISA, and FACS analyses. These antibody conjugates provide a versatile means to rapidly determine cell state and interrogate membrane associated proteins involved in cell signaling pathways. Ultimately, incorporation with a microfluidic platform capable of simultaneously monitoring several cell signaling pathways will aid in toxin detection and discrimination
Keywords :
biomedical optical imaging; biomembranes; cellular biophysics; fluorescence; microfluidics; molecular biophysics; nanobiotechnology; nanocomposites; optical microscopy; proteins; quantum dots; 48 h; ELISA; FACS; Jurkat T cell activation; QD labeling; antibody-conjugated quantum dots; cell signaling pathway; cytokine receptor interleukin-2 receptor-alpha; dynamic cellular response monitoring; expression dynamics; fluorescence microscopy; maximal receptor expression; membrane associated proteins; microfluidic platform; quantum dot probes; toxin detection; Astrochemistry; Biomedical engineering; Biomembranes; Fluorescence; Monitoring; Optical imaging; Physiology; Probes; Quantum dots; US Department of Transportation; Cytokine expression; Jurkat T cells; interleukin-2 receptor (IL-2R); quantum dots (QDs); Cytokines; Humans; Jurkat Cells; Lymphocyte Activation; Microscopy, Fluorescence; Molecular Probe Techniques; Quantum Dots; Receptors, Cytokine; T-Lymphocytes;
Journal_Title :
NanoBioscience, IEEE Transactions on
DOI :
10.1109/TNB.2006.886573