NSOM/QD-based visualization of GM1 serving as platforms for TCR/CD3 mediated T-cell activation

Biomed Res Int. 2013:2013:276498. doi: 10.1155/2013/276498. Epub 2013 Oct 30.

Abstract

Direct molecular imaging of nanoscale relationship between T-cell receptor complexes (TCR/CD3) and gangliosidosis GM1 before and after T-cell activation has not been reported. In this study, we made use of our expertise of near-field scanning optical microscopy(NSOM)/immune-labeling quantum dots- (QD-)based dual-color imaging system to visualize nanoscale profiles for distribution and organization of TCR/CD3, GM1, as well as their nanospatial relationship and their correlation with PKC θ signaling cascade during T-cell activation. Interestingly, after anti-CD3/anti-CD28 Ab co-stimulation, both TCR/CD3 and GM1 were clustered to form nanodomains; moreover, all of TCR/CD3 nanodomains were colocalized with GM1 nanodomains, indicating that the formation of GM1 nanodomains was greatly correlated with TCR/CD3 mediated signaling. Specially, while T-cells were pretreated with PKC θ signaling inhibitor rottlerin to suppress IL-2 cytokine production, no visible TCR/CD3 nanodomains appeared while a lot of GM1 nanodomains were still observed. However, while T-cells are pretreated with PKCα β signaling inhibitor GÖ6976 to suppress calcium-dependent manner, all of TCR/CD3 nanodomains were still colocalized with GM1 nanodomains. These findings possibly support the notion that the formation of GM1 nanodomains indeed serves as platforms for the recruitment of TCR/CD3 nanodomains, and TCR/CD3 nanodomains are required for PKCθ signaling cascades and T-cell activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD3 Complex / metabolism*
  • G(M1) Ganglioside / metabolism*
  • Humans
  • Interleukin-2 / metabolism
  • Isoenzymes / metabolism
  • Lymphocyte Activation / immunology*
  • Microscopy / methods*
  • Optical Imaging
  • Protein Kinase C / metabolism
  • Protein Kinase C-theta
  • Quantum Dots / metabolism*
  • Receptors, Antigen, T-Cell / metabolism*
  • Signal Transduction
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / immunology*

Substances

  • CD3 Complex
  • Interleukin-2
  • Isoenzymes
  • Receptors, Antigen, T-Cell
  • G(M1) Ganglioside
  • PRKCQ protein, human
  • Protein Kinase C
  • Protein Kinase C-theta