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4D electron microscopy of T cell activation.

Yue LuByung-Kuk YooAlphonsus H C NgJungwoo KimSinchul YeomJau TangMilo M LinAhmed H ZewailJames R Heath
Published in: Proceedings of the National Academy of Sciences of the United States of America (2019)
T cells can be controllably stimulated through antigen-specific or nonspecific protocols. Accompanying functional hallmarks of T cell activation can include cytoskeletal reorganization, cell size increase, and cytokine secretion. Photon-induced near-field electron microscopy (PINEM) is used to image and quantify evanescent electric fields at the surface of T cells as a function of various stimulation conditions. While PINEM signal strength scales with multiple of the biophysical changes associated with T cell functional activation, it mostly strongly correlates with antigen-engagement of the T cell receptors, even under conditions that do not lead to functional T cell activation. PINEM image analysis suggests that a stimulation-induced reorganization of T cell surface structure, especially over length scales of a few hundred nanometers, is the dominant contributor to these PINEM signal changes. These experiments reveal that PINEM can provide a sensitive label-free probe of nanoscale cellular surface structures.
Keyphrases
  • electron microscopy
  • label free
  • cell surface
  • high glucose
  • diabetic rats
  • high resolution
  • stem cells
  • drug induced
  • cell therapy
  • gene expression
  • bone marrow
  • endothelial cells
  • mesenchymal stem cells
  • stress induced