Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Results from live-cell microscopy suggest that the behaviour of isolated components of the T-cell activation machinery in vitro does not represent the reality inside cells. Understanding the cellular-scale dynamics of microcluster migration can only be accomplished by in situ observation. Developments in 'super-resolution' microscopy have permitted investigators to move beyond tracking the movements of individual molecules, allowing the recognition of protein islands and nanodomains present in quiescent and active T cells. Many high-resolution techniques have their own susceptibilities to artefacts, so it is important to take a multifaceted approach to confirm results. A major challenge for the future will be to integrate all the new information into a coherent model of antigen recognition and T-cell activation.

Original publication

DOI

10.1111/j.1365-2567.2011.03537.x

Type

Journal article

Journal

Immunology

Publication Date

03/2012

Volume

135

Pages

198 - 206

Keywords

Animals, Fluorescence Resonance Energy Transfer, Humans, In Vitro Techniques, Kinetics, Lipid Bilayers, Lymphocyte Activation, Major Histocompatibility Complex, Microscopy, Fluorescence, Receptors, Antigen, T-Cell, T-Lymphocytes