Use of TIRF to Monitor T-Lymphocyte Membrane Dynamics with Submicrometer and Subsecond Resolution

• Published in: Cellular and molecular bioengineering Vol. 8; no. 1; pp. 178 - 186
• Main Authors: Brodovitch, Alexandre, Limozin, Laurent, Bongrand, Pierre, Pierres, Anne
• Format: Journal Article
• Language: English
• Published: Boston Springer US 01.03.2015; Springer Nature B.V; Spinger (en ligne) / BMES (imprimé)
• Subjects: Amplitudes; Antigens; Bioengineering; Biological and Medical Physics; Biomaterials; Biomedical Engineering and Bioengineering; Biomedical Engineering/Biotechnology; Biophysics; Cell Biology; Engineering; Fluorescence; Fluorescence microscopy; Interference; Life Sciences; Ligands; Lymphocytes; Membranes; Microscopy; Receptors; Reflection; Antigen detection; T-lymphocyte; Membrane movement; Total internal reflection fluorescence; Interface; Microvilli; Total internal reflection; fluorescence
• ISSN: 1865-5025; 1865-5033
• DOI: 10.1007/s12195-014-0361-8

A key step of adaptive immune responses is the T lymphocyte capacity to detect the presence of foreign antigens on specialized cells with high speed and specificity during contacts lasting a few minutes. Much evidence suggests that there is a deep link between the lifetime of molecular interactions between T cell receptors and ligands and T cell activation, but the precise mechanisms of bond formation and dissociation remain incompletely understood. Previous experiments done with interference reflection microscopy/reflection interference contrast microscopy disclosed transverse motions with several nanometer average amplitude of micrometer size membrane zones. More recently, total internal reflection fluorescence microscopy was used to show that the initial interaction between primary T lymphocytes and model surfaces involved the tip of microvilli (typically 0.2  µ m 2 area) generating apparent contacts of a few seconds that allowed cells to detect ligands of their membrane receptors. Here we show that these microvilli displayed minimal lateral displacements but quantitative fluorescence measurement suggested the occurrence of spontaneous transverse fluctuations of order of 67 nm amplitude during 1-s observation periods. This may play a major role in membrane receptor engagement and ensuing signal generation.