A New Type of Membrane Raft-Like Microdomains and Their Possible Involvement in TCR Signaling

• Published in: The Journal of immunology (1950) Vol. 184; no. 7; pp. 3689 - 3696
• Main Authors: Otahal, Pavel, Angelisova, Pavla, Hrdinka, Matous, Brdicka, Tomas, Novak, Petr, Drbal, Karel, Horejsi, Vaclav
• Format: Journal Article
• Language: English
• Published: United States Am Assoc Immnol 01-04-2010
• Subjects: Adaptor Proteins, Signal Transducing - immunology; Adaptor Proteins, Signal Transducing - metabolism; Humans; Jurkat Cells; Lymphocyte Activation - immunology; Membrane Microdomains - chemistry; Membrane Microdomains - immunology; Membrane Proteins - chemistry; Membrane Proteins - immunology; Membrane Proteins - isolation & purification; Membrane Proteins - metabolism; Receptors, Antigen, T-Cell - immunology; Receptors, Antigen, T-Cell - metabolism; Signal Transduction - immunology; T-Lymphocytes - chemistry; T-Lymphocytes - immunology; T-Lymphocytes - metabolism
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.0902075

Membrane rafts and signaling molecules associated with them are thought to play important roles in immunoreceptor signaling. Rafts differ in their lipid and protein compositions from the rest of the membrane and are relatively resistant to solubilization by Triton X-100 or similar detergents, producing buoyant, detergent-resistant membranes (DRMs) that can be isolated by density gradient ultracentrifugation. One of the key signaling molecules present in T cell DRMs is the transmembrane adaptor protein LAT (linker for activation of T cells). In contrast to previous results, a recent study demonstrated that a LAT construct not present in the buoyant DRMs is fully able to support TCR signaling and development of T cells in vivo. This finding caused doubts about the real physiological role of rafts in TCR signaling. In this study, we demonstrate that these results can be explained by the existence of a novel type of membrane raft-like microdomains, producing upon detergent solubilization "heavy DRMs" containing a number of membrane molecules. At a moderate level of expression, LAT supported TCR signaling more efficiently than constructs targeted to the microdomains producing heavy DRMs or to nonraft membrane. We suggest that different types of membrane microdomains provide environments regulating the functional efficiencies of signaling molecules present therein.