Nanoscale increases in CD2-CD48-mediated intermembrane spacing decrease adhesion and reorganize the immunological synapse.

Journal article

The relationship between intermembrane spacing, adhesion efficiency, and lateral organization of adhesion receptors has not been established for any adhesion system. We have utilized the CD2 ligand CD48 with two (wild type CD48 (CD48-WT)), four (CD48-CD2), or five (CD48-CD22) Ig-like domains. CD48-WT was 10-fold more efficient in mediating adhesion than CD48-CD2 or CD48-CD22. Electron tomography of contact areas with planar bilayers demonstrated average intermembrane spacing of 12.8 nm with CD48-WT, 14.7 nm with CD48-CD2, and 15.6 nm with CD48-CD22. Both CD48-CD2 and CD48-CD22 chimeras segregated completely from CD48-WT in mixed contact areas. In contrast, CD48-CD2 and CD48-CD22 co-localized when mixed contacts were formed. Confocal imaging of immunological synapses formed between primary T lymphocytes and Chinese hamster ovary cells presenting major histocompatibility complex-peptide complexes, and different forms of CD48 demonstrated that CD48-CD2 and CD48-CD22 induce an eccentric CD2/T cell antigen receptor cluster. We propose that this reorganization of the immunological synapse sequesters the T cell antigen receptor in a location where it cannot interact with its ligand and dramatically reduces T cell sensitivity.

Authors: Milstein, O; Tseng, S; Starr, T; Llodra, J; Nans, A

• Publication status: Published
• Journal: Journal of biological chemistry
• Volume: 283
• Issue: 49
• Pages: 34414-34422
• Publication date: 2008-12-01
• DOI: 10.1074/jbc.m804756200
• EISSN: 1083-351X
• ISSN: 0021-9258
• Language: English
• Keywords: Antigens, CD2; Sialic Acid Binding Ig-like Lectin 2; Immunological Synapses; CHO Cells; Antigens, CD; Flow Cytometry; Cricetinae; Cell Proliferation; Microscopy, Fluorescence; Animals; Cell Adhesion; Cricetulus; Mice; Electron Microscope Tomography; T-Lymphocytes