Showing 1 - 11 results of 11 for search '"micronation"', query time: 0.06s Refine Results
  1. 1

    Influence of receptor lateral mobility on adhesion strengthening between membranes containing LFA-3 and CD2. by Chan, P, Lawrence, M, Dustin, M, Ferguson, L, Golan, D, Springer, T

    Published 1991
    “…Kinetic measurements demonstrated an influence of contact time on the strength of adhesion to the GPI isoform at lower site densities (25-50 sites/microns2), showing that the mobility of LFA-3 is important in adhesion strengthening. …”
    Journal article
  2. 2

    Motility and ultrastructure of large granular lymphocytes on lipid bilayers reconstituted with adhesion receptors LFA-1, ICAM-1, and two isoforms of LFA-3. by Carpén, O, Dustin, M, Springer, T, Swafford, J, Beckett, L, Caulfield, J

    Published 1991
    “…Here we have studied the motility and ultrastructure of large granule lymphocyte (LGL) on lipid bilayers containing purified LFA-1, ICAM-1, and the transmembrane and glycophosphatidylinositol isoforms of LFA-3. LGLs moved at 8 microns/min on ICAM-1 but poorly (less than 1 microns/min) on its receptor pair LFA-1. …”
    Journal article
  3. 3

    Signaling at neuro/immune synapses. by Dustin, M

    Published 2012
    “…The discovery of phosphatase micro-exclusion from signaling elements in immunological synapses and innate phagocytic synapses define a common functional unit at a common sub-micron scale across synapse types. Bundling of information from multiple antigen receptor microclusters by an immunological synapse has parallels to bundling of multiple synaptic inputs into a single axonal output by neurons, allowing integration and coincidence detection. …”
    Journal article
  4. 4

    Signaling microdomains in T cells. by Choudhuri, K, Dustin, M

    Published 2010
    “…Sub-micron scale signaling domains induced in the plasma membrane of cells are thought to play important roles in signal transduction. …”
    Journal article
  5. 5

    Membrane nanoclusters of FcγRI segregate from inhibitory SIRPα upon activation of human macrophages by Lopes, F, Bálint, Š, Valvo, S, Felce, J, Hessel, E, Dustin, M, Davis, D

    Published 2017
    “…Thus, a nanometer- and micron-scale reorganization of activating and inhibitory receptors occurs at the surface of human macrophages concurrent with signal integration.…”
    Journal article
  6. 6

    TCR-mediated adhesion of T cell hybridomas to planar bilayers containing purified MHC class II/peptide complexes and receptor shedding during detachment. by Dustin, M, Miller, J, Ranganath, S, Vignali, D, Viner, N, Nelson, C, Unanue, E

    Published 1996
    “…T cell recognition of foreign Ag/MHC class II complexes is sensitive down to approximately 100 complexes per cell or approximately 0.2 complexes/micron2. To better understand the physical basis of the recognition stage of Ag presentation, we examined adhesion of the lysozyme- specific T cell hybridoma, 3A9, to artificial bilayers containing covalent MHC class II/peptide complexes or adhesion molecules. …”
    Journal article
  7. 7

    Micromanipulation of adhesion of phorbol 12-myristate-13-acetate-stimulated T lymphocytes to planar membranes containing intercellular adhesion molecule-1. by Tözeren, A, Mackie, L, Lawrence, M, Chan, P, Dustin, M, Springer, T

    Published 1992
    “…The physical strength of adhesion between a PMA-stimulated T lymphocyte and a planar membrane containing 1,000 ICAM-1 molecules/micron 2 was comparable to the strength of adhesion between a cytotoxic T cell and its target cell. …”
    Journal article
  8. 8

    Visualization of CD2 interaction with LFA-3 and determination of the two-dimensional dissociation constant for adhesion receptors in a contact area. by Dustin, M, Ferguson, L, Chan, P, Springer, T, Golan, D

    Published 1996
    “…The two-dimensional Kd for the CD2/LFA-3 interaction was 21 molecules/microns 2, which is lower than the surface densities of CD2 on T cells and LFA-3 on most target or stimulator cells. …”
    Journal article
  9. 9

    Micromanipulation of adhesion of a Jurkat cell to a planar bilayer membrane containing lymphocyte function-associated antigen 3 molecules. by Tözeren, A, Sung, K, Sung, L, Dustin, M, Chan, P, Springer, T, Chien, S

    Published 1992
    “…In particular, we investigated the adhesion between a Jurkat cell expressing CD2 and a glass-supported planar bilayer containing either the glycosyl-phosphatidylinositol (GPI) or the transmembrane (TM) isoform of the counter-receptor lymphocyte function-associated antigen 3 (LFA-3) at a concentration of 1,000 molecules/microns 2. In response to the pipette force the Jurkat cells that adhered to the planar bilayer containing the GPI isoform of LFA-3 underwent extensive elongation. …”
    Journal article
  10. 10

    Regulation of locomotion and cell-cell contact area by the LFA-1 and ICAM-1 adhesion receptors. by Dustin, M, Carpen, O, Springer, T

    Published 1992
    “…B lymphoblasts formed a large contact area and crawled rapidly (up to 25 microns/min) on planar bilayers bearing ICAM-1. In contrast, these cells attached to planar bilayers bearing LFA-1 through a fixed point about which the cells actively pivoted, using a single stalk-like projection. …”
    Journal article
  11. 11

    Rosetting of human T lymphocytes with sheep and human erythrocytes. Comparison of human and sheep ligand binding using purified E receptor. by Selvaraj, P, Dustin, M, Mitnacht, R, Hünig, T, Springer, T, Plunkett, M

    Published 1987
    “…Human and sheep E have surface areas of 145 and 54 micron 2, respectively. The 3.2- to 5.6-fold higher ligand density on sheep E appears to account for the ability of sheep but not human E to rosette with certain types of human T lymphocytes.…”
    Journal article