Contact-induced redistribution of specific membrane components: local accumulation and development of adhesion.
Open Access
- 1 June 1986
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 102 (6) , 2185-2196
- https://doi.org/10.1083/jcb.102.6.2185
Abstract
We have used a model system to explore the importance of long-range lateral diffusion of membrane proteins in specific membrane-membrane adhesion. Single, cell-size phospholipid vesicles containing a dinitrophenyl (DNP)-lipid hapten were maneuvered into contact with rat basophilic leukemia (RBL) cells carrying fluorescent anti-DNP IgE in their cell-surface Fc epsilon receptors. Upon cell-vesicle contact the antibody molecules underwent a marked lateral redistribution, accumulating at the site of contact and becoming significantly depleted from noncontacting membrane. As assayed with a micropipette suction method, there was a time-dependent increase in the strength of cell-vesicle adhesion. This development of adhesion paralleled the kinetics of accumulation of the adhesion-mediating antibody molecules at the zone of membrane-membrane contact. Both adhesion and redistribution were absolutely dependent upon a specific interaction of the IgE with the hapten: No redistribution occurred when vesicles lacking the DNP hapten were pushed against IgE-armed RBL cells, and on cells bearing a 1:1 mixture of nonimmune rat IgE and anti-DNP mouse IgE, only the latter underwent redistribution. Vesicles containing DNP-lipids bound to RBL cells carrying anti-DNP IgE but not to cells carrying nonimmune rat IgE. Measurable nonspecific binding did not develop even after 15 min of pushing DNP-bearing vesicles against RBL cells sensitized with nonimmune IgE. Neither redistribution nor adhesion was blocked by metabolic poisons such as NaN3 and NaF. Both redistribution and adhesion occurred in plasma membrane blebs previously shown to lack cytoskeletal filaments. The above observations are consistent with contact-induced redistribution of the IgE being a result of passive diffusion-mediated trapping rather than active cellular responses. Thus, long-range diffusion of specific proteins can in some cases contribute to the formation of stable adhesion between membranes.Keywords
This publication has 28 references indexed in Scilit:
- Availability of dinitrophenylated lipid haptens for specific antibody binding depends on the physical properties of host bilayer membranes.Journal of Biological Chemistry, 1982
- Rapid lateral diffusion of functional ACh receptors in embryonic muscle cell membraneNature, 1982
- Enhanced molecular diffusibility in muscle membrane blebs: release of lateral constraints.The Journal of cell biology, 1982
- Localization of cell membrane components by surface diffusion into a "trap"Biophysical Journal, 1981
- Formation of ACh receptor clusters induced by positively charged latex beadsNature, 1981
- Affinity of red blood cell membrane for particle surfaces measured by the extent of particle encapsulationBiophysical Journal, 1981
- IgE‐induced histamine release from rat basophilic leukemia cell lines: isolation of releasing and nonreleasing clonesEuropean Journal of Immunology, 1981
- Kinetics of antibody-dependent binding of haptenated phospholipid vesicles to a macrophage-related cell lineBiochemistry, 1980
- Monoclonal dinitrophenyl-specific murine IgE antibody: preparation, isolation, and characterization.The Journal of Immunology, 1980
- Minimum energy analysis of membrane deformation applied to pipet aspiration and surface adhesion of red blood cellsBiophysical Journal, 1980