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The uptake of amines by polymorphonuclear leukocytes
Biochimica Et Biophysica Acta
|May 6, 1981
Summary
Ligands bind to immune cells, but this process differs from receptor binding. Permeable basic amines accumulate in cell lysosomes, indicating a distinct cellular mechanism.
Area of Science:
- Pharmacology
- Cell Biology
- Immunology
Background:
- Muscarinic and beta-adrenergic ligands bind to polymorphonuclear leukocytes.
- This association exhibits characteristics of high-affinity, saturable accumulation.
Purpose of the Study:
- To differentiate ligand association from specific receptor binding in polymorphonuclear leukocytes.
- To investigate the mechanism of permeable basic amine accumulation in these cells.
Main Methods:
- Characterizing ligand association based on temperature dependence, pH sensitivity, energy requirements, and inhibition by ionophores and permeable basic amines.
- Analyzing the effect of permeable basic amines on specific receptor binding.
Main Results:
- Ligand association differs from specific receptor binding due to its temperature dependence, pH sensitivity, energy requirement, and inhibition by ionophores.
- Permeable basic amines accumulate in acidic lysosomes within polymorphonuclear leukocytes.
- This amine accumulation can be inhibited independently of specific receptor binding.
Conclusions:
- The observed ligand association is distinct from specific receptor binding and likely involves lysosomal accumulation.
- Permeable basic amines accumulate in acidic lysosomes, providing a method to distinguish this process from direct receptor interactions.