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Protamine reversibly decreases paracellular cation permeability in Necturus gallbladder.
The Journal of Membrane Biology
|January 1, 1985
Summary
Protamine, a protein, reversibly reduces cation permeability across the Necturus gallbladder tight junction. This protein affects ion transport and water movement, with effects reversed by heparin.
Area of Science:
- Physiology
- Cell Biology
- Biochemistry
Background:
- Tight junctions regulate paracellular permeability in epithelial tissues.
- Polycationic proteins like protamine can interact with cell membranes and influence ion transport.
Purpose of the Study:
- To investigate the effect of protamine on the electrical resistance and ion permeability of the Necturus gallbladder epithelium.
- To elucidate the mechanism by which protamine alters tight junction function.
Main Methods:
- Transepithelial AC-impedance technique was used to measure electrical resistance in Necturus gallbladder.
- Protamine sulfate/hydrochloride was applied to the mucosal bath, and effects on resistance, voltage, and ion conductance were monitored.
- Reversal of protamine's effects was tested using mucosal heparin and serosal ouabain.
Main Results:
- Protamine significantly increased transepithelial resistance by 89% and altered transepithelial voltage.
- The effects were concentration-dependent, with maximal response at 10-20 microM.
- Protamine reversibly decreased K+ and Na+ conductance by a factor of 3 but not Cl- conductance.
- Net water transport increased by 60% with protamine, and effects were reversible by heparin.
Conclusions:
- Protamine reversibly decreases the conductance of the cation-selective pathway through the tight junction.
- Protamine may exert its effect by binding to the apical membrane, inducing intracellular events that alter tight junction structure.
- This suggests a novel mechanism for regulating paracellular permeability by polycationic proteins.