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F-Met-Leu-Phe and echo 9 virus interaction with human granulocytes. Changes of cell membrane structure
Abstract:
Biophysical and biochemical methods were applied for investigation of cell membrane properties of human polymorphonuclear leukocytes (PMNs) exposed to the chemotactic peptide N-formylmethionyl-leucylphenylalanine (f-Met-Leu-Phe) and echovirus type 9, strain A, Barty. Steady-state fluorescence depolarization with diphenylhexatriene demonstrated no gross changes of the total membrane fluidity under the different experimental conditions. However, by means of the monomer-excimer technique with pyrenedecanoic acid (PDA), significant changes of the local membrane structure were detected for both agents. As demonstrated by a higher excimer ratio, the membrane area available for the PDA molecules was restricted by f-Met-Leu-Phe. This effect was dependent on the dose and on the time of interaction of the chemotactic peptide. These experimental findings were explained by the formation of functional receptor units ("activated membrane"). Echo 9 virus exhibited the opposite effect, characterized by a higher ratio of monomers, which also depended on the viral dose and the time of virus-PMN interaction. These virus-induced findings were explained by the dissolution of functional receptor units. Consecutive exposure of the PMNs to f-Met-Leu-Phe and echovirus, or vice versa, demonstrated a virus-predominant effect on the membrane structures.
Insights
Human polymorphonuclear leukocytes (PMNs) membrane fluidity remains unchanged by f-Met-Leu-Phe or echovirus. However, local membrane structure is altered, with f-Met-Leu-Phe restricting space and echovirus dissolving receptor units.
Area of Science:
- Biophysics
- Cell Biology
- Immunology
Background:
- Human polymorphonuclear leukocytes (PMNs) are crucial immune cells.
- Chemotactic peptides and viruses can alter PMN function and membrane properties.
Purpose of the Study:
- To investigate the effects of f-Met-Leu-Phe and echovirus 9 on PMN cell membrane properties.
- To understand the mechanisms of PMN activation and viral interaction at the membrane level.
Main Methods:
- Steady-state fluorescence depolarization using diphenylhexatriene.
- Monomer-excimer technique with pyrenedecanoic acid (PDA).
Main Results:
- No significant changes in overall membrane fluidity were observed.
- f-Met-Leu-Phe restricted the membrane area available for PDA, suggesting functional receptor unit formation.
- Echovirus 9 caused the opposite effect, indicating dissolution of functional receptor units.
- Virus-induced effects predominated in sequential exposures.
Conclusions:
- Chemotactic peptide and viral interactions induce distinct alterations in PMN local membrane structure.
- These changes are linked to the formation or dissolution of functional receptor units.
- Viral effects appear dominant over peptide effects in modulating PMN membrane structure.