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Lateral diffusion anisotropy and membrane lipid/skeleton interaction in outer hair cells.
J Boutet de Monvel1, W E Brownell, M Ulfendahl
1Center for Hearing and Communication Research, Karolinska Institutet, Stockholm, Sweden. j.boutet.de.monvel@ki.se
Biophysical Journal
|April 11, 2006
Summary
Cell membrane fluidity in cochlear outer hair cells (OHCs) exhibits directional lipid diffusion, influenced by the cell
Area of Science:
- Cell Biology
- Biophysics
- Auditory Science
Background:
- The plasma membrane's lipid organization into domains influences its interaction with the underlying protein skeleton, affecting molecular mobility.
- Membrane fluidity is crucial for cellular functions and can be assessed using techniques like fluorescence recovery after photobleaching (FRAP).
Purpose of the Study:
- To analyze the two-dimensional pattern of lipid diffusion in the lateral plasma membrane of cochlear outer hair cells (OHCs).
- To investigate the influence of turgor pressure and the membrane skeleton on OHC membrane lipid mobility.
Main Methods:
- Utilized fluorescence recovery after photobleaching (FRAP) to measure lipid diffusion in isolated OHCs and intact temporal bone preparations.
- Analyzed the two-dimensional diffusion patterns of lipids in the OHC lateral membrane.
- Performed osmotic challenges to alter cell turgor pressure and observed effects on lipid diffusion.
Main Results:
- Membrane lipid mobility in OHCs is orthotropic, with faster diffusion along the cell's axial direction and slower diffusion circumferentially.
- Increased turgor pressure reduced axial diffusion but had minimal impact on circumferential diffusion.
- Lipid mobility in OHCs and inner hair cells within the intact organ was comparable, suggesting similar fluid membrane phases; supporting cells showed slower mobility.
Conclusions:
- The OHC plasma membrane skeleton, potentially spectrin filaments, influences lipid mobility, leading to orthotropic diffusion.
- The findings support the notion of similar, highly fluid membrane phases in both OHCs and inner hair cells within the intact cochlea.
- Differences in lipid mobility between hair cells and supporting cells may indicate distinct lipid compositions or cytoskeletal interactions.