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Phase coexistence and connectivity in the apical membrane of polarized epithelial cells
Open accessAbstract
Although it is well described in model membranes, little is known about phase separation in biological membranes. Here, we provide evidence for a coexistence of at least two different lipid bilayer phases in the apical plasma membrane of epithelial cells. Phase connectivity was assessed by measuring long-range diffusion of several membrane proteins by fluorescence recovery after photobleaching in two polarized epithelial cell lines and one fibroblast cell line. In contrast to the fibroblast plasma membrane, in which all of the proteins diffused with similar characteristics, in the apical membrane of epithelial cells the proteins could be divided into two groups according to their diffusion characteristics. At room temperature (≈25°C), one group showed fast diffusion and complete recovery. The other diffused three to four times slower and, more importantly, displayed only partial recovery. Only the first group comprises proteins that are believed to be associated with lipid rafts. The partial recovery is not caused by topological constraints (microvilli, etc.), cytoskeletal constraints, or protein-protein interactions, because all proteins show 100% recovery in fluorescence recovery after photobleaching experiments at 37°C. In addition, the raft-associated proteins cannot be coclustered by antibodies on the apical membrane at 12°C. The interpretation that best fits these data is that the apical membrane of epithelial cells is a phase-separated system with a continuous (percolating) raft phase <25°C in which isolated domains of the nonraft phase are dispersed, whereas at 37°C the nonraft phase becomes the continuous phase with isolated domains of the raft phase dispersed in it.
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Citations
Cited by
Membrane lipids: where they are and how they behave
van Meer, G., Voelker, D. R., & Feigenson, G. W. (2008) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2330 · Cited by 7,157
Lipid rafts as a membrane-organizing principle
Lingwood, D., & Simons, K. (2010) · Science · doi:10.1126/science.1174621 · Cited by 4,417
Self-citationRevitalizing membrane rafts: new tools and insights
Simons, K., & Gerl, M. J. (2010) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2977 · Cited by 1,234
Self-citationLarge-scale fluid/fluid phase separation of proteins and lipids in giant plasma membrane vesicles
Baumgart, T., Hammond, A. T., Sengupta, P., Hess, S. T., Holowka, D. A., Baird, B. A., & Webb, W. W. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0611357104 · Cited by 800
Dynamic molecular confinement in the plasma membrane by microdomains and the cytoskeleton meshwork
Lenne, P., Wawrezinieck, L., Conchonaud, F., Wurtz, O., Boned, A., Guo, X., Rigneault, H., He, H., & Marguet, D. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7601214 · Cited by 484
Metadata
- Authors
- Meder, D., Moreno, M. J., Verkade, P., Vaz, W. L. C., & Simons, K.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2006-01-03
- Volume
- 103
- Issue
- 2
- Pages
- 329-334
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2164227168
- Cited by
- 163
- References
- 0
- FWCI
- 7.12
- Type
- journal article
- Language
- en
- Open access
- green
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- Meder, D., Moreno, M. J., Verkade, P., Vaz, W. L. C., & Simons, K. (2006). Phase coexistence and connectivity in the apical membrane of polarized epithelial cells. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.0509885103
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