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Resolution: standard / high Figure 1.
Schematic visualization of endocytic routes adopted by various GPI-Anchored proteins
and other endocytic markers. A) Various membrane resident proteins and lipids like FR-GPI, prions, LRP, uPAR,
cholesterol, sphingolipids and cholera-toxin bound to GM1 are present in a diffuse
distribution in the plasma membrane. B) GPI-APs like FR-GPI align with cholesterol
and sphingolipids to form lateral aggregates termed as rafts. uPAR and prion proteins,
although GPI-anchored, interact with LRP and are endocytosed into the clathrin-coated
pits. The interaction of the protein domains of uPAR and Prion with LRP seems to override
the influence of the lateral segregation into rafts mediated by the GPI-anchor of
these proteins. LRP has signal sequences in the cytoplasmic domain for recruitment
into clathrin-coated pits. C and D) Raft-included markers like FR-GPI and cholera
toxin bound to GM1 are endocytosed into GEECs whereas uPAR:LRP and prion;LRP complexes
are endocytosed into vacuoles derived from clathrin-coated pits.
Lakhan et al. Journal of Biomedical Science 2009 16:93 doi:10.1186/1423-0127-16-93 |