Figure 1.
Figure 1. Presence of raft markers in reticulocyte exosomes. (A) Equivalent protein amounts of ghosts, exosomes, and LDTI membranes from rat reticulocytes (exceeding 70%) were loaded on 10% SDS-PAGE and analyzed by Western blotting for Lyn and the TfR. (B) Because of GARP-50 antibody specificity, human red cells (6% reticulocytes) were subcultured in vitro. Red cell ghosts and exosomes collected from the medium were analyzed by Western blotting for human stomatin (GARP-50) and then for flotillin. (C) Rat reticulocytes (40 μL packed cell volume) were incubated with (50 μg/mL) biotinylated B-subunit of cholera toxin (bCTXB) for 3 hours at 4°C and chased for 60 minutes at 37°C. Cells were then fixed in 2% paraformaldehyde and processed as described in “Materials and methods.”

Presence of raft markers in reticulocyte exosomes. (A) Equivalent protein amounts of ghosts, exosomes, and LDTI membranes from rat reticulocytes (exceeding 70%) were loaded on 10% SDS-PAGE and analyzed by Western blotting for Lyn and the TfR. (B) Because of GARP-50 antibody specificity, human red cells (6% reticulocytes) were subcultured in vitro. Red cell ghosts and exosomes collected from the medium were analyzed by Western blotting for human stomatin (GARP-50) and then for flotillin. (C) Rat reticulocytes (40 μL packed cell volume) were incubated with (50 μg/mL) biotinylated B-subunit of cholera toxin (bCTXB) for 3 hours at 4°C and chased for 60 minutes at 37°C. Cells were then fixed in 2% paraformaldehyde and processed as described in “Materials and methods.”

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