Figure 3
Figure 3. Comparative phenotypic characterization of clathrin pits and caveolae in uninfected reticulocytes and P vivax IRBCs. (A) Representative AFM scans that illustrate the presence and density of clathrin pits on uninfected reticulocytes and of caveolae on P vivax IRBCs; the bottom inserts show the shape of these 2 nanostructures as revealed by transmission electron microscopy. (B) The range of the diameters of the 2 nanostructures observed on uninfected reticulocytes and on P vivax IRBCs and (C) changes in the distribution of caveolae and clathrin pits with the ex vivo maturation of the P vivax IRBCs (both observations derived from the same 13 independent isolates [staged ex vivo maturation], with total of 485 IRBCs examined). The P vivax isolates we received for this staged ex vivo maturation were >6 hours old (n = 10), thus we needed to conduct 3 invasion assays (n = 3) to get AFM data on the missing 0 to 6 hour postinvasion window (tiny ring stage). (D) Representative AFM scans of P vivax IRBCs at various stages of development and the directly corresponding Giemsa-stained picture. This set of scans was taken from staged ex vivo invasion and maturation assay. Bar represents 10 μm.

Comparative phenotypic characterization of clathrin pits and caveolae in uninfected reticulocytes and P vivax IRBCs. (A) Representative AFM scans that illustrate the presence and density of clathrin pits on uninfected reticulocytes and of caveolae on P vivax IRBCs; the bottom inserts show the shape of these 2 nanostructures as revealed by transmission electron microscopy. (B) The range of the diameters of the 2 nanostructures observed on uninfected reticulocytes and on P vivax IRBCs and (C) changes in the distribution of caveolae and clathrin pits with the ex vivo maturation of the P vivax IRBCs (both observations derived from the same 13 independent isolates [staged ex vivo maturation], with total of 485 IRBCs examined). The P vivax isolates we received for this staged ex vivo maturation were >6 hours old (n = 10), thus we needed to conduct 3 invasion assays (n = 3) to get AFM data on the missing 0 to 6 hour postinvasion window (tiny ring stage). (D) Representative AFM scans of P vivax IRBCs at various stages of development and the directly corresponding Giemsa-stained picture. This set of scans was taken from staged ex vivo invasion and maturation assay. Bar represents 10 μm.

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