Fig. 5.
Fig. 5. Effects of LTD4 on immature CD34+/CD38low/− hematopoietic progenitor cells. / (A) Isolated PB CD34+ progenitor cells were loaded with the calcium indicator Fluo-3 and stained with a CD38-PE antibody. Ten seconds after addition of LTD4, a shift of the green Fluo-3 fluorescence was observed due to intracellular calcium mobilization (right panel), which occurred in both CD38+ and more primitive CD38low/− progenitor cells. (B) Analysis of isolated PB CD34+ cells by flow cytometry before and after chemotaxis showed a similar percentage of more immature CD34+/CD38low/− cells (bold rectangular gate) in the starting population (ii, before migration, 5.25%), in spontaneously migrating cells (iii, 6.15%), and in migrated cells attracted by LTD4 (iv, 6.35%). In this particular experiment, a more than 2-fold increase of the migration rate in response to LTD4 (50 nM) was observed. The isotype-specific control is shown in panel i.

Effects of LTD4 on immature CD34+/CD38low/− hematopoietic progenitor cells.

(A) Isolated PB CD34+ progenitor cells were loaded with the calcium indicator Fluo-3 and stained with a CD38-PE antibody. Ten seconds after addition of LTD4, a shift of the green Fluo-3 fluorescence was observed due to intracellular calcium mobilization (right panel), which occurred in both CD38+ and more primitive CD38low/− progenitor cells. (B) Analysis of isolated PB CD34+ cells by flow cytometry before and after chemotaxis showed a similar percentage of more immature CD34+/CD38low/− cells (bold rectangular gate) in the starting population (ii, before migration, 5.25%), in spontaneously migrating cells (iii, 6.15%), and in migrated cells attracted by LTD4 (iv, 6.35%). In this particular experiment, a more than 2-fold increase of the migration rate in response to LTD4 (50 nM) was observed. The isotype-specific control is shown in panel i.

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