mGal-1 induces proximal signaling events in leukocytes but fails to
induce PS exposure. A, HL60 cells treated with PBS for 4 h were
stained with annexin-V fluorescein isothiocyanate and propidium iodide
(PI) to detect PS exposure followed by flow cytometric analysis.
B, cells were loaded with Fluo-4 and analyzed for changes in
intracellular Ca2+ using a fluorometer following addition of PBS at
the indicated time (vertical arrow). C–F, HL60 cells
were loaded with Fluo-4 as in B, followed by addition of: 10
μm Gal-1 (C), 10 μm mGal-1 (D),
20 μm Gal-1 (E), or 20 μm mGal-1
(F) as indicated by the arrows. G-J, HL60 cells
treated with 10 μm Gal-1 (G), 10 μm
mGal-1 (H), 20 μm Gal-1 (I), or 20
μm mGal-1 (J) for 4 h were used to label cells with
annexin-V fluorescein isothiocyanate and PI to detect PS exposure followed by
flow cytometric analysis. K, HL60 cells were treated with the
indicated concentrations of Gal-1 or mGal-1 for 4 h followed by detection for
PS exposure.