Fig. 1.
Fig. 1. Collagen-mediated changes in [Ca2+]i in megakaryocytes from wild-type and syk −/− mice. Megakaryocytes from either (A) wild-type Balb/c mice or (B) radiation chimeric Balb/c mice repopulated with syk −/− fetal liver were isolated from bone marrow as described. After plating onto poly-L-lysine–coated coverslips, stage III/IV megakaryocytes were identified and injected with FURA-2 and then stimulated with collagen (100 μg/mL) as indicated. [Ca2+]e levels were adjusted 2 minutes before the addition of agonist. FURA-2 fluorescence was measured as described and [Ca2+]i was determined from a precalculated calibration curve. Representative traces in (A) and (B) are each taken from cells from a single animal, but a representative of at least 6 (A) or 3 (B) cells from a minimum of three mice.

Collagen-mediated changes in [Ca2+]i in megakaryocytes from wild-type and syk −/− mice. Megakaryocytes from either (A) wild-type Balb/c mice or (B) radiation chimeric Balb/c mice repopulated with syk −/− fetal liver were isolated from bone marrow as described. After plating onto poly-L-lysine–coated coverslips, stage III/IV megakaryocytes were identified and injected with FURA-2 and then stimulated with collagen (100 μg/mL) as indicated. [Ca2+]e levels were adjusted 2 minutes before the addition of agonist. FURA-2 fluorescence was measured as described and [Ca2+]i was determined from a precalculated calibration curve. Representative traces in (A) and (B) are each taken from cells from a single animal, but a representative of at least 6 (A) or 3 (B) cells from a minimum of three mice.

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