Table 3.

Mast Cell Development From Bone Marrow Cells in a Liquid Culture

StimulantMast Cells/Culture3-150 (104 ± SD)Histamine/Culture (μg ± SD)Endogenous
(10 ng/mL)IL-3 in Supernatants3-151
None Undetectable 
PGE Undetectable 
rIFN-γ Undetectable 
rTNF-α Undetectable 
rIL-6 Undetectable 
rIL-3 40.8 ± 3.8 0.2051 ± 0.0034 
rIL-3 + PGE 163.3 ± 10.2 0.4059 ± 0.03133-152 
rIL-3 + rINF-γ 100.4 ± 16.2 0.5185 ± 0.04013-152 
rIL-3 + rTNF-α 73.3 ± 9.2 0.2317 ± 0.01353-152 
rIL-3 ± rIL-6 146.2 ± 51.1 0.5106 ± 0.04723-152 
StimulantMast Cells/Culture3-150 (104 ± SD)Histamine/Culture (μg ± SD)Endogenous
(10 ng/mL)IL-3 in Supernatants3-151
None Undetectable 
PGE Undetectable 
rIFN-γ Undetectable 
rTNF-α Undetectable 
rIL-6 Undetectable 
rIL-3 40.8 ± 3.8 0.2051 ± 0.0034 
rIL-3 + PGE 163.3 ± 10.2 0.4059 ± 0.03133-152 
rIL-3 + rINF-γ 100.4 ± 16.2 0.5185 ± 0.04013-152 
rIL-3 + rTNF-α 73.3 ± 9.2 0.2317 ± 0.01353-152 
rIL-3 ± rIL-6 146.2 ± 51.1 0.5106 ± 0.04723-152 
F3-150

Mouse bone marrow cells were cultured with complete culture medium. Various cytokines were added at the start of the cultures. Considering the lack of endogenous IL-3 and the property of IL-3–dependent manner of MMC, rIL-3 was replenished at each feeding. Mast cell number and histamine quantity per culture were determined on day 12.

F3-151

Endogenous IL-3 in the supernatants recovered from the cultures on days 2 and 4 was detected by ELISA.

F3-152

P < .01 compared with data of rIL-3 alone.

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