Fig. 7.
Fig. 7. IL-1β and TNF-α production by CD34+ cells is not primarily responsible for increased IL-6 synthesis by HOB cells. Bone marrow CD34+ cells (0 to 1.0 × 104) were seeded directly onto confluent human osteoblast monolayers (HOB) in 96-well tissue culture plates containing 1% FBS. For these experiments, daily addition of murine neutralizing monoclonal IgG1 antibodies to human IL-1β, TNF-α, isotype-matched control, or vehicle were added at concentrations approaching 10 times the anticipated neutralizing dose (ND50 ) reported by the manufacturer (10 μg/mL). At 96 hours, conditioned medium was collected and assayed for IL-6 by ELISA. Data from a representative of two experiments are presented as the mean ± standard deviation for triplicate determinations.

IL-1β and TNF-α production by CD34+ cells is not primarily responsible for increased IL-6 synthesis by HOB cells. Bone marrow CD34+ cells (0 to 1.0 × 104) were seeded directly onto confluent human osteoblast monolayers (HOB) in 96-well tissue culture plates containing 1% FBS. For these experiments, daily addition of murine neutralizing monoclonal IgG1 antibodies to human IL-1β, TNF-α, isotype-matched control, or vehicle were added at concentrations approaching 10 times the anticipated neutralizing dose (ND50 ) reported by the manufacturer (10 μg/mL). At 96 hours, conditioned medium was collected and assayed for IL-6 by ELISA. Data from a representative of two experiments are presented as the mean ± standard deviation for triplicate determinations.

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