The DNA-damaging ability of benzene and its metabolites on peripheral blood mononuclear cells (PBMC) has been investigated by using the alkaline comet assay. The PBMC were incubated with different compounds in two different media for 2 and 24 hr at concentrations that did not affect cell viability a
Effect of serum on prostaglandin production during the co-culture of human thyroid cells and peripheral blood mononuclear cells
β Scribed by E. A. Herman; M. Yamamoto; Dr. B. Rapoport
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 439 KB
- Volume
- 100
- Category
- Article
- ISSN
- 0021-9541
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Prostaglandin generation by human peripheral blood mononuclear cells is enhanced during coβculture with human thyroid cells. The objective of the present study was to determine the influence of various sera on this process.
Human thyroid adenoma cell monolayers were cultured with normal human peripheral blood mononuclear cells for three days in the presence of a variety of sera, or serum fractions. Prostaglandin E (PGE) in the medium was measured by bioassay or by radioimmunoassay. Significantly more PGE was generated in cultures containing fetal calf serum than in those containing human serum. This difference was not abolished by dialysis of the human serum. When the 50% (NH~4~) ~2~SO~4~ precipitate of the serum was used, PGE generation was similar to that in fetal calf serum, indicating the presence of an inhibitory factor in human serum. The degree of this inhibitory activity was similar in autologous and heterologous human serum, as well as in normal subjects and patients with Graves' disease. Gel filtration and ionβexchange chomatography of human serum showed the inhibitor to coβmigrate with albumin. Evidence presented suggests that the inhibitor is not albumin itself but is, instead, a factor tightly bound to albumin. Inhibitory activity was also found in rabbit, goat, rat and cow serum.
Prostaglandins are potent modulators of immuneβcell function. These data indicate that this process may be modulated by a factor in mammalian serum. The relative absence of this factor in fetal serum may have important implications in regard to the profound changes which occur in the immune system after birth.
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