| Literature DB >> 3478039 |
Abstract
These processes depend upon the catabolism of glucose, which can be inhibited by fluoride (F-). We studied them with a radiolabelling technique using [3H]-uridine, which is incorporated into viable yeast cells, but hardly at all into neutrophils and dead or phagocytosed yeast cells. Lysis of neutrophils and treatment of the lysate with [3H]-uridine allowed estimation of intracellular killing of yeast cells. F- inhibited neutrophil phagocytosis and intracellular killing in a dose-related manner. Intracellular killing was significantly more sensitive to environmental F- than was phagocytosis. This effect on phagocytosis was not because of inhibition of opsonization of yeast, nor was it related to an effect on medium Ca2+.Entities:
Mesh:
Substances:
Year: 1987 PMID: 3478039 DOI: 10.1016/0003-9969(87)90092-6
Source DB: PubMed Journal: Arch Oral Biol ISSN: 0003-9969 Impact factor: 2.633