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Title: Studies involving the induction of prostaglandin synthesis following cell transformation by herpes simplex virus type 2

Thesis/Dissertation ·
OSTI ID:6291842

The purpose of this study was to determine the effect of HSV-2 transformation on cellular metabolic processes, specifically the metabolism of arachidonic acid (20:4) and prostaglandin (PG) synthesis. Results obtained by labeling cells with (/sup 3/H)20:4 and analyzing the release of radioactivity into overlay culture medium demonstrate that while nontransformed rat embryo fibroblasts (REF) possess phospholipase to catalyze the release of 20:4 from membrane phospholipids, transformation of REF cells by photoinactivated HSV-2 virions induces cyclooxygenase to convert 20:4 substrate primarily to PGE/sub 2/ and PGF/sub 2..cap alpha../. Induction of 20:4 deacylation in nontransformed and HSV-2 transformed cells as well as PG synthesis in transformed cells is further enhanced by the tumor promoter (12-O-tetradecanoylphorbol-13-acetate (TPA) and calcium ionophore A23187. Phospholipase and cyclooxygenase appear to be coupled in their regulation in HSV-2 transformed tumor-derived rat fibrosarcoma (RFS) cells. Three times more (/sup 3/H)20:4 is incorporated into the phosphatidylserine/phosphatidylinositol (PS/PI) fraction in HSV-2 transformed cells compared to REF cells; additionally, this fraction serves as the primary donor of (/sup 3/H)20:4 released from TPA-stimulated transformed cells.

Research Organization:
Wake Forest Univ., Winston-Salem, NC (USA)
OSTI ID:
6291842
Resource Relation:
Other Information: Thesis (Ph. D.)
Country of Publication:
United States
Language:
English