Leukotriene C4 metabolism by hepatoma cells deficient in the uptake of cysteinyl leukotrienes

• Published in: European journal of biochemistry Vol. 154; no. 3; pp. 559 - 562
• Main Authors: WECKBECKER, Gisbert, KEPPLER, Dietrich O. R.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 03.02.1986; Blackwell
• Subjects: Animals; Applied sciences; Biological Transport; Cells, Cultured; Exact sciences and technology; Female; Liver - metabolism; Liver Neoplasms, Experimental - metabolism; Other techniques and industries; Rats; SRS-A - metabolism
• ISSN: 0014-2956; 1432-1033
• DOI: 10.1111/j.1432-1033.1986.tb09435.x

Uptake and metabolism of the cysteinyl leukotrienes C4 and E4 (LTC4 and LTE4) were studied in AS‐30D hepatoma cell suspensions and compared with rat hepatocytes. The hepatoma cells were deficient in the uptake of [3H]LTC4 and [3H]LTE4 but took up, in control experiments, l‐[14C]glutamine and [14C]adenosine in a time‐dependent manner. By contrast, isolated hepatocyte suspensions incubated under the same conditions took up [3H]LTC4 and [3H]LTE4 as well as l‐[14C]glutamine and [14C]adenosine. The hepatoma cells deficient in the uptake of cysteinyl leukotrienes metabolized extracellular [3H]LTC4 to [3H]LTD4 and to [3H]LTE4. Addition of acivicin, an inhibitor of γ‐glutamyltransferase, largely prevented metabolism of [3H]LTC4 by the hepatoma cells. Sonication of the cells did not enhance the formation of [3H]LTD4 and [3H]LTE4 from [3H]LTC4. We conclude that ectoenzymes of AS‐30D hepatoma cells catalyze the conversion of LTC4 to LTE4 via LTD4. As compared to hepatocytes, these neoplastic cells have lost the uptake system for cysteinyl leukotrienes and may serve in studies on leukotriene metabolism by cell‐surface enzymes.