Phosphatidylethanolamine synthesis in ethanolamine‐responsive and ‐nonresponsive cells in culture

Abstract

Mammalian cells can be classified into two types based upon whether or not they show growth response to ethanolamine (Etn) in culture. The content of phosphatidylethanolamine (PE) in phospholipid and incorporation of radioactive Etn into the cells were examined in the Etn‐responsive and ‐nonrespponsive cells in order to elucidate the mechanisms of growth stimulation by Etn. In all Etn‐responsive cells tested, 5 μM Etn significantly altered the composition of cellular phospholipid compared to that grown without Etn, while Etn‐nonresponsive cells had a similar phospholipid composition whether the growth medium contained Etn or not. Using two rat mammary carcinoma cell lines, 64–24 (responsive type) and 22‐1 (nonresponsive type), further studies were carried out. In 64–24 cells there was a proportional increase in PE content as the dosage of Etn in the medium was increased. The increase in PE content leveled off at 10 μM. Further, the increase in PE content was correlated with increased rate of growth. In contrast, PE content or growth rate did not change at all in 22‐1 cells. In 64–24 cells radioactive Etn (0.1–50 μM) was incorporated four‐ to five‐fold more efficiently into phospholipid, and the aqueous pool of precursors of PE was ten times less as compared to 22‐1 cells, indicating that Etn‐responsive cells utilize Etn supplied in the medium to synthesize PE far more efficiently than Etn‐nonresponsive cells. De novo synthesis of PE must not be sufficient to support optimum growth in Etn‐responsive cells.