Honma Y, Kasukabe T, Hozumi M, Koshihara Y
J Cell Physiol. 1980 Sep;104(3):349-57. doi: 10.1002/jcp.1041040308.
Mouse myeloid leukemia cells (Ml) were induced to differentiate into mature macrophages and granulocytes by various inducers. The differentiated Ml cells synthesized and released prosetaglandins, whereas untreated Ml cells did not. When the cells wee prelabelled with [14C]arachidonate, the major prostaglandins released into the culture media were found to be prostaglandin E2, D2, and F2 alpha in an early stage of differentiation, but the mature cells produced predominantly prostaglandin E2. The synthesis and release of prostaglandins were completely inhibited by indomethacin. Dexamethasone, a potent inducer of differentiation of Ml cells, did not induce production of prostaglandins in resistant Ml cells that could not differentiate even with a high concentration of dexamethasone. These results suggest that production of prostaglandins in Ml cells is closely associated with differentiation of the cells. Homogenates of dexamethasone-treated Ml cells converted arachidonate to prostaglandins, but this conversion was scarcely observed with homogenates of untreated Ml cells. Dexamethasone and the other inducers stimulated the release of arachidonate from phospholipids. Therefore, induction of prostaglandin synthesis during differentiation of Ml cells may result from induction of prostaglandin synthetase activity and stimulation of the release of arachidonate from cellular lipids. Lysozyme activity, which is a typical biochemical marker of macrophages, was induced in Ml cells by prostaglandin E2 or D2 alone, as well as by inducers of differentiation of the cells, but it was not induced by arachidonate or prostaglandin F2 alpha. These results suggest that prostaglandin synthesis is important in differentiation of myeloid leukemia cells.
小鼠髓性白血病细胞(Ml)可通过各种诱导剂诱导分化为成熟的巨噬细胞和粒细胞。分化后的Ml细胞合成并释放前列腺素,而未处理的Ml细胞则不会。当细胞用[14C]花生四烯酸预标记时,发现在分化早期释放到培养基中的主要前列腺素是前列腺素E2、D2和F2α,但成熟细胞主要产生前列腺素E2。吲哚美辛可完全抑制前列腺素的合成和释放。地塞米松是Ml细胞分化的有效诱导剂,但在即使使用高浓度地塞米松也无法分化的抗性Ml细胞中,它不会诱导前列腺素的产生。这些结果表明,Ml细胞中前列腺素的产生与细胞的分化密切相关。用地塞米松处理的Ml细胞匀浆可将花生四烯酸转化为前列腺素,但未处理的Ml细胞匀浆几乎未观察到这种转化。地塞米松和其他诱导剂刺激了花生四烯酸从磷脂中的释放。因此,Ml细胞分化过程中前列腺素合成的诱导可能是由于前列腺素合成酶活性的诱导以及细胞脂质中花生四烯酸释放的刺激。溶菌酶活性是巨噬细胞的一种典型生化标志物,仅前列腺素E2或D2以及细胞分化诱导剂可在Ml细胞中诱导其产生,但花生四烯酸或前列腺素F2α不会诱导其产生。这些结果表明,前列腺素合成在髓性白血病细胞的分化中很重要。