Thomas J M, Hullin F, Chap H, Douste-Blazy L
FEBS Lett. 1984 Oct 15;176(1):202-6. doi: 10.1016/0014-5793(84)80941-2.
Cultured endothelial cells (EC) from human umbilical vein were incubated with [U-14C]arachidonic acid (AA) followed by a challenge with thrombin (2 units/ml) or calcium ionophore A23187 (5 microM) for 0.5-10 min at 37 degrees C. In both cases, AA was rapidly liberated from phospholipids and converted into prostaglandin I2 (PGI2), as determined by the radioactivity of the stable derivative 6-keto-PGF1 alpha. Maximal liberation of AA and synthesis of PGI2 were achieved within 2 min, but the two compounds first accumulated in EC prior to their release into supernatants. This finding, which was never reported before, raises the question of the mechanism of AA and PG release through the cell membranes and offers a convenient model to investigate this still obscure process.
将人脐静脉培养的内皮细胞(EC)与[U-14C]花生四烯酸(AA)一起孵育,随后在37℃下用凝血酶(2单位/毫升)或钙离子载体A23187(5微摩尔)刺激0.5 - 10分钟。在这两种情况下,通过稳定衍生物6 - 酮 - PGF1α的放射性测定,AA迅速从磷脂中释放出来并转化为前列腺素I2(PGI2)。AA的最大释放量和PGI2的合成在2分钟内达到,但这两种化合物在释放到上清液之前首先在EC中积累。这一此前从未报道过的发现,引发了关于AA和PG通过细胞膜释放机制的问题,并提供了一个方便的模型来研究这个仍不清楚的过程。