Morisaki N, Lindsey J A, Milo G E, Cornwell D G
Lipids. 1983 May;18(5):349-52. doi: 10.1007/BF02537230.
Primary cultures of smooth muscle cells were established from the medial layer of guinea pig aorta. Cells were seeded at from 40 to 80 cells per cm2 and cloned for 8 days. Media were analyzed for PGI2 (6-keto-PGF1 alpha) using radioimmunoassay. Prostanoids were synthesized when cells were grown in media alone. Arachidonic acid stimulated prostanoid synthesis and promoted cell proliferation. Indomethacin blocked prostanoid synthesis and abolished the stimulatory effect of arachidonic acid on cell proliferation. Hydralazine stimulated fatty acid release and prostanoid synthesis in confluent cells. Hydralazine also stimulated prostanoid synthesis and promoted proliferation in growing cells. Indomethacin blocked prostanoid synthesis and abolished the stimulatory effect of hydralazine on cell proliferation.
平滑肌细胞的原代培养物取自豚鼠主动脉中层。细胞以每平方厘米40至80个细胞的密度接种,并克隆培养8天。使用放射免疫分析法分析培养基中的前列环素(6-酮-前列腺素F1α)。当细胞单独在培养基中生长时会合成前列腺素。花生四烯酸刺激前列腺素合成并促进细胞增殖。吲哚美辛阻断前列腺素合成并消除花生四烯酸对细胞增殖的刺激作用。肼屈嗪刺激融合细胞中的脂肪酸释放和前列腺素合成。肼屈嗪还刺激生长中的细胞合成前列腺素并促进其增殖。吲哚美辛阻断前列腺素合成并消除肼屈嗪对细胞增殖的刺激作用。