Muir J G, Murray A W
Biochim Biophys Acta. 1986 Feb 21;885(2):176-84. doi: 10.1016/0167-4889(86)90086-8.
The biosynthesis of phosphatidylcholine (PC) in HEL-37 cells was followed by measuring the incorporation of [32P]Pi into PC. Incorporation was stimulated by 12-O-tetradecanoylphorbol 13-acetate (TPA) and by the synthetic diacylglycerol, sn-1,2-dioctanoylglycerol (diC8), but not by sn-1-oleoyl-2-acetylglycerol or sn-1,2-dihexanoylglycerol (diC6). DiC8 was rapidly metabolised by HEL-37 cells to the corresponding PC and phosphatidic acid derivatives. diC8, diC6 and oleoylacetylglycerol effectively displaced [3H]phorbol-12,13-dibutyrate bound to a soluble cell extract from HEL-37 cells, but only diC8 was able to displace the labelled phorbol ester from prelabelled cells. TPA, diC8, diC6 and oleoylacetylglycerol were all effective inhibitors of 125I-labelled epidermal growth factor binding to, and gap junctional communication between, HEL-37 cells. It is concluded that only cell-permeable diacylglycerols stimulate PC biosynthesis which may therefore require interaction with membranes other than the plasma membrane.
通过测量[32P]Pi掺入磷脂酰胆碱(PC)的情况来追踪HEL - 37细胞中PC的生物合成。掺入受到12 - O - 十四酰佛波醇13 - 乙酸酯(TPA)和合成二酰基甘油sn - 1,2 - 二辛酰甘油(diC8)的刺激,但不受sn - 1 - 油酰基 - 2 - 乙酰甘油或sn - 1,2 - 二己酰甘油(diC6)的刺激。DiC8被HEL - 37细胞迅速代谢为相应的PC和磷脂酸衍生物。diC8、diC6和油酰乙酰甘油能有效取代与HEL - 37细胞可溶性细胞提取物结合的[3H]佛波醇 - 12,13 - 二丁酸酯,但只有diC8能够从预先标记的细胞中取代标记的佛波醇酯。TPA、diC8、diC6和油酰乙酰甘油都是125I标记的表皮生长因子与HEL - 37细胞结合以及细胞间缝隙连接通讯的有效抑制剂。得出的结论是,只有可穿透细胞的二酰基甘油能刺激PC生物合成,因此这可能需要与质膜以外的其他膜相互作用。