Warden L A, Menaldino D S, Wilson T, Liotta D C, Smith E R, Merrill A H
Department of Biochemistry, Emory University, Atlanta, Georgia 30322-3050, USA.
J Biol Chem. 1999 Nov 26;274(48):33875-80. doi: 10.1074/jbc.274.48.33875.
Cells in culture often undergo a "burst" of free sphingosine, sphingosine 1-phosphate, ceramide, and other bioactive lipids upon removal of "conditioned" medium, and at least one lipid signaling pathway (protein kinase C) has been shown to be affected by these changes (Smith, E. R. & Merrill A. H., Jr. (1995) J. Biol. Chem. 270, 18749-18758; Smith, E. R., Jones, P. L., Boss, J. M. & Merrill, A. H., Jr. (1997) J. Biol. Chem. 272, 5640-5646). Whereas increases in sphinganine and dihydroceramide are responses to provision of precursors for sphingolipid biosynthesis de novo in the new medium, the sphingosine burst is due to sphingolipid turnover upon removal of suppressive factor(s) in conditioned medium. This study describes the purification and characterization of these suppressive factors. Conditioned medium from J774 cells was fractionated into two components that suppress the burst as follows: ammonium ion, which reaches 2-3 mM within 48 h of cell culture; and a low molecular weight, cationic compound that has been assigned the structure 2, 6-bis(omega-aminobutyl)-3,5-diimino-piperazine (for which we suggest the name "batrachamine" based on its appearance) by (1)H and (13)C NMR, Fourier transform infrared spectroscopy, and mass spectrometric analyses. The physiological significance of these compounds as suppressors of sphingolipid metabolism is unclear; however, ammonium ion is a by-product of amino acid catabolism and reaches high concentrations in some tissues. Batrachamine is even more intriguing because this is, as far as we are aware, the first report of a naturally occurring compound of this structural type. Considering the many cell functions that are affected by sphingoid bases and their derivatives, the effects of NH(4) and batrachamine on sphingolipid metabolism may have important implications for cell regulation.
在去除“条件培养基”后,培养的细胞常常会经历游离鞘氨醇、鞘氨醇-1-磷酸、神经酰胺及其他生物活性脂质的“爆发”,并且至少有一条脂质信号通路(蛋白激酶C)已被证明会受这些变化的影响(史密斯,E.R. 及梅里尔,A.H., Jr.(1995年)《生物化学杂志》270, 18749 - 18758;史密斯,E.R., 琼斯,P.L., 博斯,J.M. 及梅里尔,A.H., Jr.(1997年)《生物化学杂志》272, 5640 - 5646)。鞘氨醇和二氢神经酰胺的增加是对新培养基中从头合成鞘脂的前体物质供应的反应,而鞘氨醇的爆发是由于去除条件培养基中的抑制因子后鞘脂的周转。本研究描述了这些抑制因子的纯化及特性。来自J774细胞的条件培养基被分离成两种抑制这种爆发的成分:铵离子,在细胞培养48小时内其浓度达到2 - 3 mM;以及一种低分子量的阳离子化合物,通过氢核磁共振、碳-13核磁共振、傅里叶变换红外光谱及质谱分析,其结构被确定为2, 6 - 双(ω-氨基丁基)- 3,5 - 二亚氨基哌嗪(基于其外观我们建议将其命名为“蟾胺”)。这些化合物作为鞘脂代谢抑制剂的生理意义尚不清楚;然而,铵离子是氨基酸分解代谢的副产物,在一些组织中会达到高浓度。蟾胺更具吸引力,因为据我们所知,这是关于这种结构类型的天然存在化合物的首次报道。考虑到鞘氨醇碱基及其衍生物会影响许多细胞功能,铵离子和蟾胺对鞘脂代谢的影响可能对细胞调节具有重要意义。