Gomez-Muñoz A, Hamza E H, Brindley D N
Department of Biochemistry, University of Alberta, Edmonton, Canada.
Biochim Biophys Acta. 1992 Jul 9;1127(1):49-56. doi: 10.1016/0005-2760(92)90200-f.
The activities of two phosphatidate phosphohydrolases were measured in cultured rat hepatocytes incubated with 0.1 mM albumin. The activity, which is inhibited by N-ethylmaleimide (PAP-1) is located in the cytosolic and membrane fractions. PAP-1 activity is stimulated by Mg2+ and it can be translocated from the cytosol to the membranes by relatively low (0.5-1 mM) concentrations of fatty acids. In addition, higher concentrations (1-3 mM) of fatty acids cause an increase in the total PAP-1 activity. Translocation of PAP-1 activity in the hepatocytes is preferentially promoted by unsaturated fatty acids (C18:1, C18:2, C18:3, C20:4 and C20:5), rather than by saturated acids (C14:0, C16:0, C18:0). Increasing the extracellular concentration of albumin from 30 microM to 1 mM displaces PAP-1 activity from the membrane fraction. Sphingosine, but not staurosporine, can inhibit the redistribution of PAP-1 activity induced by oleate. The amphiphilic amines, sphingosine, chlorpromazine and propranolol, also decrease membrane-bound PAP-1 activity in the absence of fatty acids, but they do not alter, significantly, the activity of the cytosolic PAP-1. In the presence of 1 mM oleate, sphingosine, chlorpromazine and propranolol decrease the translocation of PAP-1 from the cytosol to the membranes. The phosphohydrolase activity, which is insensitive to N-ethylmaleimide (PAP-2), is specifically located in the plasma membrane (Jamal, Z., Martin, A., Gomez-Muñoz, A. and Brindley, D.N. (1991) J. Biol. Chem. 266, 2988-2996) and it is not stimulated by Mg2+. Saturated fatty acids, albumin, sphingosine and propranolol have no significant effects on PAP-2 activity. However, chlorpromazine decreases PAP-2 activity by about 14%. Linolenate, arachidonate and eicosapentaenoate at 1 mM also produced small (7-10%) decreases in PAP-2 activity. It is proposed that both PAP-1 and PAP-2 activities may be involved in signal transduction, although the main function of PAP-1 seems to be involved in the synthesis of glycerolipids.
在与0.1 mM白蛋白孵育的培养大鼠肝细胞中,测定了两种磷脂酸磷酸水解酶的活性。被N - 乙基马来酰亚胺抑制的活性(PAP - 1)存在于胞质和膜组分中。PAP - 1活性受Mg2 +刺激,并且在相对低浓度(0.5 - 1 mM)的脂肪酸作用下,它可以从胞质转运至膜上。此外,较高浓度(1 - 3 mM)的脂肪酸会导致PAP - 1总活性增加。肝细胞中PAP - 1活性的转运优先由不饱和脂肪酸(C18:1、C18:2、C18:3、C20:4和C20:5)促进,而非饱和脂肪酸(C14:0、C16:0、C18:0)。将细胞外白蛋白浓度从30 microM增加到1 mM会使PAP - 1活性从膜组分中转移出来。鞘氨醇而非星形孢菌素,可以抑制油酸诱导的PAP - 1活性重新分布。两亲性胺类,鞘氨醇、氯丙嗪和普萘洛尔,在不存在脂肪酸的情况下也会降低膜结合的PAP - 1活性,但它们对胞质PAP - 1的活性没有显著影响。在存在1 mM油酸的情况下,鞘氨醇、氯丙嗪和普萘洛尔会减少PAP - 1从胞质到膜的转运。对N - 乙基马来酰亚胺不敏感的磷酸水解酶活性(PAP - 2)特异性地存在于质膜中(贾马尔,Z.,马丁,A.,戈麦斯 - 穆尼奥斯,A.和布林德利,D.N.(1991)《生物化学杂志》266,2988 - 2996),并且不受Mg2 +刺激。饱和脂肪酸、白蛋白、鞘氨醇和普萘洛尔对PAP - 2活性没有显著影响。然而,氯丙嗪使PAP - 2活性降低约14%。1 mM的亚麻酸、花生四烯酸和二十碳五烯酸也会使PAP - 2活性产生小幅度(7 - 10%)的降低。有人提出,PAP - 1和PAP - 2活性可能都参与信号转导,尽管PAP - 1的主要功能似乎与甘油olipids的合成有关。