Kurosawa M, Uno D, Hanawa K, Kobayashi S
First Department of Internal Medicine, Gunma University School of Medicine, Japan.
Allergy. 1990 May;45(4):262-7. doi: 10.1111/j.1398-9995.1990.tb00494.x.
Rat mast cell granules were obtained by homogenization of highly purified rat mast cells and isolated in a Percoll gradient. Diphosphoinositide (DPI) synthesis in rat mast cell granules was assayed by measuring the incorporation of 32P from [gamma 32P] ATP into DPI in the absence of exogenous phosphatidylinositol (PI). Lipids were isolated with methanol/chloroform/HCl and were separated by thin-layer chromatography on oxalic acid impregnated silica gel plates. DPI areas were identified by staining with iodine, scraped and measured for 32P radioactivity. The addition of polyamines, spermine and spermidine, to the granules caused an increase of DPI synthesis, which can be catalyzed by PI kinase. This effect of polyamines in the DPI synthesis was in a dose-dependent manner and maximal effects were observed at 1 mM spermine and 10 mM spermidine, respectively.
通过对高度纯化的大鼠肥大细胞进行匀浆获得大鼠肥大细胞颗粒,并在Percoll梯度中进行分离。在不存在外源性磷脂酰肌醇(PI)的情况下,通过测量[γ-32P]ATP中的32P掺入二磷酸肌醇(DPI)来测定大鼠肥大细胞颗粒中DPI的合成。用甲醇/氯仿/盐酸分离脂质,并在草酸浸渍的硅胶板上通过薄层色谱法进行分离。通过碘染色鉴定DPI区域,刮下并测量32P放射性。向颗粒中添加多胺、精胺和亚精胺会导致DPI合成增加,这可由PI激酶催化。多胺对DPI合成的这种作用呈剂量依赖性,分别在1 mM精胺和10 mM亚精胺时观察到最大效应。