Nakatani N, Uozumi N, Kume K, Murakami M, Kudo I, Shimizu T
Department of Biochemistry and Molecular Biology, Faculty of Medicine, The University of Tokyo, Tokyo 113-0033, Japan.
Biochem J. 2000 Dec 1;352 Pt 2(Pt 2):311-7.
Cytosolic phospholipase A(2) (cPLA(2)) plays a critical role in mast-cell-related allergic responses [Uozumi, Kume, Nagase, Nakatani, Ishii, Tashiro, Komagata, Maki, Ikuta, Ouchi et al. (1997) Nature (London) 390, 618-622]. Bone-marrow-derived mast cells from mice lacking cPLA(2) (cPLA(-/-)(2) mice) were used in order to better define the role of cPLA(2) in the maturation and degranulation of such cells. Cross-linking of high-affinity receptors for IgE (FcepsilonRI) on cells from cPLA(-/-)(2) mice led to the release of negligible amounts of arachidonic acid or its metabolites, the cysteinyl leukotrienes and prostaglandin D(2), indicating an essential role for cPLA(2) in the production of these allergic and pro-inflammatory lipid mediators. In addition, the histamine content of the mast cells and its release from the cells were reduced to 60%. While these results are in agreement with a reduced anaphylactic phenotype of cPLA(-/-)(2) mice, the ratios of release of histamine and beta-hexosaminidase were, paradoxically, significantly higher for cells from cPLA(-/-)(2) mice than for those from wild-type mice. Consistently, IgE-induced calcium influx in mast cells was greater and more prolonged in cells from cPLA(-/-)(2) mice than in those from wild-type mice. Thus the loss of cPLA(2) not only diminishes the release of lipid mediators, but also alters degranulation. While the overall effect is still a decrease in the release of mast cell mediators, explaining the in vivo findings, the present study proposes a novel link between cPLA(2) and the degranulation machinery.
胞质型磷脂酶A2(cPLA2)在肥大细胞相关的过敏反应中起关键作用[上泉、久米、长濑、中谷、石井、田代、小笠原、牧木、育田、大内等(1997年),《自然》(伦敦)390卷,618 - 622页]。为了更好地确定cPLA2在此类细胞成熟和脱颗粒过程中的作用,使用了来自缺乏cPLA2的小鼠(cPLA2-/-小鼠)的骨髓来源肥大细胞。cPLA2-/-小鼠细胞上的IgE高亲和力受体(FcepsilonRI)交联后,花生四烯酸或其代谢产物半胱氨酰白三烯和前列腺素D2的释放量可忽略不计,这表明cPLA2在这些过敏和促炎脂质介质的产生中起重要作用。此外,肥大细胞的组胺含量及其从细胞中的释放量降低至60%。虽然这些结果与cPLA2-/-小鼠过敏反应表型降低一致,但矛盾的是,cPLA2-/-小鼠细胞的组胺和β-己糖胺酶释放率显著高于野生型小鼠细胞。同样,IgE诱导的肥大细胞钙内流在cPLA2-/-小鼠细胞中比野生型小鼠细胞更大且更持久。因此,cPLA2的缺失不仅减少了脂质介质的释放,还改变了脱颗粒过程。虽然总体效果仍是肥大细胞介质释放减少,这解释了体内研究结果,但本研究提出了cPLA2与脱颗粒机制之间的新联系。