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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Involvement of group VIA calcium-independent phospholipase A2 in macrophage engulfment of hydrogen peroxide-treated U937 cells.
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Involvement of group VIA calcium-independent phospholipase A2 in macrophage engulfment of hydrogen peroxide-treated U937 cells.

机译:VIA组不依赖钙的磷脂酶A2参与过氧化氢处理的U937细胞的巨噬细胞吞噬。

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摘要

Hydrogen peroxide-induced apoptosis of U937 cells results in substantial hydrolysis of membrane phospholipids by calcium-independent group VIA phospholipase A(2) (iPLA(2)-VIA). However, abrogation of cellular iPLA(2)-VIA neither delays nor decreases apoptosis, suggesting that, beyond a mere destructive role, iPLA(2)-VIA may serve other specific roles. In this study, we report that phagocytosis of apoptosing U937 cells by macrophages is blunted if the cells are depleted of iPLA(2)-VIA by treatment with an inhibitor or an antisense oligonucleotide, and it is augmented by overexpression of iPLA(2)-VIA in the dying cells. Thus, the magnitude of macrophage phagocytosis correlates with the level of iPLA(2)-VIA activity of the dying cells. Eliminating by antisense oligonucleotide technology of cytosolic group IVA phospholipase A(2) does not attenuate phagocytosis of U937 dying cells by macrophages. Incubation of U937 cells with different fatty acids has no effect on either the extent of hydrogen peroxide-induced apoptosis or the degree of phagocytosis of the dying cells by macrophages. However, preincubation of the macrophages with lysophosphatidylcholine before exposing them to the dying cells blocks phagocytosis of the latter. These results indicate that formation of lysophosphatidylcholine by iPLA(2)-VIA in hydrogen peroxide-treated U937 cells to induce apoptosis directly contributes to their efficient clearance by macrophages.
机译:过氧化氢诱导的U937细胞凋亡导致膜独立性钙独立的VIA磷脂酶A(2)(iPLA(2)-VIA)膜磷脂的大量水解。但是,细胞iPLA(2)-VIA的废除既不会延迟也不会减少细胞凋亡,这表明,除了单纯的破坏作用之外,iPLA(2)-VIA可能还发挥其他特定作用。在这项研究中,我们报告说,如果通过用抑制剂或反义寡核苷酸处理使细胞中的iPLA(2)-VIA耗尽,则巨噬细胞对U937细胞凋亡的吞噬作用就会减弱,并且由于iPLA(2)-的过表达而增强了吞噬作用。 VIA在垂死的细胞中。因此,巨噬细胞吞噬作用的大小与垂死细胞的iPLA(2)-VIA活性水平相关。通过反义寡核苷酸技术消除胞质基团IVA磷脂酶A(2)不会减弱巨噬细胞对U937垂死细胞的吞噬作用。用不同的脂肪酸孵育U937细胞对过氧化氢诱导的细胞凋亡程度或巨噬细胞对垂死细胞的吞噬作用都没有影响。但是,巨噬细胞与溶血磷脂酰胆碱预孵育后再暴露于垂死的细胞中会阻止后者的吞噬作用。这些结果表明,由iPLA(2)-VIA在过氧化氢处理的U937细胞中诱导溶细胞凋亡的溶血磷脂酰胆碱直接有助于其被巨噬细胞有效清除。

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