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Sweet kiss of dying cell: Sialidase activity on apoptotic cell is able to act toward its neighbors

机译:垂死细胞的甜蜜接吻:凋亡细胞上的唾液酸酶活性能够对其邻居起作用

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Apoptotic cells and subcellular microparticles expose increased sialidase activity on their surfaces, which results from caspase-3 dependent activation of plasma membrane associated Neuraminidase-1 (Neu1). Desialylation of dying cells is also known to promote efferocytosis. The intriguing question remained whether sialidase on the surface of dying cell merely acts on self targets (cis-action), or whether it can also cleave glycoepitopes of neighboring cells (trans-action). Here, we co-incubated human viable and apoptotic Jurkat lymphocytes or neutrophils with human erythrocytes and evaluated their glycoprofile for terminal sialic acids by agglutination assay, flow cytometry, ELISA and dot-blot analyses. Data suggest that erythrocytes were desialylated as soon as 3 hours after co-incubation with apoptotic cells, but not with viable ones. After co-incubation of L929 murine fibroblasts with viable or apoptotic murine L1210 cells the L929 cells gained a desialylated glycoprofile, only after co-incubation with apoptotic cells. Our data suggests that activated sialidase(s) on the surfaces of apoptotic cells are capable to desialylate neighboring cells in trans.
机译:凋亡细胞和亚细胞微粒暴露了唾液酸酶活性增加的表面,这是由caspase-3依赖性的质膜相关神经氨酸酶1(Neu1)活化引起的。还已知垂死细胞的去唾液酸化作用促进胞吞作用。有趣的问题仍然是,垂死细胞表面的唾液酸酶是否仅作用于自身靶标(顺式作用),或者它是否还可以切割邻近细胞的糖表位(反式作用)。在这里,我们与人类红细胞共同孵育了人类存活和凋亡的Jurkat淋巴细胞或嗜中性粒细胞,并通过凝集测定,流式细胞术,ELISA和斑点印迹分析评估了其末端唾液酸的糖谱。数据表明,在与凋亡细胞共孵育后3小时之内,红细胞就被去唾液酸化,但没有与存活细胞共孵育。将L929鼠成纤维细胞与有活力或凋亡的鼠L1210细胞共孵育后,仅在与凋亡细胞共孵育后,L929细胞才能获得脱唾液酸化的糖分布。我们的数据表明,凋亡细胞表面的活化唾液酸酶能够反式脱唾液酸化邻近细胞。

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