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α-actinin accounts for the bioactivity of actin preparations in inducing STAT target genes in Drosophila melanogaster

机译:α-肌动蛋白说明肌动蛋白制剂在果蝇中诱导STAT靶基因的生物活性

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Damage-associated molecular patterns (DAMPs) are molecules exposed or released by dead cells that trigger or modulate immunity and tissue repair. In vertebrates, the cytoskeletal component F-actin is a DAMP specifically recognised by DNGR-1, an innate immune receptor. Previously we suggested that actin is also a DAMP in Drosophila melanogaster by inducing STAT-dependent genes (Srinivasan et al., 2016). Here, we revise that conclusion and report that α-actinin is far more potent than actin at inducing the same STAT response and can be found in trace amounts in actin preparations. Recombinant expression of actin or α-actinin in bacteria demonstrated that only α-actinin could drive the expression of STAT target genes in Drosophila. The response to injected α-actinin required the same signalling cascade that we had identified in our previous work using actin preparations. Taken together, these data indicate that α-actinin rather than actin drives STAT activation when injected into Drosophila.
机译:损伤相关分子模式(DAMP)是由死细胞暴露或释放的分子,它们触发或调节免疫力和组织修复。在脊椎动物中,细胞骨架成分F-肌动蛋白是DAMP被先天性免疫受体DNGR-1特异性识别。以前我们通过诱导STAT依赖性基因暗示肌动蛋白也是果蝇中的DAMP(Srinivasan et al。,2016)。在这里,我们修改该结论并报告说,α-肌动蛋白在诱导相同的STAT反应方面比肌动蛋白有效得多,并且可以在肌动蛋白制剂中找到微量。肌动蛋白或α-肌动蛋白在细菌中的重组表达表明,只有α-肌动蛋白才能驱动果蝇中的STAT靶基因的表达。对注射的α-肌动蛋白的反应需要与我们先前使用肌动蛋白制剂进行的研究相同的信号级联反应。总而言之,这些数据表明当注入果蝇中时,α-肌动蛋白而不是肌动蛋白驱动STAT激活。

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