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Local Necrotic Cells Trigger Systemic Immune Activation via Gut Microbiome Dysbiosis in Drosophila

机译:局部坏死细胞通过果蝇中的肠道微生物组脱菌病引发全身免疫活化

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Necrotic cells elicit an inflammatory response through their endogenous factors with damage-associated molecular patterns. Blocking apoptosis in Drosophila wings leads to the necrosis-driven systemic immune response by unknown mechanisms. Here, we demonstrate that immune activation in response to necrotic cells is mediated by commensal gut microbiota. Removing the microbiome attenuates hyperactivation of the innate immune signaling IMD pathway in necrosis-induced flies. Necrotic cells in wings trigger Gluconobacter expansion in the gut. An isolated Gluconobacter sp. strain is sufficient for pathological IMD activation in necrosis-induced flies, while it is not inflammatory for control animals. In addition, bacterial colonization shifts the host metabolome and shortens the lifespan of necrosis-induced flies. This study shows that local necrosis triggers a pathological systemic inflammatory response through interaction between the host and the dysbiotic gut microbiome.
机译:坏死细胞通过其内源性因子引发炎症反应,其具有损伤相关的分子模式。通过未知机制阻断果蝇翅膀的细胞凋亡导致坏死驱动的系统免疫应答。这里,我们证明响应于坏死细胞的免疫激活是由非共和肠道微生物瘤介导的。去除微生物组衰减在坏死诱导的苍蝇中的先天免疫信号传导IMD途径的多动激活。翼中的坏死细胞触发肠道中的葡糖杆菌膨胀。一个孤立的葡糖杆菌sp。菌株足以用于坏死诱导的苍蝇的病理IMD活化,而对照动物不是炎症。此外,细菌殖民化转移宿主代谢物,缩短坏死诱导的苍蝇的寿命。本研究表明,局部坏死通过宿主和歧疲力学肠道微生物组之间的相互作用来触发病理全身炎症反应。

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