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其分泌 III 型效应蛋白以逃避人细胞中 caspase-4 炎性小体的激活。

deploys type III-secreted effectors to evade caspase-4 inflammasome activation in human cells.

机构信息

Department of Microbiology, University of Pennsylvania, Perelman School of Medicine , Philadelphia, Pennsylvania, USA.

Department of Pathobiology, University of Pennsylvania, School of Veterinary Medicine , Philadelphia, Pennsylvania, USA.

出版信息

mBio. 2023 Oct 31;14(5):e0131023. doi: 10.1128/mbio.01310-23. Epub 2023 Aug 24.

Abstract

are responsible for significant disease burden in humans, ranging from recurrent disease outbreaks (yersiniosis) to pandemics ( plague). Together with rising antibiotic resistance rates, there is a critical need to better understand pathogenesis and host immune mechanisms, as this information will aid in developing improved immunomodulatory therapeutics. Inflammasome responses in human cells are less studied relative to murine models of infection, though recent studies have uncovered key differences in inflammasome responses between mice and humans. Here, we dissect human intestinal epithelial cell and macrophage inflammasome responses to . Our findings provide insight into species- and cell type-specific differences in inflammasome responses to .

摘要

这些病原体在人类中引发了重大疾病负担,包括反复发作的疾病爆发(耶尔森菌病)和大流行(鼠疫)。随着抗生素耐药率的上升,人们迫切需要更好地了解发病机制和宿主免疫机制,因为这些信息将有助于开发改良的免疫调节疗法。与感染的小鼠模型相比,人类细胞中的炎症小体反应的研究较少,但最近的研究揭示了小鼠和人类之间炎症小体反应的关键差异。在这里,我们剖析了人类肠上皮细胞和巨噬细胞对 的炎症小体反应。我们的研究结果为理解 诱导的炎症小体反应在种属和细胞类型特异性方面的差异提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fde/10653943/26d37b8b01d3/mbio.01310-23.f001.jpg

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