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DNA 基因剂量调控上尿路感染期间肾脏固有免疫反应。

DNA gene-dosage regulates the kidney innate immune response during upper urinary tract infection.

机构信息

Division of Pediatric Nephrology, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.

Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Life Sci Alliance. 2024 Apr 5;7(6). doi: 10.26508/lsa.202302462. Print 2024 Jun.

Abstract

Antimicrobial peptides (AMPs) are host defense effectors with potent neutralizing and immunomodulatory functions against invasive pathogens. The AMPs α-Defensin 1-3/ participate in innate immune responses and influence patient outcomes in various diseases. DNA copy-number variations in have been associated with severity and outcomes in infectious diseases including urinary tract infections (UTIs). Specifically, children with lower DNA copy numbers were more susceptible to UTIs. The mechanism of action by which α-Defensin 1-3/ copy-number variations lead to UTI susceptibility remains to be explored. In this study, we use a previously characterized transgenic knock-in of the human gene mouse to dissect α-Defensin 1-3 gene dose-dependent antimicrobial and immunomodulatory roles during uropathogenic (UPEC) UTI. We elucidate the relationship between kidney neutrophil- and collecting duct intercalated cell-derived α-Defensin 1-3/ expression and UTI. We further describe cooperative effects between α-Defensin 1-3 and other AMPs that potentiate the neutralizing activity against UPEC. Cumulatively, we demonstrate that directly protects against UPEC meanwhile impacting pro-inflammatory innate immune responses in a gene dosage-dependent manner.

摘要

抗菌肽 (AMPs) 是宿主防御效应物,具有针对侵袭性病原体的强大中和和免疫调节功能。α-防御素 1-3/参与先天免疫反应,并影响各种疾病患者的预后。 在 中 DNA 拷贝数变异与传染病(包括尿路感染 (UTI))的严重程度和结局相关。具体来说,DNA 拷贝数较低的儿童更容易发生 UTI。α-防御素 1-3/拷贝数变异导致 UTI 易感性的作用机制仍有待探索。在这项研究中,我们使用之前表征的人类 基因小鼠转基因敲入品系来剖析在尿路感染性大肠埃希菌 (UPEC) UTI 期间,α-防御素 1-3 基因剂量依赖性的抗菌和免疫调节作用。我们阐明了肾脏中性粒细胞和集合管闰细胞衍生的 α-防御素 1-3/表达与 UTI 之间的关系。我们进一步描述了 α-防御素 1-3 与其他 AMP 之间的协同作用,这些协同作用增强了针对 UPEC 的中和活性。总之,我们证明 直接针对 UPEC 起到保护作用,同时以基因剂量依赖的方式影响促炎先天免疫反应。

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