Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge

Author:

Canas Jorge J.12ORCID,Liang Dong1,Saxena Vijay1ORCID,Hooks Jenaya1,Arregui Samuel W.1,Gao Hongyu3,Liu Yunlong3,Kish Danielle4,Linn Sarah C.5,Bdeir Khalil67,Cines Douglas B.67ORCID,Fairchild Robert L.4,Spencer John D.8ORCID,Schwaderer Andrew L.19ORCID,Hains David S.129ORCID

Affiliation:

1. Wells Center for Pediatric Research, Department of Pediatrics, Indiana University School of Medicine, Indianapolis, IN 46202

2. Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN 46202

3. Center for Computational Biology and Bioinformatics, Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202

4. Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic, Cleveland, OH 44195

5. Kidney and Urinary Tract Center at Nationwide Children’s, The Ohio State University College of Veterinary Medicine, Columbus, OH 43205

6. Department of Pathology and Laboratory Medicine, University of Pennsylvania-Perelman School of Medicine, Philadelphia, PA 19104

7. Department of Medicine, University of Pennsylvania-Perelman School of Medicine, Philadelphia, PA 19104

8. Division of Nephrology and Hypertension, Kidney and Urinary Tract Center at Nationwide Children’s, Columbus, OH 43205

9. Division of Pediatric Nephrology, Riley Hospital for Children, Indianapolis, IN 46202

Abstract

Antimicrobial peptides (AMPs) are critical to the protection of the urinary tract of humans and other animals from pathogenic microbial invasion. AMPs rapidly destroy pathogens by disrupting microbial membranes and/or augmenting or inhibiting the host immune system through a variety of signaling pathways. We have previously demonstrated that alpha-defensins 1-3 ( DEFA1A3 ) are AMPs expressed in the epithelial cells of the human kidney collecting duct in response to uropathogens. We also demonstrated that DNA copy number variations in the DEFA1A3 locus are associated with UTI and pyelonephritis risk. Because DEFA1A3 is not expressed in mice, we utilized human DEFA1A3 gene transgenic mice ( DEFA 4/4 ) to further elucidate the biological relevance of this locus in the murine urinary tract. We demonstrate that the kidney transcriptional and translational expression pattern is similar in humans and the human gene transgenic mouse upon uropathogenic Escherichia coli (UPEC) stimulus in vitro and in vivo. We also demonstrate transgenic human DEFA 4/4 gene mice are protected from UTI and pyelonephritis under various UPEC challenges. This study serves as the foundation to start the exploration of manipulating the DEFA1A3 locus and alpha-defensins 1-3 expression as a potential therapeutic target for UTIs and other infectious diseases.

Funder

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Secretory leukocyte protease inhibitor protects against severe urinary tract infection in mice;mBio;2024-01-25

2. Intercalated cell function, kidney innate immunity, and urinary tract infections;Pflügers Archiv - European Journal of Physiology;2024-01-16

3. Immune defenses in the urinary tract;Trends in Immunology;2023-09

4. Mechanisms and regulation of defensins in host defense;Signal Transduction and Targeted Therapy;2023-08-14

5. Uropathogen and host responses in pyelonephritis;Nature Reviews Nephrology;2023-07-21

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