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

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 pat...

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Autores principales: Canas, Jorge J., Liang, Dong, Saxena, Vijay, Hooks, Jenaya, Arregui, Samuel W., Gao, Hongyu, Liu, Yunlong, Kish, Danielle, Linn, Sarah C., Bdeir, Khalil, Cines, Douglas B., Fairchild, Robert L., Spencer, John D., Schwaderer, Andrew L., Hains, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546544/
https://www.ncbi.nlm.nih.gov/pubmed/36161923
http://dx.doi.org/10.1073/pnas.2206515119
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author Canas, Jorge J.
Liang, Dong
Saxena, Vijay
Hooks, Jenaya
Arregui, Samuel W.
Gao, Hongyu
Liu, Yunlong
Kish, Danielle
Linn, Sarah C.
Bdeir, Khalil
Cines, Douglas B.
Fairchild, Robert L.
Spencer, John D.
Schwaderer, Andrew L.
Hains, David S.
author_facet Canas, Jorge J.
Liang, Dong
Saxena, Vijay
Hooks, Jenaya
Arregui, Samuel W.
Gao, Hongyu
Liu, Yunlong
Kish, Danielle
Linn, Sarah C.
Bdeir, Khalil
Cines, Douglas B.
Fairchild, Robert L.
Spencer, John D.
Schwaderer, Andrew L.
Hains, David S.
author_sort Canas, Jorge J.
collection PubMed
description 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.
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spelling pubmed-95465442023-03-26 Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge Canas, Jorge J. Liang, Dong Saxena, Vijay Hooks, Jenaya Arregui, Samuel W. Gao, Hongyu Liu, Yunlong Kish, Danielle Linn, Sarah C. Bdeir, Khalil Cines, Douglas B. Fairchild, Robert L. Spencer, John D. Schwaderer, Andrew L. Hains, David S. Proc Natl Acad Sci U S A Biological Sciences 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. National Academy of Sciences 2022-09-26 2022-10-04 /pmc/articles/PMC9546544/ /pubmed/36161923 http://dx.doi.org/10.1073/pnas.2206515119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Canas, Jorge J.
Liang, Dong
Saxena, Vijay
Hooks, Jenaya
Arregui, Samuel W.
Gao, Hongyu
Liu, Yunlong
Kish, Danielle
Linn, Sarah C.
Bdeir, Khalil
Cines, Douglas B.
Fairchild, Robert L.
Spencer, John D.
Schwaderer, Andrew L.
Hains, David S.
Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge
title Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge
title_full Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge
title_fullStr Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge
title_full_unstemmed Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge
title_short Human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic Escherichia coli challenge
title_sort human neutrophil peptides 1-3 protect the murine urinary tract from uropathogenic escherichia coli challenge
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9546544/
https://www.ncbi.nlm.nih.gov/pubmed/36161923
http://dx.doi.org/10.1073/pnas.2206515119
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