Cargando…
Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury
Acute kidney injury (AKI) is a common and severe complication of the coronavirus disease 2019 (COVID-19). Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) directly affects the glomerular and tubular epithelial cells to induce AKI; however, its pathophysiology remains unclear. Here, we ex...
Autores principales: | , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415265/ https://www.ncbi.nlm.nih.gov/pubmed/37563112 http://dx.doi.org/10.1038/s41420-023-01584-x |
_version_ | 1785087496017674240 |
---|---|
author | Nakazawa, Daigo Takeda, Yohei Kanda, Masatoshi Tomaru, Utano Ogawa, Haruko Kudo, Takashi Shiratori-Aso, Satoka Watanabe-Kusunoki, Kanako Ueda, Yusho Miyoshi, Atsuko Hattanda, Fumihiko Nishio, Saori Uozumi, Ryo Ishizu, Akihiro Atsumi, Tatsuya |
author_facet | Nakazawa, Daigo Takeda, Yohei Kanda, Masatoshi Tomaru, Utano Ogawa, Haruko Kudo, Takashi Shiratori-Aso, Satoka Watanabe-Kusunoki, Kanako Ueda, Yusho Miyoshi, Atsuko Hattanda, Fumihiko Nishio, Saori Uozumi, Ryo Ishizu, Akihiro Atsumi, Tatsuya |
author_sort | Nakazawa, Daigo |
collection | PubMed |
description | Acute kidney injury (AKI) is a common and severe complication of the coronavirus disease 2019 (COVID-19). Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) directly affects the glomerular and tubular epithelial cells to induce AKI; however, its pathophysiology remains unclear. Here, we explored the underlying mechanisms and therapeutic targets of renal involvement in COVID-19. We developed an in vitro human kidney cellular model, including immortalized tubular epithelial and endothelial cell lines, demonstrating that SARS-CoV-2 directly triggers cell death. To identify the molecular targets in the process of SARS-CoV-2-mediated cell injury, we performed transcriptional analysis using RNA sequencing. Tubular epithelial cells were more prone to dying by SARS-CoV-2 than endothelial cells; however, SARS-CoV-2 did not replicate in renal cells, distinct from VeroE6/transmembrane protease serine 2 cells. Transcriptomic analysis revealed increased inflammatory and immune-related gene expression levels in renal cells incubated with SARS-CoV-2. Toll-like receptor (TLR) 3 in renal cells recognized viral RNA and underwent cell death. Furthermore, analysis of upstream regulators identified several key transcriptional regulators. Among them, inhibition of the interleukin-1 receptor (IL-1R) and TLR4 pathways protects tubular epithelial and endothelial cells from injury via regulation of the signal transducer and activator of transcription protein-3/nuclear factor-kB pathway. Our results reveal that SARS-CoV-2 directly injures renal cells via the proinflammatory response without viral replication, and that IL-1R and TLR4 may be used as therapeutic targets for SARS-CoV-2 mediated kidney injury. |
format | Online Article Text |
id | pubmed-10415265 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104152652023-08-12 Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury Nakazawa, Daigo Takeda, Yohei Kanda, Masatoshi Tomaru, Utano Ogawa, Haruko Kudo, Takashi Shiratori-Aso, Satoka Watanabe-Kusunoki, Kanako Ueda, Yusho Miyoshi, Atsuko Hattanda, Fumihiko Nishio, Saori Uozumi, Ryo Ishizu, Akihiro Atsumi, Tatsuya Cell Death Discov Article Acute kidney injury (AKI) is a common and severe complication of the coronavirus disease 2019 (COVID-19). Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) directly affects the glomerular and tubular epithelial cells to induce AKI; however, its pathophysiology remains unclear. Here, we explored the underlying mechanisms and therapeutic targets of renal involvement in COVID-19. We developed an in vitro human kidney cellular model, including immortalized tubular epithelial and endothelial cell lines, demonstrating that SARS-CoV-2 directly triggers cell death. To identify the molecular targets in the process of SARS-CoV-2-mediated cell injury, we performed transcriptional analysis using RNA sequencing. Tubular epithelial cells were more prone to dying by SARS-CoV-2 than endothelial cells; however, SARS-CoV-2 did not replicate in renal cells, distinct from VeroE6/transmembrane protease serine 2 cells. Transcriptomic analysis revealed increased inflammatory and immune-related gene expression levels in renal cells incubated with SARS-CoV-2. Toll-like receptor (TLR) 3 in renal cells recognized viral RNA and underwent cell death. Furthermore, analysis of upstream regulators identified several key transcriptional regulators. Among them, inhibition of the interleukin-1 receptor (IL-1R) and TLR4 pathways protects tubular epithelial and endothelial cells from injury via regulation of the signal transducer and activator of transcription protein-3/nuclear factor-kB pathway. Our results reveal that SARS-CoV-2 directly injures renal cells via the proinflammatory response without viral replication, and that IL-1R and TLR4 may be used as therapeutic targets for SARS-CoV-2 mediated kidney injury. Nature Publishing Group UK 2023-08-10 /pmc/articles/PMC10415265/ /pubmed/37563112 http://dx.doi.org/10.1038/s41420-023-01584-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Nakazawa, Daigo Takeda, Yohei Kanda, Masatoshi Tomaru, Utano Ogawa, Haruko Kudo, Takashi Shiratori-Aso, Satoka Watanabe-Kusunoki, Kanako Ueda, Yusho Miyoshi, Atsuko Hattanda, Fumihiko Nishio, Saori Uozumi, Ryo Ishizu, Akihiro Atsumi, Tatsuya Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury |
title | Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury |
title_full | Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury |
title_fullStr | Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury |
title_full_unstemmed | Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury |
title_short | Inhibition of Toll-like receptor 4 and Interleukin-1 receptor prevent SARS-CoV-2 mediated kidney injury |
title_sort | inhibition of toll-like receptor 4 and interleukin-1 receptor prevent sars-cov-2 mediated kidney injury |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415265/ https://www.ncbi.nlm.nih.gov/pubmed/37563112 http://dx.doi.org/10.1038/s41420-023-01584-x |
work_keys_str_mv | AT nakazawadaigo inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT takedayohei inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT kandamasatoshi inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT tomaruutano inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT ogawaharuko inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT kudotakashi inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT shiratoriasosatoka inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT watanabekusunokikanako inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT uedayusho inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT miyoshiatsuko inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT hattandafumihiko inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT nishiosaori inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT uozumiryo inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT ishizuakihiro inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury AT atsumitatsuya inhibitionoftolllikereceptor4andinterleukin1receptorpreventsarscov2mediatedkidneyinjury |