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A single-cell landscape of triptolide-associated testicular toxicity in mice

Triptolide is a key active component of the widely used traditional Chinese herb medicine Tripterygium wilfordii Hook. F. Although triptolide exerts multiple biological activities and shows promising efficacy in treating inflammatory-related diseases, its well-known safety issues, especially reprodu...

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Autores principales: Zhang, Wei, Xia, Siyu, Ou, Jinhuan, Cao, Min, Cheng, Guangqing, Li, Zhijie, Wang, Jigang, Yang, Chuanbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Xi'an Jiaotong University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499588/
https://www.ncbi.nlm.nih.gov/pubmed/37719193
http://dx.doi.org/10.1016/j.jpha.2023.04.006
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author Zhang, Wei
Xia, Siyu
Ou, Jinhuan
Cao, Min
Cheng, Guangqing
Li, Zhijie
Wang, Jigang
Yang, Chuanbin
author_facet Zhang, Wei
Xia, Siyu
Ou, Jinhuan
Cao, Min
Cheng, Guangqing
Li, Zhijie
Wang, Jigang
Yang, Chuanbin
author_sort Zhang, Wei
collection PubMed
description Triptolide is a key active component of the widely used traditional Chinese herb medicine Tripterygium wilfordii Hook. F. Although triptolide exerts multiple biological activities and shows promising efficacy in treating inflammatory-related diseases, its well-known safety issues, especially reproductive toxicity has aroused concerns. However, a comprehensive dissection of triptolide-associated testicular toxicity at single cell resolution is still lacking. Here, we observed testicular toxicity after 14 days of triptolide exposure, and then constructed a single-cell transcriptome map of 59,127 cells in mouse testes upon triptolide-treatment. We identified triptolide-associated shared and cell-type specific differentially expressed genes, enriched pathways, and ligand-receptor pairs in different cell types of mouse testes. In addition to the loss of germ cells, our results revealed increased macrophages and the inflammatory response in triptolide-treated mouse testes, suggesting a critical role of inflammation in triptolide-induced testicular injury. We also found increased reactive oxygen species (ROS) signaling and downregulated pathways associated with spermatid development in somatic cells, especially Leydig and Sertoli cells, in triptolide-treated mice, indicating that dysregulation of these signaling pathways may contribute to triptolide-induced testicular toxicity. Overall, our high-resolution single-cell landscape offers comprehensive information regarding triptolide-associated gene expression profiles in major cell types of mouse testes at single cell resolution, providing an invaluable resource for understanding the underlying mechanism of triptolide-associated testicular injury and additional discoveries of therapeutic targets of triptolide-induced male reproductive toxicity.
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spelling pubmed-104995882023-09-15 A single-cell landscape of triptolide-associated testicular toxicity in mice Zhang, Wei Xia, Siyu Ou, Jinhuan Cao, Min Cheng, Guangqing Li, Zhijie Wang, Jigang Yang, Chuanbin J Pharm Anal Original Article Triptolide is a key active component of the widely used traditional Chinese herb medicine Tripterygium wilfordii Hook. F. Although triptolide exerts multiple biological activities and shows promising efficacy in treating inflammatory-related diseases, its well-known safety issues, especially reproductive toxicity has aroused concerns. However, a comprehensive dissection of triptolide-associated testicular toxicity at single cell resolution is still lacking. Here, we observed testicular toxicity after 14 days of triptolide exposure, and then constructed a single-cell transcriptome map of 59,127 cells in mouse testes upon triptolide-treatment. We identified triptolide-associated shared and cell-type specific differentially expressed genes, enriched pathways, and ligand-receptor pairs in different cell types of mouse testes. In addition to the loss of germ cells, our results revealed increased macrophages and the inflammatory response in triptolide-treated mouse testes, suggesting a critical role of inflammation in triptolide-induced testicular injury. We also found increased reactive oxygen species (ROS) signaling and downregulated pathways associated with spermatid development in somatic cells, especially Leydig and Sertoli cells, in triptolide-treated mice, indicating that dysregulation of these signaling pathways may contribute to triptolide-induced testicular toxicity. Overall, our high-resolution single-cell landscape offers comprehensive information regarding triptolide-associated gene expression profiles in major cell types of mouse testes at single cell resolution, providing an invaluable resource for understanding the underlying mechanism of triptolide-associated testicular injury and additional discoveries of therapeutic targets of triptolide-induced male reproductive toxicity. Xi'an Jiaotong University 2023-08 2023-04-14 /pmc/articles/PMC10499588/ /pubmed/37719193 http://dx.doi.org/10.1016/j.jpha.2023.04.006 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Zhang, Wei
Xia, Siyu
Ou, Jinhuan
Cao, Min
Cheng, Guangqing
Li, Zhijie
Wang, Jigang
Yang, Chuanbin
A single-cell landscape of triptolide-associated testicular toxicity in mice
title A single-cell landscape of triptolide-associated testicular toxicity in mice
title_full A single-cell landscape of triptolide-associated testicular toxicity in mice
title_fullStr A single-cell landscape of triptolide-associated testicular toxicity in mice
title_full_unstemmed A single-cell landscape of triptolide-associated testicular toxicity in mice
title_short A single-cell landscape of triptolide-associated testicular toxicity in mice
title_sort single-cell landscape of triptolide-associated testicular toxicity in mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10499588/
https://www.ncbi.nlm.nih.gov/pubmed/37719193
http://dx.doi.org/10.1016/j.jpha.2023.04.006
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