Liao Peng, Jia-Wei Chen, Yuan-Zhuo Chen, Chi Zhang, Si-Hong Shen, Meng-Zhu Liu, Yang Fan, Shi-Qin Yang, Xiu-Zhen Zhang, Wei Wang, Xiao-Shuai Gao, Xing-Peng Di, Yu-Cheng Ma, Xiao Zeng, Hong Shen, Xi Jin, De-Yi Luo
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{"title":"UPK3A+ umbrella cell damage mediated by TLR3–NR2F6 triggers programmed destruction of urothelium in Hunner-type interstitial cystitis/painful bladder syndrome","authors":"Liao Peng, Jia-Wei Chen, Yuan-Zhuo Chen, Chi Zhang, Si-Hong Shen, Meng-Zhu Liu, Yang Fan, Shi-Qin Yang, Xiu-Zhen Zhang, Wei Wang, Xiao-Shuai Gao, Xing-Peng Di, Yu-Cheng Ma, Xiao Zeng, Hong Shen, Xi Jin, De-Yi Luo","doi":"10.1002/path.6275","DOIUrl":null,"url":null,"abstract":"<p>Urothelial damage and barrier dysfunction emerge as the foremost mechanisms in Hunner-type interstitial cystitis/bladder pain syndrome (HIC). Although treatments aimed at urothelial regeneration and repair have been employed, their therapeutic effectiveness remains limited due to the inadequate understanding of specific cell types involved in damage and the lack of specific molecular targets within these mechanisms. Therefore, we harnessed single-cell RNA sequencing to elucidate the heterogeneity and developmental trajectory of urothelial cells within HIC bladders. Through reclustering, we identified eight distinct clusters of urothelial cells. There was a significant reduction in UPK3A<sup>+</sup> umbrella cells and a simultaneous increase in progenitor-like pluripotent cells (PPCs) within the HIC bladder. Pseudotime analysis of the urothelial cells in the HIC bladder revealed that cells faced challenges in differentiating into UPK3A<sup>+</sup> umbrella cells, while PPCs exhibited substantial proliferation to compensate for the loss of UPK3A<sup>+</sup> umbrella cells. The urothelium in HIC remains unrepaired, despite the substantial proliferation of PPCs. Thus, we propose that inhibiting the pivotal signaling pathways responsible for the injury to UPK3A<sup>+</sup> umbrella cells is paramount for restoring the urothelial barrier and alleviating lower urinary tract symptoms in HIC patients. Subsequently, we identified key molecular pathways (TLR3 and NR2F6) associated with the injury of UPK3A<sup>+</sup> umbrella cells in HIC urothelium. Finally, we conducted <i>in vitro</i> and <i>in vivo</i> experiments to confirm the potential of the TLR3–NR2F6 axis as a promising therapeutic target for HIC. These findings hold the potential to inhibit urothelial injury, providing promising clues for early diagnosis and functional bladder self-repair strategies for HIC patients. © 2024 The Pathological Society of Great Britain and Ireland.</p>","PeriodicalId":232,"journal":{"name":"The Journal of Pathology","volume":"263 2","pages":"203-216"},"PeriodicalIF":5.6000,"publicationDate":"2024-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Pathology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/path.6275","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
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Abstract
Urothelial damage and barrier dysfunction emerge as the foremost mechanisms in Hunner-type interstitial cystitis/bladder pain syndrome (HIC). Although treatments aimed at urothelial regeneration and repair have been employed, their therapeutic effectiveness remains limited due to the inadequate understanding of specific cell types involved in damage and the lack of specific molecular targets within these mechanisms. Therefore, we harnessed single-cell RNA sequencing to elucidate the heterogeneity and developmental trajectory of urothelial cells within HIC bladders. Through reclustering, we identified eight distinct clusters of urothelial cells. There was a significant reduction in UPK3A+ umbrella cells and a simultaneous increase in progenitor-like pluripotent cells (PPCs) within the HIC bladder. Pseudotime analysis of the urothelial cells in the HIC bladder revealed that cells faced challenges in differentiating into UPK3A+ umbrella cells, while PPCs exhibited substantial proliferation to compensate for the loss of UPK3A+ umbrella cells. The urothelium in HIC remains unrepaired, despite the substantial proliferation of PPCs. Thus, we propose that inhibiting the pivotal signaling pathways responsible for the injury to UPK3A+ umbrella cells is paramount for restoring the urothelial barrier and alleviating lower urinary tract symptoms in HIC patients. Subsequently, we identified key molecular pathways (TLR3 and NR2F6) associated with the injury of UPK3A+ umbrella cells in HIC urothelium. Finally, we conducted in vitro and in vivo experiments to confirm the potential of the TLR3–NR2F6 axis as a promising therapeutic target for HIC. These findings hold the potential to inhibit urothelial injury, providing promising clues for early diagnosis and functional bladder self-repair strategies for HIC patients. © 2024 The Pathological Society of Great Britain and Ireland.
TLR3-NR2F6介导的UPK3A+伞状细胞损伤引发了Hunner型间质性膀胱炎/膀胱疼痛综合征中尿路上皮的程序性破坏。
尿路上皮损伤和屏障功能障碍是亨纳型间质性膀胱炎/膀胱疼痛综合征(HIC)的主要发病机制。虽然针对尿道再生和修复的治疗方法已被采用,但由于对参与损伤的特定细胞类型了解不足以及缺乏这些机制中的特定分子靶点,其治疗效果仍然有限。因此,我们利用单细胞 RNA 测序来阐明 HIC 膀胱内尿路细胞的异质性和发育轨迹。通过重新聚类,我们确定了八个不同的尿道细胞群。在HIC膀胱内,UPK3A+伞状细胞明显减少,而祖细胞样多能细胞(PPCs)同时增加。对HIC膀胱中的尿路上皮细胞进行的伪时间分析表明,细胞在分化成UPK3A+伞状细胞时面临挑战,而PPCs则表现出大量增殖,以弥补UPK3A+伞状细胞的损失。尽管 PPCs 大量增殖,但 HIC 中的尿路上皮仍未得到修复。因此,我们提出,抑制导致 UPK3A+ 伞状细胞损伤的关键信号通路对于恢复尿路上皮屏障和缓解 HIC 患者的下尿路症状至关重要。随后,我们确定了与 HIC 尿路上皮中 UPK3A+ 伞状细胞损伤相关的关键分子通路(TLR3 和 NR2F6)。最后,我们进行了体外和体内实验,证实了 TLR3-NR2F6 轴作为 HIC 治疗靶点的潜力。这些发现具有抑制尿路上皮损伤的潜力,为 HIC 患者的早期诊断和功能性膀胱自我修复策略提供了有希望的线索。© 2024 大不列颠及爱尔兰病理学会。
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