Scar-associated macrophages and biliary epithelial cells interaction exacerbates hepatic fibrosis in biliary atresia.

IF 3.1 3区 医学 Q1 PEDIATRICS
Xin Li, Tengfei Li, Shaowen Liu, Yilin Zhao, Yuqiang Chen, Alimujiang Abudureyimu, Shujian Zhang, Liang Ge, Qianhui Yang, Yu Meng, Jiaying Liu, Jiayinaxi Musha, Jianghua Zhan
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引用次数: 0

Abstract

Background: Biliary atresia (BA) is a severe pediatric biliary disorder characterized by the progressive obstruction of liver bile ducts. In the absence of treatment, fibrosis advances rapidly in most affected children. Despite the identification of various factors contributing to fibrosis progression, comprehensive investigations into the microenvironmental alterations within the liver are still scarce.

Methods: Single-cell RNA sequencing (scRNA-seq) was conducted on two normal tissues adjacent to liver tumors, two choledochal cyst liver tissues, and four BA liver tissues. This analysis, combined with spatial localization data, elucidated the heterogeneity of the livers affected by BA. Ultimately, a diagnostic model for BA was developed, leveraging high-resolution fibrosis-related gene signatures.

Results: We identified scar-associated macrophages (SAMs) originating from monocytes, which played a pivotal role in fibrosis progression and may be implicated in the epithelial-mesenchymal transition (EMT) of biliary epithelial cells (BECs). Furthermore, the hub genes CD96, EVL, S100A6, and S100A11 were found to be upregulated in SAMs and regulatory T cells (Tregs), aiding in the diagnosis of BA.

Conclusion: SAMs and BECs not only exhibited a pro-fibrotic phenotype but also co-localized within fibrotic regions. Their interaction may facilitate the activation of EMT, highlighting a potential therapeutic target for BA treatment.

Impact: Analysis of the immune landscape: Through single-cell and spatial transcriptomic techniques, the paper reveals the complex immune landscape associated with BA fibrosis. Exploration of new therapeutic targets: This paper reveals that SAMs can promote the progression of liver fibrosis by regulating the EMT conversion of BECs, opening up a new therapeutic approach. Application of diagnostic markers: The paper identifies biomarkers that may improve early diagnostic accuracy and postoperative prognosis and recommends their incorporation into clinical practice.

疤痕相关巨噬细胞和胆道上皮细胞的相互作用加剧了胆道闭锁的肝纤维化。
背景:胆道闭锁(BA)是一种以肝胆管进行性梗阻为特征的严重小儿胆道疾病。在缺乏治疗的情况下,大多数受影响儿童的纤维化进展迅速。尽管确定了促进纤维化进展的各种因素,但对肝脏内微环境改变的全面研究仍然很少。方法:对2例肝肿瘤旁正常组织、2例胆总管囊肿肝组织和4例BA肝组织进行单细胞RNA测序(scRNA-seq)。该分析结合空间定位数据,阐明了BA影响肝脏的异质性。最终,利用高分辨率的纤维化相关基因特征,开发了BA的诊断模型。结果:我们发现了源自单核细胞的疤痕相关巨噬细胞(SAMs),它在纤维化进程中起关键作用,并可能与胆道上皮细胞(BECs)的上皮-间质转化(EMT)有关。此外,中心基因CD96、EVL、S100A6和S100A11在SAMs和调节性T细胞(Tregs)中表达上调,有助于BA的诊断。结论:SAMs和BECs不仅表现出促纤维化表型,而且在纤维化区域内共定位。它们的相互作用可能促进EMT的激活,这突出了BA治疗的潜在治疗靶点。影响:免疫景观分析:通过单细胞和空间转录组学技术,本文揭示了与BA纤维化相关的复杂免疫景观。新的治疗靶点探索:本文揭示了SAMs可通过调节BECs的EMT转化促进肝纤维化的进展,开辟了新的治疗途径。诊断标志物的应用:本文确定了可提高早期诊断准确性和术后预后的生物标志物,并建议将其纳入临床实践。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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