Ductular reaction-associated neutrophils promote biliary epithelium proliferation in chronic liver disease

上皮 胆道疾病 慢性肝病 医学 病理 胃肠病学 肝硬化
作者
Sílvia Ariño,Beatriz Aguilar‐Bravo,Mar Coll,Woo‐Yong Lee,Moritz Peiseler,Paula Cantallops-Vilà,Laura Sererols-Viñas,Raquel A. Martínez-García de la Torre,Celia Martínez–Sánchez,Jordi Pedragosa,Laura Zanatto,Jordi Gratacós‐Ginès,Elisa Pose,Delia Blaya,Xènia Almodóvar,María Fernández-Fernández,Paloma Ruiz-Blázquez,Juan José Lozano,Silvia Affò,Anna M. Planas
出处
期刊:Journal of Hepatology [Elsevier BV]
卷期号:79 (4): 1025-1036 被引量:57
标识
DOI:10.1016/j.jhep.2023.05.045
摘要

Background & Aims

Ductular reaction expansion is associated with poor prognosis in patients with advanced liver disease. However, the mechanisms promoting biliary cell proliferation are largely unknown. Here, we identify neutrophils as drivers of biliary cell proliferation and the defective wound-healing response.

Methods

The intrahepatic localization of neutrophils was evaluated in patients with chronic liver disease. Neutrophil dynamics were analyzed by intravital microscopy and neutrophil-labeling assays in DDC-treated mice. Neutrophil depletion or inhibition of recruitment was achieved using a Ly6g antibody or a CXCR1/2 inhibitor, respectively. Mice deficient in PAD4 (peptidyl arginine deiminase 4) and ELANE/NE (neutrophil elastase) were used to investigate the mechanisms underlying ductular reaction expansion.

Results

In this study we describe a population of ductular reaction-associated neutrophils (DRANs), which are in direct contact with biliary epithelial cells in chronic liver diseases and whose numbers increased in parallel with disease progression. We show that DRANs are immobilized at the site of ductular reaction for a prolonged period of time. In addition, liver neutrophils display a unique phenotypic and transcriptomic profile, showing a decreased phagocytic capacity and increased oxidative burst. Depletion of neutrophils or inhibition of their recruitment reduces DRANs and the expansion of ductular reaction, while mitigating liver fibrosis and angiogenesis. Mechanistically, neutrophils deficient in PAD4 and ELANE abrogate neutrophil-induced biliary cell proliferation, thus indicating the role of neutrophil extracellular traps and elastase release in ductular reaction expansion.

Conclusions

Overall, our study reveals the accumulation of DRANs as a hallmark of advanced liver disease and a potential therapeutic target to mitigate ductular reaction and the maladaptive wound-healing response.

Impact and implications

Our results indicate that neutrophils are highly plastic and can have an extended lifespan. Moreover, we identify a new role of neutrophils as triggers of expansion of the biliary epithelium. Overall, the results of this study indicate that ductular reaction-associated neutrophils (or DRANs) are new players in the maladaptive tissue-healing response in chronic liver injury and may be a potential target for therapeutic interventions to reduce ductular reaction expansion and promote tissue repair in advanced liver disease.
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