Sande-Melon Marcos, Bergemann David, Fernández-Lajarín Miriam, González-Rosa Juan Manuel, Cox Andrew G
Peter MacCallum Cancer Centre, Melbourne, Victoria, 3000, Australia.
The Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, Victoria, 3000, Australia.
bioRxiv. 2024 Jun 17:2023.07.24.550437. doi: 10.1101/2023.07.24.550437.
The liver is a remarkable organ that can regenerate in response to injury. Depending on the extent of injury, the liver can undergo compensatory hyperplasia or fibrosis. Despite decades of research, the molecular mechanisms underlying these processes are poorly understood. Here, we developed a new model to study liver regeneration based on cryoinjury. To visualise liver regeneration at cellular resolution, we adapted the CUBIC tissue-clearing approach. Hepatic cryoinjury induced a localised necrotic and apoptotic lesion characterised by inflammation and infiltration of innate immune cells. Following this initial phase, we observed fibrosis, which resolved as regeneration re-established homeostasis in 30 days. Importantly, this approach enables the comparison of healthy and injured parenchyma with an individual animal, providing unique advantages to previous models. In summary, the hepatic cryoinjury model provides a fast and reproducible method for studying the cellular and molecular pathways underpinning fibrosis and liver regeneration.
肝脏是一个非凡的器官,能够对损伤做出再生反应。根据损伤程度,肝脏可发生代偿性增生或纤维化。尽管经过了数十年的研究,但对这些过程背后的分子机制仍知之甚少。在此,我们开发了一种基于冷冻损伤的研究肝脏再生的新模型。为了在细胞分辨率下可视化肝脏再生,我们采用了CUBIC组织透明化方法。肝脏冷冻损伤诱导了一个局部坏死和凋亡病变,其特征为炎症和先天免疫细胞浸润。在这个初始阶段之后,我们观察到了纤维化,在30天内随着再生重新建立内环境稳态而消退。重要的是,这种方法能够在单个动物体内比较健康和受损的实质组织,比以前的模型具有独特优势。总之,肝脏冷冻损伤模型为研究纤维化和肝脏再生的细胞及分子途径提供了一种快速且可重复的方法。