Stem Cell Convergence Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-Ro, Yuseong-Gu, Daejeon, 34141, Republic of Korea.
Department of Functional Genomics, Korea University of Science & Technology (UST), 217 Gajungro, Yuseong-Gu, Daejeon, 34113, Republic of Korea.
Sci Rep. 2023 Dec 22;13(1):22935. doi: 10.1038/s41598-023-50250-w.
Genetic liver disease modeling is difficult because it is challenging to access patient tissue samples and to develop practical and relevant model systems. Previously, we developed novel proliferative and functional liver organoids from pluripotent stem cells; however, the protocol requires improvement for standardization and reproducible mass production. Here, we improved the method such that it is suitable for scalable expansion and relatively homogenous production, resulting in an efficient and reproducible process. Moreover, three medium components critical for long-term expansion were defined. Detailed transcriptome analysis revealed that fibroblast growth factor signaling, the essential pathway for hepatocyte proliferation during liver regeneration, was mainly enriched in proliferative liver organoids. Short hairpin RNA-mediated knockdown of FGFR4 impaired the generation and proliferation of organoids. Finally, glycogen storage disease type Ia (GSD1a) patient-specific liver organoids were efficiently and reproducibly generated using the new protocol. They well maintained disease-specific phenotypes such as higher lipid and glycogen accumulation in the liver organoids and lactate secretion into the medium consistent with the main pathologic characteristics of patients with GSD1a. Therefore, our newly established liver organoid platform can provide scalable and practical personalized disease models and help to find new therapies for incurable liver diseases including genetic liver diseases.
遗传肝脏疾病模型的建立具有一定难度,因为获取患者组织样本以及开发实用且相关的模型系统颇具挑战。先前,我们从多能干细胞中开发了新型增殖型和功能性肝脏类器官;然而,该方案需要改进,以实现标准化和可重复的大规模生产。在此,我们改进了该方法,使其适合可扩展的扩增和相对同质的生产,从而实现高效且可重复的过程。此外,还确定了三个对长期扩增至关重要的培养基成分。详细的转录组分析表明,成纤维细胞生长因子信号转导是肝再生过程中肝细胞增殖的必需途径,主要富集在增殖型肝脏类器官中。短发夹 RNA 介导的 FGFR4 敲低会损害类器官的生成和增殖。最后,使用新方案高效且可重复地生成了糖原贮积症 1a 型 (GSD1a) 患者特异性肝脏类器官。它们很好地保持了疾病特异性表型,例如肝脏类器官中更高的脂质和糖原积累,以及向培养基中分泌乳酸,这与 GSD1a 患者的主要病理特征一致。因此,我们新建立的肝脏类器官平台可以提供可扩展且实用的个性化疾病模型,并有助于为包括遗传肝脏疾病在内的不可治愈的肝脏疾病找到新的治疗方法。