Funfak Anette, Bouzhir Latifa, Gontran Emilie, Minier Nicolas, Dupuis-Williams Pascale, Gobaa Samy
Institut Pasteur, Biomaterials and Microfluidics Core Facility, Paris, France.
Université Paris-Saclay, UMR-S1174 INSERM, Orsay, France.
Front Bioeng Biotechnol. 2019 Dec 13;7:417. doi: 10.3389/fbioe.2019.00417. eCollection 2019.
The integration of bile duct epithelial cells (cholangiocytes) in artificial liver culture systems is important in order to generate more physiologically relevant liver models. Understanding the role of the cellular microenvironment on differentiation, physiology, and organogenesis of cholangiocytes into functional biliary tubes is essential for the development of new liver therapies, notably in the field of cholangiophaties. In this study, we investigated the role of natural or synthetic scaffolds on cholangiocytes cyst growth, lumen formation and polarization. We demonstrated that cholangiocyte cyst formation efficiency can be similar between natural and synthetic matrices provided that the mechanical properties of the hydrogels are matched. When using synthetic matrices, we also tried to understand the impact of elasticity, matrix metalloprotease-mediated degradation and integrin ligand density on cyst morphogenesis. We demonstrated that hydrogel stiffness regulates cyst formation. We found that controlling integrin ligand density was key in the establishment of large polarized cysts of cholangiocytes. The mechanism of lumen formation was found to rely on cell self-organization and proliferation. The formed cholangiocyte organoids showed a good MDR1 (multi drug resistance protein) transport activity. Our study highlights the advantages of fully synthetic scaffold as a tool to develop bile duct models.
在人工肝培养系统中整合胆管上皮细胞(胆管细胞)对于生成更具生理相关性的肝脏模型很重要。了解细胞微环境对胆管细胞分化、生理学以及胆管细胞向功能性胆管的器官发生的作用,对于开发新的肝脏治疗方法至关重要,尤其是在胆管疾病领域。在本研究中,我们研究了天然或合成支架对胆管细胞囊肿生长、管腔形成和极化的作用。我们证明,只要水凝胶的机械性能相匹配,天然和合成基质之间胆管细胞囊肿形成效率可能相似。使用合成基质时,我们还试图了解弹性、基质金属蛋白酶介导的降解和整合素配体密度对囊肿形态发生的影响。我们证明水凝胶硬度调节囊肿形成。我们发现控制整合素配体密度是形成大的极化胆管细胞囊肿的关键。发现管腔形成机制依赖于细胞自组织和增殖。形成的胆管细胞类器官显示出良好的多药耐药蛋白1(MDR1)转运活性。我们的研究突出了全合成支架作为开发胆管模型工具的优势。