Infection Biology Program and Department of Cancer Biology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio.
Cleveland Clinic College of Medicine at Case Western Reserve University, Cleveland, Ohio.
Curr Protoc. 2022 Jan;2(1):e345. doi: 10.1002/cpz1.345.
Human pluripotent stem cell (hPSC)-derived hepatocyte-like cells (HLCs) are valuable tools to study liver biology. HLCs, however, lack certain key in vivo characteristics relevant to their physiological function. One such characteristic is cellular polarity, which is critical to hepatocyte counter-current flow systems involving canalicular bile secretion and sinusoidal secretion of large quantities of serum proteins into blood. Model systems using non-polarized hepatocytes, therefore, cannot recapitulate this physiological function of hepatocytes. Here, we describe a stepwise protocol to generate hPSC-derived polarized HLCs (pol-HLCs), which feature clearly defined basolateral and apical membranes separated by tight junctions. Pol-HLCs not only display many hepatic functions but are also capable of directional cargo secretion, mimicking the counter-current flow systems. We describe protocols for stem cell culture maintenance and for differentiating hPSCs into pol-HLCs. In addition, we describe protocols to assay the pol-HLCs for basic hepatic functions and polarized hepatic characteristics. Once successfully differentiated, these pol-HLCs can be used as an in vitro model system to study hepatocyte biology, disease mechanisms, genetic variation, and drug metabolism. The establishment of hepatic polarity from non-polarized hPSCs also provides a useful tool to study the development and maintenance of hepatic polarity. © 2022 Wiley Periodicals LLC. Basic Protocol 1: Maintenance of hPSCs Basic Protocol 2: Differentiation of hPSCs to pol-HLCs Basic Protocol 3: Assaying pol-HLCs for basic hepatic functions Support Protocol 1: Assessment of pol-HLC monolayer tightness Support Protocol 2: Assessment of pol-HLC polarity.
人多能干细胞(hPSC)衍生的肝细胞样细胞(HLC)是研究肝脏生物学的有价值的工具。然而,HLC 缺乏某些与其生理功能相关的关键体内特征。其中一个特征是细胞极性,这对于涉及胆小管胆汁分泌和大量血清蛋白从窦状隙分泌到血液中的肝细胞逆流系统至关重要。因此,使用非极化肝细胞的模型系统无法再现肝细胞的这种生理功能。在这里,我们描述了一个逐步方案,用于生成 hPSC 衍生的极化 HLC(pol-HLC),其特征是具有由紧密连接分隔的明确的基底外侧和顶膜。Pol-HLC 不仅显示出许多肝脏功能,而且还能够进行定向货物分泌,模拟逆流系统。我们描述了干细胞培养维持和将 hPSC 分化为 pol-HLC 的方案。此外,我们还描述了用于测定 pol-HLC 的基本肝脏功能和极化肝脏特征的方案。一旦成功分化,这些 pol-HLC 可以用作体外模型系统来研究肝细胞生物学、疾病机制、遗传变异和药物代谢。从非极化 hPSC 建立肝极性也为研究肝极性的发育和维持提供了有用的工具。©2022 年威利父子公司。基本方案 1:hPSC 的维持基本方案 2:hPSC 分化为 pol-HLC 基本方案 3:测定 pol-HLC 的基本肝脏功能支持方案 1:pol-HLC 单层紧密性的评估支持方案 2:pol-HLC 极性的评估。