Department of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN 55905, USA.
Department of Biomedical Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cells. 2023 Aug 1;12(15):1982. doi: 10.3390/cells12151982.
Human pluripotent stem cells (hPSCs) are capable of unlimited proliferation and can undergo differentiation to give rise to cells and tissues of the three primary germ layers. While directing lineage selection of hPSCs has been an active area of research, improving the efficiency of differentiation remains an important objective. In this study, we describe a two-compartment microfluidic device for co-cultivation of adult human hepatocytes and stem cells. Both cell types were cultured in a 3D or spheroid format. Adult hepatocytes remained highly functional in the microfluidic device over the course of 4 weeks and served as a source of instructive paracrine cues to drive hepatic differentiation of stem cells cultured in the neighboring compartment. The differentiation of stem cells was more pronounced in microfluidic co-cultures compared to a standard hepatic differentiation protocol. In addition to improving stem cell differentiation outcomes, the microfluidic co-culture system described here may be used for parsing signals and mechanisms controlling hepatic cell fate.
人多能干细胞(hPSCs)具有无限增殖的能力,并能分化为三个胚层的细胞和组织。虽然定向选择 hPSCs 的谱系分化一直是一个活跃的研究领域,但提高分化效率仍然是一个重要目标。在这项研究中,我们描述了一种用于成人人类肝细胞和干细胞共培养的两室微流控装置。两种细胞类型都以 3D 或球体形式培养。在 4 周的时间里,成年肝细胞在微流控装置中保持高度功能,并作为邻近隔室中培养的干细胞向肝分化的教学旁分泌信号的来源。与标准的肝分化方案相比,干细胞在微流控共培养中的分化更为明显。除了改善干细胞分化结果外,这里描述的微流控共培养系统还可用于解析控制肝细胞命运的信号和机制。