Reproducible, Scale-Up Production of Human Liver Organoids (HLOs) on a Pillar Plate Platform via Microarray 3D Bioprinting.

Q4 Biochemistry, Genetics and Molecular Biology Methods in molecular biology Pub Date : 2025-01-17 DOI:10.1007/7651_2024_603
Sunil Shrestha, Manav Goud Vanga, Charishma Jonnadula, Prabha Acharya, Minseong Lee, Moo-Yeal Lee
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Abstract

Human liver organoids (HLOs) derived from pluripotent stem cells hold potential for disease modeling and high-throughput compound screening due to their architectural and functional resemblance to human liver tissues. However, reproducible, scale-up production of HLOs for high-throughput screening (HTS) presents challenges. These include the high costs of additives and growth factors required for cell differentiation, variability in organoid size and function from batch to batch, suboptimal maturity of HLOs compared to primary hepatocytes, and low assay throughput due to excessive manual processes and the absence of assay-ready plates with HLOs. To address some of these issues, here we present standard operating procedures (SOPs) for the scale-up production of HLOs using a pillar plate through microarray 3D bioprinting. This technology facilitates the rapid, uniform seeding of foregut cells onto the pillar plate, maintaining cell viability and enabling the scale-up generation of HLOs. The assay-ready pillar plate with HLOs is suitable for compound testing, as well as in situ organoid staining and analysis.

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通过微阵列3D生物打印技术在柱板平台上可重复、大规模生产人类肝脏类器官(HLOs)。
人类肝脏类器官(HLOs)来源于多能干细胞,由于其结构和功能与人类肝脏组织相似,因此具有疾病建模和高通量化合物筛选的潜力。然而,用于高通量筛选(HTS)的HLOs的可重复性、规模化生产存在挑战。这些因素包括细胞分化所需的添加剂和生长因子的高成本,不同批次的类器官大小和功能的可变性,与原代肝细胞相比,HLOs的成熟度不理想,以及由于过度的人工处理和缺乏HLOs的检测准备板而导致的低检测吞吐量。为了解决其中的一些问题,我们提出了通过微阵列3D生物打印柱板大规模生产HLOs的标准操作程序(sop)。该技术有助于快速、均匀地将前肠细胞播种到柱板上,保持细胞活力,并实现HLOs的规模化生产。HLOs柱板适用于化合物检测,以及原位类器官染色和分析。
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来源期刊
Methods in molecular biology
Methods in molecular biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
2.00
自引率
0.00%
发文量
3536
期刊介绍: For over 20 years, biological scientists have come to rely on the research protocols and methodologies in the critically acclaimed Methods in Molecular Biology series. The series was the first to introduce the step-by-step protocols approach that has become the standard in all biomedical protocol publishing. Each protocol is provided in readily-reproducible step-by-step fashion, opening with an introductory overview, a list of the materials and reagents needed to complete the experiment, and followed by a detailed procedure that is supported with a helpful notes section offering tips and tricks of the trade as well as troubleshooting advice.
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