Suppr超能文献

提高分离人肝细胞的冷藏效果。

Improvement of the cold storage of isolated human hepatocytes.

机构信息

Institut für Physiologische Chemie, Universitätsklinikum Essen, Essen, Germany.

出版信息

Cell Transplant. 2012;21(1):23-37. doi: 10.3727/096368911X580509. Epub 2011 Jun 7.

Abstract

Increasing amounts of human hepatocytes are needed for clinical applications and different fields of research, such as cell transplantation, bioartificial liver support, and pharmacological testing. This demand calls for adequate storage options for isolated human liver cells. As cryopreservation results in severe cryoinjury, short-term storage is currently performed at 2-8°C in preservation solutions developed for the storage of solid organs. However, besides slowing down cell metabolism, cold also induces cell injury, which is, in many cell types, iron dependent and not counteracted by current storage solutions. In this study, we aimed to characterize storage injury to human hepatocytes and develop a customized solution for cold storage of these cells. Human hepatocytes were isolated from material obtained from partial liver resections, seeded in monolayer cultures, and, after a preculture period, stored in the cold in classical and new solutions followed by rewarming in cell culture medium. Human hepatocytes displayed cold-induced injury, resulting in >80% cell death (LDH release) after 1 week of cold storage in University of Wisconsin solution or cell culture medium and 3 h of rewarming. Cold-induced injury could be significantly reduced by the addition of the iron chelators deferoxamine and LK 614. Experiments with modified solutions based on the new organ preservation solution Custodiol-N showed that ion-rich variants were better than ion-poor variants, chloride-rich solutions better than chloride-poor solutions, potassium as main cation superior to sodium, and pH 7.0 superior to pH 7.4. LDH release after 2 weeks of cold storage in the thus optimized solution was below 20%, greatly improving cold storage of human hepatocytes. The results were confirmed by the assessment of hepatocellular mitochondrial membrane potential and functional parameters (resazurin reduction, glucagon-stimulated glucose liberation) and thus suggest the use of a customized hepatocyte storage solution for the cold storage of these cells.

摘要

为了满足临床应用和细胞移植、生物人工肝脏支持、药物测试等不同研究领域的需求,需要大量的人源肝细胞。这种需求需要为分离的人源肝细胞提供充足的储存选择。由于冷冻保存会导致严重的冷冻损伤,目前在 2-8°C 的保存液中进行短期储存,这些保存液是为保存实体器官而开发的。然而,除了减缓细胞代谢外,低温还会导致细胞损伤,在许多细胞类型中,这种损伤是铁依赖性的,目前的储存液无法对抗。在这项研究中,我们旨在研究人源肝细胞的储存损伤,并开发一种用于这些细胞低温储存的定制溶液。人源肝细胞从部分肝切除获得的材料中分离出来,接种在单层培养物中,经过预培养期后,在冷环境中用经典和新溶液储存,然后在细胞培养液中复温。人源肝细胞在冷环境中会受到损伤,在威斯康星大学溶液或细胞培养液中冷储存 1 周,复温 3 小时后,细胞死亡率(LDH 释放)超过 80%。通过添加铁螯合剂去铁胺和 LK 614,可以显著减少冷诱导的损伤。基于新型器官保存液 Custodiol-N 的改良溶液实验表明,富含离子的溶液优于贫离子的溶液,富含氯离子的溶液优于贫氯离子的溶液,钾作为主要阳离子优于钠,pH7.0 优于 pH7.4。在优化后的溶液中冷储存 2 周后,LDH 释放低于 20%,大大提高了人源肝细胞的冷储存效果。这些结果通过评估肝细胞线粒体膜电位和功能参数(resazurin 还原、胰高血糖素刺激的葡萄糖释放)得到了证实,因此建议使用定制的肝细胞储存液来储存这些细胞。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验