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用于重复临床输注的肝细胞短期储存策略。

Strategies for short-term storage of hepatocytes for repeated clinical infusions.

作者信息

Jorns Carl, Gramignoli Roberto, Saliem Mohammed, Zemack Helen, Mörk Lisa-Mari, Isaksson Bengt, Nowak Greg, Ericzon Bo-Göran, Strom Stephen, Ellis Ewa

机构信息

Division of Transplantation Surgery, Department of Clinical Science, Intervention and Technology (CLINTEC), Karolinska Institute, Karolinska University Hospital Huddinge, Stockholm, Sweden.

出版信息

Cell Transplant. 2014;23(8):1009-18. doi: 10.3727/096368913X667484.

Abstract

Hepatocyte transplantation is an upcoming treatment for patients with metabolic liver diseases. Repeated cell infusions over 1-2 days improve clinical outcome. Isolated hepatocytes are usually cold stored in preservation solutions between repeated infusions. However, during cold storage isolated hepatocytes undergo cell death. We investigated if tissue preservation and repeated isolations are better than storage of isolated hepatocytes when cold preserving human hepatocytes. Liver tissue obtained from liver surgery or organ donors was divided into two pieces. Hepatocytes were isolated by collagenase digestion. Hepatocytes were analyzed directly after isolation (fresh) or after storage for 48 h at 4°C in University of Wisconsin solution (UW cells). Liver tissue from the same donor was stored at 4°C in UW and hepatocytes were isolated after 48 h (UW tissue cells). Hepatocyte viability and function was evaluated by trypan blue exclusion, plating efficiency, ammonia metabolism, CYP 1A1/2, 2C9, 3A7, and 3A4 activities, phase II conjugation, and apoptosis evaluation by TUNEL assay and caspase-3/7 activities. Hepatocytes stored in UW showed a significantly lower viability compared to fresh cells or hepatocytes isolated from tissue stored for 48 h (54% vs. 71% vs. 79%). Plating efficiency was significantly decreased for cells stored in UW (40%) compared to fresh and UW tissue cells (63% vs. 55%). No significant differences between UW cells and UW tissue cells could be shown for CYP activities or ammonia metabolism. Hepatocytes stored in UW showed a strong increase in TUNEL-positive cells, whereas TUNEL staining in cold-stored liver tissue and hepatocytes isolated after 48 h was unchanged. This observation was confirmed by increased caspase-3/7 activities in UW cells. Although preservation of isolated hepatocytes in UW maintains function, cold storage of liver tissue and repeated hepatocyte isolations is superior to cold storage of isolated hepatocytes in preserving hepatocyte viability and function.

摘要

肝细胞移植是一种用于治疗代谢性肝病患者的新兴疗法。在1 - 2天内反复进行细胞输注可改善临床疗效。在反复输注之间,分离出的肝细胞通常保存在保存液中冷藏。然而,在冷藏过程中,分离出的肝细胞会发生细胞死亡。我们研究了在冷藏保存人肝细胞时,组织保存和反复分离是否优于分离肝细胞的储存。从肝脏手术或器官供体获取的肝脏组织被分成两块。通过胶原酶消化分离肝细胞。肝细胞在分离后(新鲜状态)或在威斯康星大学溶液(UW溶液)中于4°C储存48小时后进行分析(UW细胞)。来自同一供体的肝脏组织在UW溶液中于4°C储存,48小时后分离肝细胞(UW组织细胞)。通过台盼蓝排斥试验、接种效率、氨代谢、CYP 1A1/2、2C9、3A7和3A4活性、II相结合以及通过TUNEL检测和caspase - 3/7活性评估细胞凋亡来评价肝细胞活力和功能。与新鲜细胞或从储存48小时的组织中分离出的肝细胞相比,保存在UW溶液中的肝细胞活力显著降低(分别为54%、71%和79%)。与新鲜细胞和UW组织细胞相比,保存在UW溶液中的细胞接种效率显著降低(40%)(分别为63%和55%)。在CYP活性或氨代谢方面,UW细胞和UW组织细胞之间未显示出显著差异。保存在UW溶液中的肝细胞TUNEL阳性细胞显著增加,而冷藏的肝脏组织和48小时后分离出的肝细胞中的TUNEL染色未发生变化。UW细胞中caspase - 3/7活性增加证实了这一观察结果。尽管在UW溶液中保存分离出的肝细胞可维持功能,但肝脏组织的冷藏和反复肝细胞分离在保存肝细胞活力和功能方面优于分离肝细胞冷藏。

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