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低温保存后大鼠肝细胞的活力及原代培养:Leibovitz培养基在冷藏方面优于威斯康星大学溶液。

Viability and primary culture of rat hepatocytes after hypothermic preservation: the superiority of the Leibovitz medium over the University of Wisconsin solution for cold storage.

作者信息

Poullain M G, Fautrel A, Guyomard C, Chesne C, Grislain L, Guillouzo A

机构信息

INSERM U 49, Hôpital Pontchaillou, Rennes, France.

出版信息

Hepatology. 1992 Jan;15(1):97-106. doi: 10.1002/hep.1840150118.

Abstract

Hepatocytes isolated from adult rat livers were hypothermically preserved for 24 or 48 hr before being plated under conventional culture conditions. They were stored either in the Leibovitz medium, a cell culture medium with and without polyethylene glycol (PEG), a compound known to suppress ischemia-induced cell swelling, or in the University of Wisconsin solution, the most effective solution for cold organ preservation. After 24 or 48 hr of storage at 4.5 degrees C in Leibovitz medium, cell viability and adherence efficiency to plastic dish, were only slightly reduced, whereas University of Wisconsin hepatocytes had a decreased viability and (especially after 48-hr storage) lost their adhesion ability; they did not survive in vitro. The metabolic competence of hepatocytes maintained in Leibovitz medium was retained over the 3 days of culture, as shown by low extracellular levels of the membrane-bound and cytosolic hepatic enzymes, as well as by intracellular glutathione content, albumin secretion rate and several phase I and phase II drug metabolic reactions very close to those found with fresh hepatocytes maintained under similar culture conditions. Addition of polyethylene glycol to the Leibovitz medium resulted in slightly higher viability and function of hepatocytes after cold storage. These results clearly demonstrate that viability of a transplanted liver does not correlate with long-term in vitro viability of isolated hepatocytes after hypothermic preservation in University of Wisconsin solution. They also suggest that nutritional and energy substrates as found in the Leibovitz medium are probably required to define a suitable solution for cold preservation of isolated parenchymal cells. The findings with Leibovitz medium favor the conclusion that hypothermically preserved hepatocytes could be used for various metabolic studies and for the treatment of liver insufficiency.

摘要

从成年大鼠肝脏分离出的肝细胞在常规培养条件下接种前,先进行了24或48小时的低温保存。它们被保存在莱博维茨培养基中,该培养基是一种含有或不含有聚乙二醇(PEG)的细胞培养基,聚乙二醇是一种已知可抑制缺血诱导的细胞肿胀的化合物,或者保存在威斯康星大学溶液中,这是用于冷器官保存的最有效溶液。在4.5摄氏度下于莱博维茨培养基中保存24或48小时后,细胞活力和对塑料培养皿的贴壁效率仅略有降低,而威斯康星大学溶液保存的肝细胞活力下降,并且(尤其是在保存48小时后)失去了黏附能力;它们在体外无法存活。如膜结合和胞质肝酶的细胞外水平较低以及细胞内谷胱甘肽含量、白蛋白分泌率和几种I相和II相药物代谢反应所示,在莱博维茨培养基中保存的肝细胞的代谢能力在培养的3天内得以保留,这些反应与在类似培养条件下新鲜肝细胞的反应非常接近。向莱博维茨培养基中添加聚乙二醇会使低温保存后的肝细胞活力和功能略高。这些结果清楚地表明,移植肝脏的活力与在威斯康星大学溶液中低温保存后分离的肝细胞的长期体外活力无关。它们还表明,莱博维茨培养基中发现的营养和能量底物可能是确定分离的实质细胞冷保存合适溶液所必需的。莱博维茨培养基的研究结果支持这样的结论,即低温保存的肝细胞可用于各种代谢研究和治疗肝功能不全。

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