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来自屠宰场器官的猪肝细胞。生物人工肝装置的无限资源。

Porcine hepatocytes from slaughterhouse organs. An unlimited resource for bioartificial liver devices.

作者信息

Koebe H G, Pahernik S A, Sproede M, Thasler W E, Schildberg F W

机构信息

Department of Surgery, Klinikum Grosshadern, L.M. University of Munich, Germany.

出版信息

ASAIO J. 1995 Apr-Jun;41(2):189-93.

PMID:7640425
Abstract

Most recent strategies for the development of hybrid artificial liver devices focus on the use of parenchymal liver cells (hepatocytes). For clinical application of these devices, a sufficient cell supply is mandatory. Because human liver tissue is rarely available, isolated porcine hepatocytes from laboratory animals have been suggested for use in bioartificial livers. The authors introduce a modified isolation protocol to yield large scale numbers of viable porcine hepatocytes from slaughterhouse organs. Perfusion and enzymatic digestion of the left medial liver lobe (n = 74) resulted in 1.0 +/- 0.3 x 10(7) viable hepatocytes per gram of tissue, and an overall yield of 1.92 +/- 0.5 x 10(9) viable cells per isolation (viability: 93 +/- 2%). Collagen gel immobilization maintained morphologic integrity and functional activity of hepatocyte cultures over long-term periods. Cell morphology, as assessed by light microscopic evaluation, was maintained for 2 weeks. Stable DNA content (51 +/- 5 micrograms) and low values of alanine aminotransferase release (8 microU/hr/micrograms DNA) indicated structural stability of cultures after a short period of post isolational adaptation. Albumin secretion (4.5 micrograms/hr/micrograms DNA) and persistent Cytochrome P450 IA1 dependent deethylation of 7-ethoxycoumarin (4.5 nmol/hr/micrograms DNA) indicated long-term metabolic activity of cultured hepatocytes. Hepatocytes from livers of slaughtered pigs represent an unlimited resource of viable material for cell culture, and their usefulness as functional units of bioartificial liver support devices should be tested.

摘要

近期开发混合人工肝装置的多数策略都聚焦于实质肝细胞(肝细胞)的应用。对于这些装置的临床应用而言,充足的细胞供应必不可少。由于人类肝脏组织很少可得,因此有人建议将从实验动物中分离得到的猪肝细胞用于生物人工肝。作者介绍了一种改良的分离方案,以便从屠宰场器官中获取大量有活力的猪肝细胞。对左内侧肝叶(n = 74)进行灌注和酶消化后,每克组织可产生1.0±0.3×10⁷个有活力的肝细胞,每次分离的总产率为1.92±0.5×10⁹个有活力的细胞(活力:93±2%)。胶原凝胶固定化可长期维持肝细胞培养物的形态完整性和功能活性。通过光学显微镜评估,细胞形态可维持2周。稳定的DNA含量(51±5微克)和低水平的丙氨酸转氨酶释放(8微单位/小时/微克DNA)表明分离后经过短时间适应,培养物具有结构稳定性。白蛋白分泌(4.5微克/小时/微克DNA)以及7-乙氧基香豆素依赖细胞色素P450 IA1的持续脱乙基作用(4.5纳摩尔/小时/微克DNA)表明培养的肝细胞具有长期代谢活性。屠宰猪肝脏中的肝细胞是用于细胞培养的无限有活力材料资源,其作为生物人工肝支持装置功能单元的效用应予以测试。

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