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哺乳动物肝细胞作为治疗人类肝衰竭的基础。

Mammalian hepatocytes as a foundation for treatment in human liver failure.

作者信息

Jauregui H O, Gann K L

机构信息

Department of Pathology, Rhode Island Hospital, Providence 02903.

出版信息

J Cell Biochem. 1991 Apr;45(4):359-65. doi: 10.1002/jcb.240450409.

DOI:10.1002/jcb.240450409
PMID:1646208
Abstract

Technological advances in the separation and culture of mammalian hepatocytes have facilitated the use of these cells as the foundation for either hepatocyte transplantation or hepatocyte-seeded hollow fiber liver assist devices (LAD). To fully appreciate the practical applications of these tissue engineering solutions, it is necessary to understand the types of human liver failure as well as the corresponding animal models. The most immediate application of this type of technology is the treatment of hepatic encephalopathy (HE), an acute and highly fatal complication of fulminant hepatic failure. Although the pathogenesis of HE is unknown, failure of the detoxification function of the liver is accepted as playing an important role in this disorder. Consequently, the assaying and preservation of P450 activity in the grafted cells or in the LAD must be among the main targets of this research. This review explores the problems in hepatocyte transplantation and culture that deserve special consideration and emphasizes the conditions contributing to the in vitro maintenance of phenotypic expression of these cells.

摘要

哺乳动物肝细胞分离和培养技术的进步促进了这些细胞的应用,使其成为肝细胞移植或肝细胞接种中空纤维肝辅助装置(LAD)的基础。为了充分理解这些组织工程解决方案的实际应用,有必要了解人类肝衰竭的类型以及相应的动物模型。这类技术最直接的应用是治疗肝性脑病(HE),这是暴发性肝衰竭的一种急性且高度致命的并发症。尽管HE的发病机制尚不清楚,但肝脏解毒功能的衰竭被认为在这种疾病中起重要作用。因此,检测和保存移植细胞或LAD中细胞色素P450的活性必定是本研究的主要目标之一。本综述探讨了肝细胞移植和培养中值得特别关注的问题,并强调了有助于这些细胞在体外维持表型表达的条件。

相似文献

1
Mammalian hepatocytes as a foundation for treatment in human liver failure.哺乳动物肝细胞作为治疗人类肝衰竭的基础。
J Cell Biochem. 1991 Apr;45(4):359-65. doi: 10.1002/jcb.240450409.
2
In vivo evaluation of a hollow fiber liver assist device.中空纤维型肝辅助装置的体内评估
Hepatology. 1995 Feb;21(2):460-9.
3
Hepatocyte transplantation for the treatment of human disease.肝细胞移植用于人类疾病的治疗。
Semin Liver Dis. 1999;19(1):39-48. doi: 10.1055/s-2007-1007096.
4
[Transplantation of isolated hepatocytes, is it an alternative for total liver transplantation? On the treatment of hereditary hepatic metabolic diseases].
J Chir (Paris). 2001 Dec;138(6):342-6.
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Hepatocyte transplantation into the lung for treatment of acute hepatic failure in the rat.将肝细胞移植到大鼠肺中用于治疗急性肝衰竭
Transplant Proc. 1991 Feb;23(1 Pt 1):892-3.
6
Human hepatocyte transplantation: state of the art.人肝细胞移植:现状
J Intern Med. 2009 Oct;266(4):339-57. doi: 10.1111/j.1365-2796.2009.02152.x.
7
Mechanisms of cell engraftment during liver repopulation with hepatocyte transplantation.肝细胞移植实现肝脏再填充过程中的细胞植入机制。
Semin Liver Dis. 1999;19(1):15-26. doi: 10.1055/s-2007-1007094.
8
Immunologic response to liver cell allografts.对肝细胞同种异体移植的免疫反应。
Am Surg. 1982 Jan;48(1):28-31.
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Present status and perspectives of cell-based therapies for liver diseases.基于细胞的肝脏疾病治疗方法的现状与展望
J Hepatol. 2006 Jul;45(1):144-59. doi: 10.1016/j.jhep.2006.04.002. Epub 2006 Apr 27.
10
Review of hepatocyte transplantation.肝细胞移植综述。
J Hepatobiliary Pancreat Surg. 2009;16(2):97-100. doi: 10.1007/s00534-008-0023-0. Epub 2008 Dec 27.

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Sci Rep. 2013;3:2735. doi: 10.1038/srep02735.
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The effect of hydrostatic pressure on three-dimensional chondroinduction of human adipose-derived stem cells.流体静压对人脂肪来源干细胞三维软骨诱导的影响。
Tissue Eng Part A. 2009 Oct;15(10):2937-45. doi: 10.1089/ten.TEA.2008.0672.
3
Culturing of primary hepatocytes as entrapped aggregates in a packed bed bioreactor: a potential bioartificial liver.
在填充床生物反应器中将原代肝细胞培养为包埋聚集体:一种潜在的生物人工肝。
In Vitro Cell Dev Biol. 1993 Mar;29A(3 Pt 1):249-54. doi: 10.1007/BF02634192.
4
Primary hepatocytes outperform Hep G2 cells as the source of biotransformation functions in a bioartificial liver.在生物人工肝中,原代肝细胞作为生物转化功能的来源比Hep G2细胞表现更优。
Ann Surg. 1994 Jul;220(1):59-67.
5
Extended liver-specific functions of porcine hepatocyte spheroids entrapped in collagen gel.包埋于胶原凝胶中的猪肝细胞球状体的扩展肝脏特异性功能。
In Vitro Cell Dev Biol Anim. 1995 May;31(5):340-6. doi: 10.1007/BF02634282.