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在冈恩大鼠中用稳定转导的条件永生化肝细胞进行肝脏再填充。

Hepatic repopulation with stably transduced conditionally immortalized hepatocytes in the Gunn rat.

作者信息

Kawashita Yujo, Guha Chandan, Moitra Rituparna, Wang Xia, Fox Ira J, Roy-Chowdhury Jayanta, Roy-Chowdhury Namita

机构信息

Department of Medicine, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, New York, NY 10461, USA.

出版信息

J Hepatol. 2008 Jul;49(1):99-106. doi: 10.1016/j.jhep.2008.02.020. Epub 2008 Apr 9.

Abstract

BACKGROUND/AIMS: Conditionally immortalized hepatocytes offer a renewable source of hepatocytes, but although preparative maneuvers have been developed for hepatic repopulation with primary hepatocytes, extensive proliferation of transplanted immortalized hepatocytes has not been accomplished heretofore. Our aim was to achieve ex vivo gene therapy of uridinediphosphoglucuronate glucuronosyltransferase-1A1 (UGT1A1)-deficient jaundiced Gunn rats (model of Crigler-Najjar syndrome type-1) by hepatic repopulation with genetically modified and conditionally immortalized hepatocytes.

METHODS

Gunn rat hepatocytes were conditionally immortalized by stable transduction with a thermolabile mutant simian virus 40 T-antigen ((ts)Tag(A58)) and further transduced with UGT1A1. These hepatocytes proliferate at 33 degrees C, but at 37 degrees C the (ts)Tag(A58) is degraded and the cells become quiescent. The cells were transplanted into Gunn rat livers after preparative hepatic irradiation (50 Gy) and 66% hepatectomy.

RESULTS

The engrafted UGT1A1-positive immortalized hepatocytes replaced approximately 80% of the host hepatocytes in 20 weeks, leading to normalization of hyperbilirubinemia. Liver histology, and serum albumin and alanine aminotransferase levels remained normal.

CONCLUSIONS

We achieved complete cure of hyperbilirubinemia in Gunn rats by ex vivo gene therapy via genetically modified and conditionally immortalized hepatocytes.

摘要

背景/目的:条件永生化肝细胞提供了一种可再生的肝细胞来源,但是尽管已经开发出了用原代肝细胞进行肝脏再填充的制备方法,但迄今为止,移植的永生化肝细胞尚未实现广泛增殖。我们的目的是通过用基因改造的条件永生化肝细胞进行肝脏再填充,对尿苷二磷酸葡萄糖醛酸葡萄糖醛酸基转移酶-1A1(UGT1A1)缺陷的黄疸Gunn大鼠(1型克里格勒-纳贾尔综合征模型)进行离体基因治疗。

方法

通过用热不稳定突变体猿猴病毒40 T抗原((ts)Tag(A58))进行稳定转导,使Gunn大鼠肝细胞条件永生化,并进一步用UGT1A1转导。这些肝细胞在33℃时增殖,但在37℃时(ts)Tag(A58)降解,细胞变得静止。在进行肝脏照射(50 Gy)和66%肝切除术后,将这些细胞移植到Gunn大鼠肝脏中。

结果

移植的UGT1A1阳性永生化肝细胞在20周内取代了约80%的宿主肝细胞,导致高胆红素血症正常化。肝脏组织学、血清白蛋白和丙氨酸转氨酶水平保持正常。

结论

我们通过基因改造的条件永生化肝细胞进行离体基因治疗,实现了Gunn大鼠高胆红素血症的完全治愈。

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