Identification of the indoleamine 2,3-dioxygenase nucleotide sequence in a rat liver transplant model

被引:10
作者
Pan, TL
Lin, CL
Chen, CL
Lin, YC
Gojo, S
Lee, TH
Wang, YH
Lord, R
Lai, CY
Tsu, LW
Tseng, HP
Wu, ML
Iwashita, Y
Kitano, S
Chiang, KC
Hashimoto, T
Sugioka, A
Goto, S
机构
[1] Chang Gung Mem Hosp, Dept Surg, Kaohsiung, Taiwan
[2] Saitama Med Univ, Dept Surg 1, Saitama, Japan
[3] Univ Tasmania, Discipline Surg, Hobart, Tas, Australia
[4] Oita Med Univ, Dept Surg 1, Oita, Japan
[5] Nagoya City Univ, Sch Med, Dept Surg 1, Nagoya, Aichi 467, Japan
[6] Fujita Hlth Univ, Sch Med, Dept Surg, Fujita, Japan
关键词
liver transplantation; rat; rejection; tolerance; tryptophan; indoleamine 2,3-dioxygenase; orthotopic liver transplantation (OLT); reverse transcription (RT)-PCR;
D O I
10.1016/S0966-3274(00)00024-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A tryptophan catabolizer, indoleamine 2,3-dioxygenase (IDO) is highly expressed in the placenta and plays an essential role in maternal tolerance. Recent data have shown that the administration of an IDO inhibitor blocked not only maternal tolerance but also liver allograft tolerance. However, little is known about the induction of IDO in liver allografts, although a gene specific for tryptophan 2,3-dioxygenase (TDO) is believed to be expressed in the liver. In the present study, we investigated whether IDO is induced in liver allografts. Synthetic oligonucleotide primers based on the mouse IDO cDNA sequence were used to amplify RNA derived from livers of donor, syngeneic or allogeneic OLT rats. RNA encoding IDO was induced in the rat allogeneic liver after orthotopic liver transplantation (OLT), but not in syngeneic OLT. The rat nucleotide sequence of the RT-PCR products obtained from OLT livers revealed identities of 89% homology to the mouse IDO and of 68% to the human IDO. This study demonstrated the presence of RNA encoding IDO in allogeneic OLT livers, which may be involved in the immune response after liver transplantation. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 194
页数:6
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