Green fluorescent protein-transgenic rat: A tool for organ transplantation research

被引:154
作者
Hakamata, Y
Tahara, K
Uchida, H
Sakuma, Y
Nakamura, M
Kume, A
Murakami, T
Takahashi, M
Takahashi, R
Hirabayashi, M
Ueda, M
Miyoshi, I
Kasai, N
Kobayashi, E
机构
[1] Jichi Med Sch, Ctr Mol Med, Div Organ Replacement Res, Kawachi, Tochigi 3290498, Japan
[2] Jichi Med Sch, Ctr Mol Med, Div Anim Transgen Res, Kawachi, Tochigi 3290498, Japan
[3] Jichi Med Sch, Ctr Mol Med, Div Mol Immunol, Kawachi, Tochigi 3290498, Japan
[4] YS New Technol Inst Inc, Ishibashi, Tochigi, Japan
[5] Tohoku Univ, Sch Med, Inst Anim Experimentat, Sendai, Miyagi 980, Japan
关键词
transgenic rat; green fluorescent protein; transplantation; donor cell migration; flow cytometry;
D O I
10.1006/bbrc.2001.5452
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The purpose of this study is to evaluate green fluorescent protein (GFP) transgenic rats for use as a tool for organ transplantation research. The GFP gene construct was designed to express ubiquitously. By flow cytometry, the cells obtained from the bone marrow, spleen, and peripheral blood of the GFP transgenic rats consisted of 77, 91, and 75% GFP-positive cells, respectively. To examine cell migration of GFP-positive cells after organ transplantation, pancreas graft with or without spleen transplantation, heart graft with or without lung transplantation, auxiliary liver and small bowel transplantation were also performed from GFP transgenic rat to LEW (RT1(1)) rats under a 2-week course of 0.64 mg/kg tacrolimus administration. GFP-positive donor cells were detected in the fully allogenic LEW rats after organ transplantation. These results showed that GFP transgenic rat is a useful tool for organ transplantation research such as cell migration study after organ transplantation without donor cell staining. (C) 2001 Academic Press.
引用
收藏
页码:779 / 785
页数:7
相关论文
共 27 条
[1]   Usefulness of direct sequencing in the detection of microchimerism in liver transplant recipients [J].
Curcio, M ;
Mosca, M ;
Lapi, S ;
Filipponi, F ;
Mosca, F ;
Italia, S ;
Rizzo, G .
TRANSPLANTATION, 2000, 69 (01) :191-191
[2]   DONOR DENDRITIC CELLS AFTER LIVER AND HEART ALLOTRANSPLANTATION UNDER SHORT-TERM IMMUNOSUPPRESSION [J].
DEMETRIS, AJ ;
MURASE, N ;
STARZL, TE .
LANCET, 1992, 339 (8809) :1610-1610
[3]   THE RAT AS AN EXPERIMENTAL ANIMAL [J].
GILL, TJ ;
SMITH, GJ ;
WISSLER, RW ;
KUNZ, HW .
SCIENCE, 1989, 245 (4915) :269-276
[4]  
HIRABAYASHI M, 2001, IN PRESS TRANSGENIC
[5]   Development, stability, and clinical correlations of allogeneic microchimerism after solid organ transplantation [J].
Hisanaga, M ;
Hundrieser, J ;
Boker, E ;
Uthoff, K ;
Raddatz, G ;
Wahlers, T ;
Wonigeit, K ;
Pichlmayr, R ;
Schlitt, HJ .
TRANSPLANTATION, 1996, 61 (01) :40-45
[6]  
HOCHI S-I, 1990, Animal Biotechnology, V1, P175, DOI 10.1080/10495399009525739
[7]   'Green mice' and their potential usage is biological research [J].
Ikawa, M ;
Yamada, S ;
Nakanishi, T ;
Okabe, M .
FEBS LETTERS, 1998, 430 (1-2) :83-87
[8]  
Kawakami N, 1999, IMMUNOL LETT, V70, P165
[9]   Ubiquitous expression of marker transgenes in mice and rats [J].
Kisseberth, WC ;
Brettingen, NT ;
Lohse, JK ;
Sandgren, EP .
DEVELOPMENTAL BIOLOGY, 1999, 214 (01) :128-138
[10]   The functional relevance of passenger leukocytes and microchimerism for heart allograft acceptance in the rat [J].
Ko, S ;
Deiwick, A ;
Jäger, MD ;
Dinkel, A ;
Rohde, F ;
Fischer, R ;
Tsui, TY ;
Rittmann, KL ;
Wonigeit, K ;
Schlitt, HJ .
NATURE MEDICINE, 1999, 5 (11) :1292-1297