Steatotic liver transplantation in the mouse: A model of primary nonfunction

被引:16
作者
Birsner, JH
Wan, CD
Cheng, G
Evans, ZP
Polito, CC
Fiorini, RN
Gilbert, G
Haines, JK
Schmidt, MG
Chavin, KD
机构
[1] Med Univ S Carolina, Dept Surg, Div Transplantat, Charleston, SC 29425 USA
[2] Med Univ S Carolina, Dept Microbiol & Immunol, Charleston, SC 29425 USA
关键词
ob/ob; ischemia/reperfusion; hepatocyte; animal; nonarterialized;
D O I
10.1016/j.jss.2003.11.022
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. The number of potential donor organs deemed suboptimal for transplantation because of hepatic steatosis is rising as the obesity rate increases. However, no mouse transplant model has been described within the framework of hepatic steatosis. We describe the development of and our initial experience with a steatotic mouse orthotopic liver transplant model using the ob/ob mouse. This model is technically achievable and functionally mimics primary nonfunction. Materials and methods. Adapting techniques of a nonarterialized murine transplant model, C57BL6 ob/ob mice aged 5-7 weeks (26-35 g) and lean controls served as liver donors and recipients. Orthotopic liver transplantation (OLT) was performed using a two-cuff technique at the infrahepatic cava and portal vein. The suprahepatic cava was anastomosed end to end, and the bile duct was stented. The hepatic artery was not reconstructed. Results. Lean-to-lean OLT was performed with 70% (n = 10) long-term survival. ob/ob-to-age-matched lean recipients had 0% (n = 10) survival because of size discrepancy. ob/ob livers were transplanted to size-matched lean recipients ( > 3 months old) with short-term survival of 30% (n = 10). These mice survived the operation, awakened, but expired within 24 h. Serum transaminases revealed a significantly higher injury profile in the recipients of the steatotic livers, and histology showed massive centrilobular coagulative necrosis with hemorrhage, the overall picture being that of primary nonfunction. Conclusions. This novel use of the ob/ob mouse for OLT provides us with a model for steatotic transplantation with primary nonfunction as the end point and may help to better understand the response of the steatotic liver to the insult of transplantation. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:97 / 101
页数:5
相关论文
共 12 条
[1]   Disruption of leptin signaling contributes to cardiac hypertrophy independently of body weight in mice [J].
Barouch, LA ;
Berkowitz, DE ;
Harrison, RW ;
O'Donnell, CP ;
Hare, JM .
CIRCULATION, 2003, 108 (06) :754-759
[2]   Leptin and clinical medicine: A new piece in the puzzle of obesity [J].
Bray, GA ;
York, DA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (09) :2771-2776
[3]   Orthotopic liver transplantation in knockout mice:: Is TNFα involved in early graft injury and regeneration? [J].
Conzelmann, LO ;
Schemmer, P ;
Zhong, Z ;
Smutney, OM ;
Bunzendahl, H ;
Thurman, RG .
TRANSPLANTATION PROCEEDINGS, 2002, 34 (06) :2299-2300
[4]   PATTERNS OF INFLAMMATORY VASCULAR ENDOTHELIAL CHANGES IN MURINE LIVER GRAFTS [J].
DAHMEN, U ;
BERGESE, SD ;
QIAN, SG ;
PELLETIER, RP ;
WU, H ;
SEDMAK, DD ;
FUNG, JJ ;
OROSZ, CG .
TRANSPLANTATION, 1995, 60 (06) :577-584
[5]   THE PREDICTIVE VALUE OF DONOR LIVER BIOPSIES FOR THE DEVELOPMENT OF PRIMARY NONFUNCTION AFTER ORTHOTOPIC LIVER-TRANSPLANTATION [J].
DALESSANDRO, AM ;
KALAYOGLU, M ;
SOLLINGER, HW ;
HOFFMANN, RM ;
REED, A ;
KNECHTLE, SJ ;
PIRSCH, JD ;
HAFEZ, GR ;
LORENTZEN, D ;
BELZER, FO .
TRANSPLANTATION, 1991, 51 (01) :157-163
[6]   Second-set rejection of mouse liver allografts is dependent on radiation-sensitive nonparenchymal cells of graft bone marrow origin [J].
Fu, FM ;
Thai, NL ;
Li, YP ;
Lu, LN ;
Thomson, AW ;
Fung, JJ ;
Qian, SG .
TRANSPLANTATION, 1996, 61 (08) :1228-1233
[7]   ORTHOTOPIC LIVER-TRANSPLANTATION IN THE RAT - TECHNIQUE USING CUFF FOR PORTAL-VEIN ANASTOMOSIS AND BILIARY DRAINAGE [J].
KAMADA, N ;
CALNE, RY .
TRANSPLANTATION, 1979, 28 (01) :47-50
[8]   IL-12 antagonism enhances apoptotic death of T cells within hepatic allografts from Flt3 ligand-treated donors and promotes graft acceptance [J].
Li, W ;
Lu, L ;
Wang, ZL ;
Wang, LF ;
Fung, JJ ;
Thomson, AW ;
Qian, SG .
JOURNAL OF IMMUNOLOGY, 2001, 166 (09) :5619-5628
[9]   Impact of donor MHC class I or class II antigen deficiency on first- and second-set rejection of mouse heart or liver allografts [J].
Qian, S ;
Fu, F ;
Li, Y ;
Lu, L ;
Rao, AS ;
Starzl, TE ;
Thomson, AW ;
Fung, JJ .
IMMUNOLOGY, 1996, 88 (01) :124-129
[10]   Hepatocyte-induced apoptosis of activated T cells, a mechanism of liver transplant tolerance, is related to the expression of ICAM-1 and hepatic lectin [J].
Qian, S ;
Wang, Z ;
Lee, Y ;
Chiang, Y ;
Bonham, C ;
Fung, J ;
Lu, L .
TRANSPLANTATION PROCEEDINGS, 2001, 33 (1-2) :226-226