Changes in liver regenerative factors in a case of living-related liver transplantation

被引:15
作者
Eguchi, S [1 ]
Okudaira, S [1 ]
Azuma, T [1 ]
Ohno, Y [1 ]
Fujioka, H [1 ]
Furui, J [1 ]
Tanaka, K [1 ]
Kanematsu, T [1 ]
机构
[1] Nagasaki Univ, Sch Med, Dept Surg 2, Nagasaki 8528501, Japan
关键词
fulminant hepatic failure; hepatocyte growth factor; liver regeneration; living-related liver transplantation;
D O I
10.1034/j.1399-0012.1999.130616.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Liver regeneration in a patient with fulminant hepatic failure (FHF) who underwent living-related partial liver transplantation (LRLT) was investigated regarding hepatic growth factors. The patient was a 16-yr-old Japanese male who developed severe subacute FHF. LRLT was performed using an extended left lobe of the ABO matched patient's mother. In the recipient, the pre-transplant levels of both plasma hepatocyte growth factor (HGF) and transforming growth factor (TGF)-beta were extremely high and rapidly decreased following the liver replacement. The liver volume evaluated using a CAT scan increased 195% after 2 wk in graft liver and 110% after 2 wk in the hepatectomized donor. The explanted liver (FHF river), the river from donor (normal liver), and the graft liver [the 3rd post-transplant day (POD 3)] were all investigated immunohistochemically. FHF liver: No liver regeneration was observed [proliferative cell nuclear antigen (PCNA) labeling index (L.I.): 0%]. In the liver, both HGF in the hepatocytes and c-met on the membrane of the hepatocytes were positive. TGF-beta was positive in the hepatocytes and no apoptosis was detected by the TUNEL method. Donor liver (POD 0): Few PCNA stained hepatocytes were detected. No HGF was detected but c-met was clearly detected on the cell membrane of the hepatocytes. Neither TGF-beta nor apoptosis was detected. Graft liver (POD 3): The PCNA L.I. was conspicuous at 40%. HGF was positive in non-parenchymal cells and c-met was positive in the cytoplasm of the hepatocytes. TGF-beta was negative while apoptosis was positive in the zone 3 hepatocytes. In conclusion, these findings suggested that the liver of the patient with FHF did not respond to liver regenerative stimulus, in part, through involvement of inhibitor TGF-beta. On POD 3, the transplanted graft was in a vigorous regenerative status in comparison to that in the hepatectomized donor. The HGF/c-met system is thought to be involved in the mechanism of regeneration. Intrahepatic apoptosis was detected in the graft on the 3rd post-transplant day probably due to transient ischemia in the liver, which was not related to the Fas/Fas-ligand system.
引用
收藏
页码:536 / 544
页数:9
相关论文
共 35 条
[1]
ARMENDARIZBORUNDA J, 1993, LAB INVEST, V69, P283
[2]
TRANSFORMING GROWTH FACTOR-BETA MESSENGER-RNA INCREASES DURING LIVER-REGENERATION - A POSSIBLE PARACRINE MECHANISM OF GROWTH-REGULATION [J].
BRAUN, L ;
MEAD, JE ;
PANZICA, M ;
MIKUMO, R ;
BELL, GI ;
FAUSTO, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1539-1543
[3]
Chari R S, 1996, Liver Transpl Surg, V2, P233, DOI 10.1002/lt.500020309
[4]
CHUNG ML, 1996, TRANSPLANTATION, V62, P696
[5]
Liver regeneration .3. Regulation of signal transduction during liver regeneration [J].
Diehl, AM ;
Rai, RM .
FASEB JOURNAL, 1996, 10 (02) :215-227
[6]
Loss and recovery of liver regeneration in rats with fulminant hepatic failure [J].
Eguchi, S ;
Lilja, H ;
Hewitt, WR ;
Middleton, Y ;
Demetriou, AA ;
Rozga, J .
JOURNAL OF SURGICAL RESEARCH, 1997, 72 (02) :112-122
[7]
Eguchi S, 1996, HEPATOLOGY, V24, P1452
[8]
The Fas/Fas-ligand system functions in hepatocytes in the early stage of fulminant hepatic failure in rats [J].
Eguchi, S ;
Matsuzaki, S ;
Fujioka, H ;
Koji, T ;
Higami, Y ;
Kanematsu, T .
HEPATOLOGY RESEARCH, 1998, 11 (02) :103-114
[9]
FRANCAVILLA A, 1994, HEPATOLOGY, V19, P210
[10]
STIMULATION OF LIVER GROWTH BY EXOGENOUS HUMAN HEPATOCYTE GROWTH-FACTOR IN NORMAL AND PARTIALLY HEPATECTOMIZED RATS [J].
FUJIWARA, K ;
NAGOSHI, S ;
OHNO, A ;
HIRATA, K ;
OHTA, Y ;
MOCHIDA, S ;
TOMIYA, T ;
HIGASHIO, K ;
KUROKAWA, K .
HEPATOLOGY, 1993, 18 (06) :1443-1449