Hepatic oval 'stem' cell in liver regeneration

被引:114
作者
Oh, SH [1 ]
Hatch, HM [1 ]
Petersen, BE [1 ]
机构
[1] Univ Florida, Coll Med, Dept Pathol Immunol & Lab Med, Gainesville, FL 32610 USA
关键词
regeneration; proliferation; differentiation;
D O I
10.1016/S1084952102001271
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Hepatic oval cell activation, proliferation, and differentiation has been observed under certain physiological conditions, mainly when the proliferation of existing hepatocytes has been inhibited followed by severe hepatic injury. Hepatic oval cells display a distinct phenotype and have been shown to be a bipotential progenitor of two types of epithelial cells found in the liver, hepatocytes and bile ductular cells. Bone marrow stem cells have recently been shown to be a potential source of the hepatic oval cells and that reconstitution of an injured liver from a purified stem cell population is possible. The focus of this review is on the studies involving the activation, proliferation, and differentiation of these hepatic oval cells and the role that they play in regeneration of the damaged liver. In order to present the potentiality of the hepatic oval cell, an experimental model that involves the inhibition Of normal hepatic growth and division as well as severe hepatic injury via chemical or surgical means has been employed. In this model, an as yet undetermined signal or perhaps the lack of regenerative capability in the hepatocytes activates the hepatic oval cell compartment. However, other than understanding a potential origin of these cells and some of the markers that characterize them, it still remains unclear as to how these cells migrate (home) into the damaged areas and how they begin their differentiation into mature and functioning hepatic cells.
引用
收藏
页码:405 / 409
页数:5
相关论文
共 62 条
[41]  
Petersen BE, 2001, FASEB J, V15, pA1084
[42]  
Pierelli L, 2000, BLOOD, V95, P3001
[43]   INDUCTION OF LIVER GROWTH IN NORMAL MICE BY INFUSION OF HEPATOCYTE GROWTH-FACTOR SCATTER FACTOR [J].
ROOS, F ;
RYAN, AM ;
CHAMOW, SM ;
BENNETT, GL ;
SCHWALL, RH .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1995, 268 (02) :G380-G386
[44]   HEPATOCYTE GROWTH-FACTOR SCATTER FACTOR AND ITS RECEPTOR, THE C-MET PROTOONCOGENE PRODUCT [J].
RUBIN, JS ;
BOTTARO, DP ;
AARONSON, SA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1155 (03) :357-371
[45]   PARTIAL CHARACTERIZATION OF A HEPATOCYTE GROWTH-FACTOR FROM RAT PLATELETS [J].
RUSSELL, WE ;
MCGOWAN, JA ;
BUCHER, NLR .
JOURNAL OF CELLULAR PHYSIOLOGY, 1984, 119 (02) :183-192
[46]   SCATTER FACTOR/HEPATOCYTE GROWTH-FACTOR IS ESSENTIAL FOR LIVER DEVELOPMENT [J].
SCHMIDT, C ;
BLADT, F ;
GOEDECKE, S ;
BRINKMANN, V ;
ZSCHIESCHE, W ;
SHARPE, M ;
GHERARDI, E ;
BIRCHMEIER, C .
NATURE, 1995, 373 (6516) :699-702
[47]   REQUIREMENT OF TRANSCRIPTION FACTOR PU.1 IN THE DEVELOPMENT OF MULTIPLE HEMATOPOIETIC LINEAGES [J].
SCOTT, EW ;
SIMON, MC ;
ANASTASI, J ;
SINGH, H .
SCIENCE, 1994, 265 (5178) :1573-1577
[48]   HEPATOTROPIN MESSENGER-RNA EXPRESSION IN HUMAN FETAL LIVER DEVELOPMENT AND IN LIVER-REGENERATION [J].
SELDEN, C ;
JONES, M ;
WADE, D ;
HODGSON, H .
FEBS LETTERS, 1990, 270 (1-2) :81-84
[49]  
SELL S, 1990, CANCER RES, V50, P3811
[50]   THE LIVER AS A STEM-CELL AND LINEAGE SYSTEM [J].
SIGAL, SH ;
BRILL, S ;
FIORINO, AS ;
REID, LM .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (02) :G139-G148