Hepatic "stem" cells: Coming full circle

被引:48
作者
Petersen, BE [1 ]
机构
[1] Univ Florida, Coll Med, Dept Pathol Immunol & Lab Med, Stem Cell Program, Gainesville, FL 32610 USA
关键词
D O I
10.1006/bcmd.2001.0422
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Activation, proliferation, and differentiation of a distinct phenotype of cells, called oval cells, are observed after severe hepatic injuries in which the proliferation of existing hepatocytes is inhibited. Under those conditions, oval cells can act as bipotential progenitors of the two types of epithelial cells within the liver, hepatocytes and bile ductular cells. Oval cells are also believed to play a role in the hepatocellular carcinoma and cholangiocarcinoma development; although circumstantial data are available, no direct evidence exists to support this theory. Oval cells have usually been thought to be the progeny of all hepatic stem cell, native to the liver. Recently, however, we, as well as others, have obtained clear evidence that in the rodents, hepatic oval cells, or at least a fraction of them, can derive from a precursor cell of bone marrow origin. The rodent data have been supported by recent findings that human bone marrow cells are capable or becoming hepatocytes and cholangiocytes as well. Having shown that oval cells can be derived from an extrahepatic source, we now have the technology to address many unanswered questions in oval cell origin, fate, and physiology through the use of sex-mismatched bone marrow transplants. (C) 2001 Academic Press.
引用
收藏
页码:590 / 600
页数:11
相关论文
共 35 条
[11]   Synergistic effects of hepatocyte growth factor on human cord blood CD34(+) progenitor cells are the result of c-met receptor expression [J].
Goff, JP ;
Shields, DS ;
Petersen, BE ;
Zajac, VF ;
Michalopoulos, GK ;
Greenberger, JS .
STEM CELLS, 1996, 14 (05) :592-602
[12]  
Grisham J. W., 1997, P233, DOI 10.1016/B978-012563455-7/50009-X
[13]   Platelet factor 4 and other CXC chemokines support the survival of normal hematopoietic cells and reduce the chemosensitivity of cells to cytotoxic agents [J].
Han, ZC ;
Lu, M ;
Li, JM ;
Defard, M ;
Boval, B ;
Schlegel, N ;
Caen, JP .
BLOOD, 1997, 89 (07) :2328-2335
[14]  
HATCH H, 2001, UNPUB SDF1 CXCR4 POS
[15]   DIFFERENTIATION OF THE MOUSE HEPATIC PRIMORDIUM .2. EXTRINSIC ORIGIN OF THE HEMATOPOIETIC-CELL LINE [J].
HOUSSAINT, E .
CELL DIFFERENTIATION, 1981, 10 (05) :243-252
[16]  
HU ZY, 1993, AM J PATHOL, V142, P1823
[17]   A minimally toxic dose of methylene dianiline injures biliary epithelial cells in rats [J].
Kanz, MF ;
Gunasena, GH ;
Kaphalia, L ;
Hammond, DK ;
Syed, YA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1998, 150 (02) :414-426
[18]   METHYLENE DIANILINE - ACUTE TOXICITY AND EFFECTS ON BILIARY FUNCTION [J].
KANZ, MF ;
KAPHALIA, L ;
KAPHALIA, BS ;
ROMAGNOLI, E ;
ANSARI, GAS .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 117 (01) :88-97
[19]   Morphogenetic events in mixed cultures of rat hepatocytes and nonparenchymal cells maintained in biological matrices in the presence of hepatocyte growth factor and epidermal growth factor [J].
Michalopoulos, GK ;
Bowen, WC ;
Zajac, VF ;
Beer-Stolz, D ;
Watkins, S ;
Kostrubsky, V ;
Strom, SC .
HEPATOLOGY, 1999, 29 (01) :90-100
[20]   Liver regeneration [J].
Michalopoulos, GK ;
DeFrances, MC .
SCIENCE, 1997, 276 (5309) :60-66