Phosphorylation of hepatocyte growth factor receptor and epidermal growth factor receptor of human hepatocytes can be maintained in a (3D) collagen sandwich culture system

被引:14
作者
Engl, T
Boost, KA
Leckel, K
Beecken, WD
Jonas, D
Oppermann, E
Auth, MKH
Schaudt, A
Bechstein, WO
Blaheta, RA
机构
[1] Goethe Univ Frankfurt, Univ Klin, Klin Urol & Kinderurol, Zentrum Chirurg, D-60590 Frankfurt, Germany
[2] Goethe Univ Frankfurt, Klin Allgemein & Gefasschirurg, Zentrum Chirurg, Frankfurt, Germany
[3] Univ Klinikum, Zentrum Kinderheilkunde, Essen, Germany
关键词
human hepatocytes; drug toxicity; cell architecture;
D O I
10.1016/j.tiv.2004.01.010
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In vitro culture models that employ human liver cells could be potent tools for predictive studies on drug toxicity and metabolism in the pharmaceutical industry. However, an adequate receptor responsiveness is necessary to allow intracellular signalling and metabolic activity. We tested the ability of three-dimensionally arranged human hepatocytes to respond to the growth factors hepatocyte growth factor (HGF) or epidermal growth factor (EGF). Isolated adult human hepatocytes were cultivated within a three-dimensional collagen gel (sandwich) or on a two-dimensional collagen matrix. Cells were treated with HGF or EGF and expression and phosphorylative activity of HGF receptors (HGFr, c-met) or EGF receptors (EGFr) were measured by flow cytometry and Western blot. Increasing HGFr and EGFr levels were detected in hepatocytes growing two-dimensionally. However, both receptors were not activated in presence of growth factors. In contrast, when hepatocytes were plated within a three-dimensional matrix, HGFr and EGFr levels remained constantly low. However, both receptors became strongly phosphorylated by soluble HGF or EGF. We conclude that cultivation of human hepatocytes in a three-dimensionally arranged in vitro system allows the maintenance of specific functional activities. The necessity of cell dimensionality for HGFr and EGFr function should be considered when an adequate in vitro system has to be introduced for drug testing. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:527 / 532
页数:6
相关论文
共 21 条
[1]   Growth induction of hepatic stimulator substance in hepatocytes through its regulation on EGF receptors [J].
An, W ;
Liu, XJ ;
Lei, TG ;
Dai, J ;
Du, GG .
CELL RESEARCH, 1999, 9 (01) :37-49
[2]   Population expansion, clonal growth, and specific differentiation patterns in primary cultures of hepatocytes induced by HGF/SF, EGF and TGF alpha in a chemically defined (HGM) medium [J].
Block, GD ;
Locker, J ;
Bowen, WC ;
Petersen, BE ;
Katyal, S ;
Strom, SC ;
Riley, T ;
Howard, TA ;
Michalopoulos, GK .
JOURNAL OF CELL BIOLOGY, 1996, 132 (06) :1133-1149
[3]   Extracellular matrix and integrin signalling: the shape of things to come [J].
Boudreau, J ;
Jones, PL .
BIOCHEMICAL JOURNAL, 1999, 339 :481-488
[4]   An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons [J].
Brandon, EFA ;
Raap, CD ;
Meijerman, I ;
Beijnen, JH ;
Schellens, JHM .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 189 (03) :233-246
[5]   Effects of epidermal growth factor on CYP inducibility by xenobiotics, DNA replication, and caspase activations in collagen I gel sandwich cultures of rat hepatocytes [J].
De Smet, K ;
Loyer, P ;
Gilot, D ;
Vercruysse, A ;
Rogiers, V ;
Guguen-Guillouzo, C .
BIOCHEMICAL PHARMACOLOGY, 2001, 61 (10) :1293-1303
[6]   Induction of cytochrome P450 enzymes in cultured precision-cut human liver slices [J].
Edwards, RJ ;
Price, RJ ;
Watts, PS ;
Renwick, AB ;
Tredger, JM ;
Boobis, AR ;
Lake, BG .
DRUG METABOLISM AND DISPOSITION, 2003, 31 (03) :282-288
[7]   Mitogenic response to EGF of rat hepatocytes cultured on laminin-rich gels (EHS) is blocked downstream of receptor tyrosine-phosphorylation [J].
Gardner, MJ ;
Fletcher, K ;
Pogson, CI ;
Strain, AJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 228 (02) :238-245
[8]   Stability of cytochrome P450 proteins in cultured precision-cut rat liver slices [J].
Hashemi, E ;
Till, C ;
Ioannides, C .
TOXICOLOGY, 2000, 149 (2-3) :51-61
[9]  
Ilic D, 1997, J CELL SCI, V110, P401
[10]   Regulation of CYP2B6 and CYP3A expression by hydroxymethylglutaryl coenzyme a inhibitors in primary cultured human hepatocytes [J].
Kocarek, TA ;
Dahn, MS ;
Cai, HB ;
Strom, SC ;
Mercer-Haines, NA .
DRUG METABOLISM AND DISPOSITION, 2002, 30 (12) :1400-1405