THE GENE OF HEPATOCYTE GROWTH-FACTOR IS EXPRESSED IN FAT-STORING CELLS OF RAT-LIVER AND IS DOWN-REGULATED DURING CELL-GROWTH AND BY TRANSFORMING GROWTH-FACTOR-BETA

被引:111
作者
RAMADORI, G [1 ]
NEUBAUER, K [1 ]
ODENTHAL, M [1 ]
NAKAMURA, T [1 ]
KNITTEL, T [1 ]
SCHWOGLER, S [1 ]
ZUMBUSCHENFELDE, KHM [1 ]
机构
[1] KYUSHU UNIV,FAC SCI,DEPT BIOL,FUKUOKA 812,JAPAN
关键词
D O I
10.1016/0006-291X(92)90545-V
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hepatocyte growth factor (HGF) has been detected in non-parenchymal cells but not in hepatocytes. We performed Northern blot analysis of total RNA extracted from rat hepatocytes, Kupffer cells, endothelial cells and fat-storing (Ito-) cells. Total RNA was extracted from fat-storing cells at different times after isolation and from cells treated with different amounts of transforming growth factor β. The RNA was hybridized with HGF, fibronectin-, and α-actin-specific cDNA probes, consecutively. We found an abundant amount of HGF mRNA in freshly isolated fat-storing cells, but not in other liver cells. The amount of the HGF transcripts decreases significantly in FSC during the time of culture, while fibronectin gene expression increases and α-actin gene expression as well. TGF-β dramatically inhibits HGF gene expression, but causes an enhanced fibronectin mRNA level. Northern blot hybridisation of total RNA from CCl4-chronically damaged liver with HGF cDNA shows a significant increase of HGF mRNA during development of liver fibrosis. We suggest that in damaged liver either non-parenchymal cells, others than FSC, became able to express the HGF in vivo, or other mediators overcome the inhibitory effect of TGF-β. © 1992.
引用
收藏
页码:739 / 742
页数:4
相关论文
共 27 条
[1]   NORTHERN BLOT NORMALIZATION WITH A 28S RIBOSOMAL-RNA OLIGONUCLEOTIDE PROBE [J].
BARBU, V ;
DAUTRY, F .
NUCLEIC ACIDS RESEARCH, 1989, 17 (17) :7115-7115
[2]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[3]  
FRIEDMAN SL, 1991, HEPATOLOGY, V14, P133
[4]   HEPATOCYTE GROWTH-FACTOR HEPATOPOIETIN-A STIMULATES THE GROWTH OF RAT-KIDNEY PROXIMAL TUBULE EPITHELIAL-CELLS (RPTE), RAT NONPARENCHYMAL LIVER-CELLS, HUMAN-MELANOMA CELLS, MOUSE KERATINOCYTES AND STIMULATES ANCHORAGE-INDEPENDENT GROWTH OF SV40-TRANSFORMED RPTE [J].
KAN, M ;
ZHANG, GH ;
ZARNEGAR, R ;
MICHALOPOULOS, G ;
MYOKEN, Y ;
MCKEEHAN, WL ;
STEVENS, JL .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 174 (01) :331-337
[5]   MARKED INCREASE OF HGF MESSENGER-RNA IN NON-PARENCHYMAL LIVER-CELLS OF RATS TREATED WITH HEPATOTOXINS [J].
KINOSHITA, T ;
TASHIRO, K ;
NAKAMURA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (03) :1229-1234
[6]  
MICHALOPOULOS G, 1984, CANCER RES, V44, P4414
[7]   LIVER-REGENERATION - MOLECULAR MECHANISMS OF GROWTH-CONTROL [J].
MICHALOPOULOS, GK .
FASEB JOURNAL, 1990, 4 (02) :176-187
[8]   MOLECULAR-CLONING AND SEQUENCE-ANALYSIS OF CDNA FOR HUMAN HEPATOCYTE GROWTH-FACTOR [J].
MIYAZAWA, K ;
TSUBOUCHI, H ;
NAKA, D ;
TAKAHASHI, K ;
OKIGAKI, M ;
ARAKAKI, N ;
NAKAYAMA, H ;
HIRONO, S ;
SAKIYAMA, O ;
TAKAHASHI, K ;
GOHDA, E ;
DAIKUHARA, Y ;
KITAMURA, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 163 (02) :967-973
[9]   MOLECULAR-CLONING AND EXPRESSION OF HUMAN HEPATOCYTE GROWTH-FACTOR [J].
NAKAMURA, T ;
NISHIZAWA, T ;
HAGIYA, M ;
SEKI, T ;
SHIMONISHI, M ;
SUGIMURA, A ;
TASHIRO, K ;
SHIMIZU, S .
NATURE, 1989, 342 (6248) :440-443
[10]  
NAKAMURA T, 1991, Progress in Growth Factor Research, V3, P67, DOI 10.1016/0955-2235(91)90014-U