EXPRESSION OF SPARC IN NORMAL AND FIBROTIC LIVERS

被引:31
作者
FRIZELL, E
LIU, SL
ABRAHAM, A
OZAKI, I
EGHBALI, M
SAGE, EH
ZERN, MA
机构
[1] THOMAS JEFFERSON UNIV,JEFFERSON MED COLL,DEPT MED,PHILADELPHIA,PA 19107
[2] ROGER WILLIAMS MED CTR,DEPT MED,PROVIDENCE,RI
[3] BROWN UNIV,PROVIDENCE,RI 02912
[4] YALE UNIV,SCH MED,DEPT ANESTHESIOL,NEW HAVEN,CT 06510
[5] UNIV WASHINGTON,DEPT BIOL STRUCT,SEATTLE,WA 98195
关键词
D O I
10.1002/hep.1840210335
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
SPARC (secreted protein, acidic and rich in cysteine)-also known as osteonectin, BM-40, and 43K glycoprotein-is secreted by endothelial cells and fibroblasts in response to culture shock. SPARC has been found in association with tissues undergoing cell. proliferation, migration, and extracellular matrix-remodeling. We demonstrate that normal livers from humans, rats, and mice express substantial levels of SPARC messenger RNA (mRNA). Moreover, when compared with control specimens, significantly increased levels of SPARC mRNA were found in fibrotic Livers from two animal models of liver disease: murine schistosomiasis and carbon tetrachloride-induced fibrosis in rats. Fibrotic human livers also had markedly increased levels of SPARC mRNA in comparison with normal livers. We also detected an increased-production of SPARC protein in the liver of animals treated with carbon tetrachloride. By immunocytochemical analysis, SPARC protein was apparent in freshly isolated Ito cells. Hybridization studies showed Ito cells to be the main source of SPARC mRNA. Extracts from a Kupffer-endothelial cell fraction exhibited traces of SPARC transcript, but expression of SPARC mRNA was absent in extracts from freshly isolated hepatocytes. These studies demonstrate the increased expression of SPARC-a protein that modulates cell shape and disrupts cell-matrix interactions-during the initial stages of hepatic fibrosis.
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页码:847 / 854
页数:8
相关论文
共 66 条
[41]   DEVELOPMENTAL AND TRANSFORMATION-SENSITIVE EXPRESSION OF THE SPARC GENE ON MOUSE CHROMOSOME-11 [J].
MASON, IJ ;
MURPHY, D ;
MUNKE, M ;
FRANCKE, U ;
ELLIOTT, RW ;
HOGAN, BLM .
EMBO JOURNAL, 1986, 5 (08) :1831-1837
[42]   FOCAL ADHESION INTEGRITY IS DOWN-REGULATED BY THE ALTERNATIVELY SPLICED DOMAIN OF HUMAN TENASCIN [J].
MURPHYULLRICH, JE ;
LIGHTNER, VA ;
AUKHIL, I ;
YAN, YZ ;
ERICKSON, HP ;
HOOK, M .
JOURNAL OF CELL BIOLOGY, 1991, 115 (04) :1127-1136
[43]   CELLULAR-DISTRIBUTION OF TRANSFORMING GROWTH FACTOR-BETA-1 AND PROCOLLAGEN TYPE-1, TYPE-III, TYPE-IV TRANSCRIPTS IN CARBON TETRACHLORIDE-INDUCED RAT-LIVER FIBROSIS [J].
NAKATSUKASA, H ;
NAGY, P ;
EVARTS, RP ;
HSIA, CC ;
MARSDEN, E ;
THORGEIRSSON, SS .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 85 (06) :1833-1843
[44]   DEVELOPMENTAL EXPRESSION OF 2AR (OSTEOPONTIN) AND SPARC (OSTEONECTIN) RNA AS REVEALED BY INSITU HYBRIDIZATION [J].
NOMURA, S ;
WILLS, AJ ;
EDWARDS, DR ;
HEATH, JK ;
HOGAN, BLM .
JOURNAL OF CELL BIOLOGY, 1988, 106 (02) :441-450
[45]  
OGAWA K, 1986, AM J PATHOL, V125, P611
[46]  
OTSUKA K, 1984, J BIOL CHEM, V259, P9805
[47]  
RAMADORI G, 1990, HEPATOLOGY, V12, P920
[48]  
ROJKIND M, 1979, GASTROENTEROLOGY, V76, P710
[49]  
SAGE EH, 1991, J BIOL CHEM, V266, P14831
[50]   ENDOTHELIAL-CELL INJURY INVITRO IS ASSOCIATED WITH INCREASED SECRETION OF AN MR 43,000 GLYCOPROTEIN LIGAND [J].
SAGE, H ;
TUPPER, J ;
BRAMSON, R .
JOURNAL OF CELLULAR PHYSIOLOGY, 1986, 127 (03) :373-387