During human fibrogenesis, myofibroblastlike cells proliferate and are the main source of fibrosis components. We have used cultured myofibroblastlike cells obtained by outgrowth from explants of human liver to study the expression of extracellular matrix (ECM) components and matrix-metalloproteinase-2 (MMP-2). These cells contained types I, III, IV, and V procollagen messenger RNAs (mRNAs). They also expressed mRNAs for laminin B1 chain and for cellular and plasma fibronectin. The corresponding proteins were detected by immuno-cytochemistry. MMP-2 expression was shown by Northern blot and gelatin zymography. Because transforming growth factor beta 1 (TGF beta 1) is considered an important mediator in liver fibrogenesis, we examined its effect on expression of ECM components by cultured human myofibroblastlike cells. TGF beta 1 increased collagen mRNAs steady-state levels and total collagen secretion in the culture medium. It also increased fibronectin mRNA levels but had no effect on laminin mRNA or (MMP-2 expression. In summary, cultured human myofibroblastlike cells express those ECM components that accumulate during hepatic fibrogenesis, indicating the usefulness of this model to study mechanisms of human liver fibrogenesis, In addition to the mitogenic effect of TGF beta 1 on human myofibroblastike cells, we now demonstrate its stimulation of ECM accumulation in these cells, thus emphasizing the central role of TGF beta 1 and myofibroblastlike cells in the pathophysiology of human hepatic fibrosis.
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
BALLARDINI, G
;
FALLANI, M
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
FALLANI, M
;
BIAGINI, G
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
BIAGINI, G
;
BIANCHI, FB
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
BIANCHI, FB
;
PISI, E
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
BALLARDINI, G
;
FALLANI, M
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
FALLANI, M
;
BIAGINI, G
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
BIAGINI, G
;
BIANCHI, FB
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UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY
BIANCHI, FB
;
PISI, E
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机构:
UNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALYUNIV BOLOGNA,POLICLIN S ORSOLA,IST CLIN MED 2,CATTEDRA SEMEIOT MED & ISTOL,V MASSARENTI 9,I-40138 BOLOGNA,ITALY