ENHANCEMENT OF TRANSFORMING GROWTH-FACTOR-BETA-1 EXPRESSION IN THE RAT PANCREAS DURING REGENERATION FROM CERULEIN-INDUCED PANCREATITIS

被引:87
作者
GRESS, T
MULLERPILLASCH, F
ELSASSER, HP
BACHEM, M
FERRARA, C
WEIDENBACH, H
LERCH, MM
ADLER, G
机构
[1] UNIV MARBURG, DEPT CELL BIOL, D-35037 MARBURG, GERMANY
[2] UNIV MARBURG, DEPT CLIN CHEM, D-35043 MARBURG, GERMANY
关键词
CERULEIN; EXTRACELLULAR MATRIX; PANCREATITIS; REGENERATION; TGF-BETA-1;
D O I
10.1111/j.1365-2362.1994.tb01060.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Synthesis of extracellular matrix components is enhanced in the rat pancreas during regeneration from caerulein-induced pancreatitis. To study the involvement of transforming growth factor beta 1 (TGF beta 1), one of the most potent modulators of the extracellular matrix, in the process of pancreatic regeneration we examined the expression of this gene on the transcript and protein level. Pancreatic RNA was extracted from rats killed 0h, 12h, 24h, 2, 3 and 7 days after induction of caerulein pancreatitis. Transcript levels for TGF beta 1 were measured by slot-blot analysis and mRNA in situ hybridization. Total amount of TGF beta 1-protein was measured using a radioligand binding assay. TGF beta 1 protein was increased twofold after 24 h and 48 h and returned to control values 7 days after induction of pancreatitis, TGF beta 1-mRNA reached maximal values (3-fold over controls) after 2 days. The largest amount of TGF beta 1-mRNA was found in pancreatic acinar cells and in stromal cells. In summary, expression of TGF beta 1 in acinar and stromal cells of the rat pancreas is enhanced during regeneration from caerulein-induced pancreatitis, which may indicate an involvement of TGF beta 1 in the regulation of extracellular matrix regeneration in the rat pancreas after caerulein-induced pancreatitis.
引用
收藏
页码:679 / 685
页数:7
相关论文
共 43 条
[1]   RFLP FOR THE HUMAN TRANSFORMING GROWTH-FACTOR BETA-1 GENE (TGFB) ON CHROMOSOME-19 [J].
ARDINGER, HH ;
ARDINGER, RH ;
BELL, GI ;
MURRAY, JC .
NUCLEIC ACIDS RESEARCH, 1988, 16 (16) :8202-8202
[2]   EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES [J].
ASSOIAN, RK ;
FLEURDELYS, BE ;
STEVENSON, HC ;
MILLER, PJ ;
MADTES, DK ;
RAINES, EW ;
ROSS, R ;
SPORN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6020-6024
[3]   TYPE-BETA TRANSFORMING GROWTH-FACTOR IN HUMAN-PLATELETS - RELEASE DURING PLATELET DEGRANULATION AND ACTION ON VASCULAR SMOOTH-MUSCLE CELLS [J].
ASSOIAN, RK ;
SPORN, MB .
JOURNAL OF CELL BIOLOGY, 1986, 102 (04) :1217-1223
[4]   ACTIVATION OF RAT-LIVER PERISINUSOIDAL LIPOCYTES BY TRANSFORMING GROWTH-FACTORS DERIVED FROM MYOFIBROBLASTLIKE CELLS - A POTENTIAL MECHANISM OF SELF PERPETUATION IN LIVER FIBROGENESIS [J].
BACHEM, MG ;
MEYER, D ;
MELCHIOR, R ;
SELL, KM ;
GRESSNER, AM .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 89 (01) :19-27
[5]  
BOCKMAN DE, 1992, INT J PANCREATOL, V12, P11
[6]   TRANSFORMING GROWTH-FACTOR-BETA IN DISEASE - THE DARK SIDE OF TISSUE-REPAIR [J].
BORDER, WA ;
RUOSLAHTI, E .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (01) :1-7
[7]   SUPPRESSION OF EXPERIMENTAL GLOMERULONEPHRITIS BY ANTISERUM AGAINST TRANSFORMING GROWTH FACTOR-BETA-1 [J].
BORDER, WA ;
OKUDA, S ;
LANGUINO, LR ;
SPORN, MB ;
RUOSLAHTI, E .
NATURE, 1990, 346 (6282) :371-374
[8]   NATURAL INHIBITOR OF TRANSFORMING GROWTH-FACTOR-BETA PROTECTS AGAINST SCARRING IN EXPERIMENTAL KIDNEY-DISEASE [J].
BORDER, WA ;
NOBLE, NA ;
YAMAMOTO, T ;
HARPER, JR ;
YAMAGUCHI, Y ;
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1992, 360 (6402) :361-364
[9]   TRANSFORMING GROWTH FACTOR-BETA MESSENGER-RNA INCREASES DURING LIVER-REGENERATION - A POSSIBLE PARACRINE MECHANISM OF GROWTH-REGULATION [J].
BRAUN, L ;
MEAD, JE ;
PANZICA, M ;
MIKUMO, R ;
BELL, GI ;
FAUSTO, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (05) :1539-1543
[10]   TRANSFORMING GROWTH FACTOR-BETA-1 IS PRESENT AT SITES OF EXTRACELLULAR-MATRIX GENE-EXPRESSION IN HUMAN PULMONARY FIBROSIS [J].
BROEKELMANN, TJ ;
LIMPER, AH ;
COLBY, TV ;
MCDONALD, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6642-6646