Preferential increase of extracellular matrix expression relative to transforming growth factor β1 in the pancreas during the early stage of acute hemorrhagic pancreatitis in rats

Pancreas

Volumn 35, Issue 4, 2007, Pages

  Nakamura, Hayato ^a,b   Tashiro, Mitsuo ^a,b   Yamaguchi, Taizo ^a,b   Asaumi, Hiroshi ^a,b   Nomiyama, Yoko ^a,b   Watanabe, Shiro ^a,b   Nagashio, Yoshikuni ^a,b   Miyamoto, Tamao ^a,b   Otsuki, Makoto ^a,b  

^a UNIVERSITY OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH   (Japan)

^b UNIVERSITY OF OCCUPATIONAL AND ENVIRONMENTAL HEALTH   (Japan)

Author keywords

Acute pancreatitis; Extracellular matrix; TGF 1

Indexed keywords

MESSENGER RNA; TAUROCHOLIC ACID; TRANSFORMING GROWTH FACTOR BETA1;

ACUTE HEMORRHAGIC PANCREATITIS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL ACTIVATION; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; EXTRACELLULAR MATRIX; MALE; NONHUMAN; NORTHERN BLOTTING; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN SECRETION; RAT; WESTERN BLOTTING;

ACUTE DISEASE; ANIMALS; COLLAGEN TYPE I; COLLAGEN TYPE IV; DISEASE MODELS, ANIMAL; EXTRACELLULAR MATRIX PROTEINS; FIBRONECTINS; HEMORRHAGE; MALE; PANCREAS; PANCREATITIS; PROCOLLAGEN; RATS; RATS, WISTAR; RNA, MESSENGER; TAUROCHOLIC ACID; TIME FACTORS; TRANSFORMING GROWTH FACTOR BETA1; UP-REGULATION;

EID: 37349014036     PISSN: 08853177     EISSN: 15364828     Source Type: Journal    
DOI: 10.1097/mpa.0b013e318120020d     Document Type: Article

References (45)

1. Border WA, Noble NA. Transforming growth factor β in tissue fibrosis. N Engl J Med. 1994;331:1286-1292.
2. Sporn MB, Roberts AB. Transforming growth factor-β: recent progress and new challenges. J Cell Biol. 1992;119:1017-1021.
3. Gressner AM, Bachem MG. Molecular mechanisms of liver fibrogenesis-a homage to the role of activated fat-storing cells. Digestion. 1995;56:335-346.
4. Pinzani M, Gesualdo L, Sabbah GM, et al. Effects of platelet-derived growth factor and other polypeptide mitogens on DNA synthesis and growth of cultured rat liver fat-storing cells. J Clin Invest. 1989;84:1786-1793.
5. Gress TM, Müller-Pillasch F, Elsässer HP, et al. Enhancement of transforming growth factor β 1 expression in the rat pancreas during regeneration from caerulein-induced pancreatitis. Eur J Clin Invest. 1994;24:679-685.
6. Riesle E, Friess H, Zhao L, et al. Increased expression of transforming growth factor βs after acute oedematous pancreatitis in rats suggests a role in pancreatic repair. Gut. 1997;40:73-79.
7. Steer ML, Meldolesi J. Pathogenesis of acute pancreatitis. Annu Rev Med. 1988;39:95-105.
8. Corfield AP, Cooper MJ, Williamson RC. Acute pancreatitis: a lethal disease of increasing incidence. Gut. 1985;26:724-729.
9. Schoenberg MH, Birk D, Beger HG. Oxidative stress in acute and chronic pancreatitis. Am J Clin Nutr. 1995;62(suppl):1306S-1314S.
10. Aho HJ, Koskensalo SM, Nevalainen TJ. Experimental pancreatitis in the rat. Sodium taurocholate-induced acute haemorrhagic pancreatitis. Scand J Gastroenterol. 1980;15:411-416.
11. Aho HJ, Nevalainen TJ, Aho AJ. Experimental pancreatitis in the rat. Development of pancreatic necrosis, ischemia and edema after intraductal sodium taurocholate injection. Eur Surg Res. 1983;15:28-36.
12. Reinhold D, Bank U, Buhling F, et al. A detailed protocol for the measurement of TGF-β1 in human blood samples. J Immunol Methods. 1997;209:203-206.
13. Müller-Pillasch F, Gress TM, Yamaguchi H, et al. The influence of transforming growth factor β1 on the expression of genes coding for matrix metalloproteinases and tissue inhibitors of metalloproteinases during regeneration from cerulein-induced pancreatitis. Pancreas. 1997;15:168-175.
14. Dumont N, Arteaga CL. The tumor microenvironment: a potential arbitrator of the tumor suppressive and promoting actions of TGF β. Differentiation. 2002;70:574-582.
15. Annes JP, Munger JS, Rifkin DB. Making sense of latent TGF β activation. J Cell Sci. 2003;116:217-224.
16. Munger JS, Harpel JG, Gleizes PE, et al. Latent transforming growth factor-β: structural features and mechanisms of activation. Kidney Int. 1997;51:1376-1382.
17. Konturek PC, Dembinski A, Warzecha Z, et al. Comparison of epidermal growth factor and transforming growth factor-β1 expression in hormone-induced acute pancreatitis in rats. Digestion. 1998;59:110-119.
18. Friedman SL, Yamasaki G, Wong L. Modulation of transforming growth factor β receptors of rat lipocytes during the hepatic wound healing response. Enhanced binding and reduced gene expression accompany cellular activation in culture and in vivo. J Biol Chem. 1994;269:10551-10558.
19. Jones CL, Buch S, Post M, et al. Renal extracellular matrix accumulation in acute puromycin aminonucleoside nephrosis in rats. Am J Pathol. 1992;141:1381-1396.
20. Desmouliere A, Geinoz A, Gabbiani F, et al. Transforming growth factor-β 1 induces α-smooth muscle actin expression in granulation tissue myofibroblasts and in quiescent and growing cultured fibroblasts. J Cell Biol. 1993;122:103-111.
21. Kimura Y, Trimura T, Ueno T, et al. Transforming growth factor β 1, extracellular matrix, and inflammatory cells in wound repair using a closed duodenal loop pancreatitis model rat. Immunohistochemical study. Scand J Gastroenterol. 1995;30:707-714.
22. Sparmann G, Merkord J, Jaschke A, et al. Pancreatic fibrosis in experimental pancreatitis induced by dibutyltin dichloride. Gastroenterology. 1997;112:1664-1672.
23. Kihara Y, Tashiro M, Nakamura H, et al. Role of TGF-β1, extracellular matrix, and matrix metalloproteinase in the healing process of the pancreas after induction of acute necrotizing pancreatitis using arginine in rats. Pancreas. 2001;23:288-295.
24. Tashiro M, Nakamura H, Taguchi M, et al. Oleic acid-induced pancreatitis alters expression of transforming growth factor-β1 and extracellular matrix components in rats. Pancreas. 2003;26:197-204.
25. Sanvito F, Nichols A, Herrera PL, et al. TGF-β 1 overexpression in murine pancreas induces chronic pancreatitis and, together with TNF-α, triggers insulin-dependent diabetes. Biochem Biophys Res Commun. 1995;217:1279-1286.
26. Lee MS, Gu D, Feng L, et al. Accumulation of extracellular matrix and developmental dysregulation in the pancreas by transgenic production of transforming growth factor-β 1. Am J Pathol. 1995;147:42-52.
27. Van Laethem JL, Robberecht P, Resibois A, et al. Transforming growth factor β promotes development of fibrosis after repeated courses of acute pancreatitis in mice. Gastroenterology. 1996;110:576-582.
28. Menke A, Yamaguchi H, Gress TM, et al. Extracellular matrix is reduced by inhibition of transforming growth factor β1 in pancreatitis in the rat. Gastroenterology. 1997;113:295-303.
29. Yoo BM, Yeo M, Oh TY, et al. Amelioration of pancreatic fibrosis in mice with defective TGF-β signaling. Pancreas. 2005;30:e71-e79.
30. Nagashio Y, Ueno H, Imamura M, et al. Inhibition of transforming growth factor β decreases pancreatic fibrosis and protects the pancreas against chronic injury in mice. Lab Invest. 2004;84:1610-1618.
31. Miyazono K, Heldin CH. Role for carbohydrate structures in TGF-β 1 latency. Nature. 1989;338:158-160.
32. Schultz-Cherry S, Lawler J, Murphy-Ullrich JE. The type 1 repeats of thrombospondin 1 activate latent transforming growth factor-β. J Biol Chem. 1994;269:26783-26788.
33. Lyons RM, Gentry LE, Purchio AF, et al. Mechanism of activation of latent recombinant transforming growth factor β1 by plasmin. J Cell Biol. 1990;110:1361-1367.
34. Munger JS, Huang X, Kawakatsu H, et al. The integrin α v β 6 binds and activates latent TGF β 1: a mechanism for regulating pulmonary inflammation and fibrosis. Cell. 1999;96:319-328.
35. Wahl SM, Hunt DA, Wakefield LM, et al. Transforming growth factor type β induces monocyte chemotaxis and growth factor production. Proc Natl Acad Sci U S A. 1987;84:5788-5792.
36. Roberts AB, Sporn MB, Assoian RK, et al. Transforming growth factor β: rapid induction of fibrosis and angiogenesis in vivo and stimulation of collagen formation in vitro. Proc Natl Acad Sci U S A. 1986;83:4167-4171.
37. Ristow HJ. BSC-1 growth inhibitor/type b transforming growth factor is a strong inhibitor of thymocyte proliferation. Proc Natl Acad Sci U S A. 1986;83:5531-5533.
38. Tsunawaki S, Sporn M, Ding A, et al. Deactivation of macrophages by transforming growth factor-β. Nature. 1988;334:260-262.
39. Taguchi M, Yamaguchi T, Otsuki M. Induction of PDX-1-positive cells in the main duct during regeneration after acute necrotizing pancreatitis in rats. J Pathol. 2002;197:638-646.
40. Apte MV, Haber PS, Applegate TL, et al. Periacinar stellate shaped cells in rat pancreas: identification, isolation, and culture. Gut. 1998;43:128-133.
41. Bachem MG. Identification, culture, and characterization of pancreatic stellate cells in rats and humans. Gastroenterology. 1998;115:421-432.
42. Rockey DC. Characterization of endothelin receptors mediating rat hepatic stellate cell contraction. Biochem Biophys Res Commun. 1995;207:725-731.
43. Helczynski L, Klos J, Wozniewicz B. Observation of collagen fibers in mesangial cells. Acta Med Pol. 1979;20:23-24.
44. Apte MV, Haber PS, Applegate TL, et al. Pancreatic stellate cells are activated by proinflammatory cytokines: implications for pancreatic fibrogenesis. Gut. 1999;44:534-541.
45. Watanabe S, Nagashio Y, Asaumi H, et al. Pressure activates rat pancreatic stellate cells. Am J Physiol Gastrointest Liver Physiol. 2004;287:G1175-G1181.