Early alteration in TGF-β mRNA expression in irradiated rat liver

International Journal of Radiation Oncology Biology Physics

Volumn 46, Issue 3, 2000, Pages 639-643

  Seong, Jinsil ^a   Kim, Sung Hee ^a   Chung, Eun Ji ^a   Lee, Won Jae ^b   Suh, Chang Ok ^a  

^a Yonsei University College of Medicine   (South Korea)

^b Yonsei University College of Medicine   (South Korea)

Author keywords

Radiation induced hepatic fibrosis; TGF 1; TGF 3

Indexed keywords

MESSENGER RNA; TRANSFORMING GROWTH FACTOR BETA;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; DENSITOMETRY; GENE EXPRESSION; IMMUNOHISTOCHEMISTRY; LIVER FIBROSIS; MALE; NONHUMAN; PRIORITY JOURNAL; RADIATION INJURY; RAT; RNA ANALYSIS;

ANIMALS; BIOLOGICAL MARKERS; LIVER; LIVER CIRRHOSIS, EXPERIMENTAL; MALE; RADIATION DOSAGE; RADIATION INJURIES, EXPERIMENTAL; RADIOBIOLOGY; RATS; RATS, SPRAGUE-DAWLEY; RNA, MESSENGER; TIME FACTORS; TRANSFORMING GROWTH FACTOR BETA;

EID: 0343750667     PISSN: 03603016     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0360-3016(99)00401-0     Document Type: Article

References (27)

1. Ingold J.A., Reed G.B., Kaplan H.S., et al. Radiation hepatitis. Am J Roentgenol. 93:1965;200-208.
2. Lewin K., Millis R.R. Human radiation hepatitis A morphologic study with emphasis on the late changes . Arch Pathol. 96:1973;21-26.
3. Reed G.B., Cox A.J. The human liver after radiation injury A form of veno-occlusive disease . Am J Pathol. 48:1966;597-611.
4. Fajardo L.F., Colby T.V. Pathogenesis of veno-occlusive liver disease after radiation. Arch Pathol Lab Med. 104:1980;584-588.
5. Geraci J.P., Mariano M.S., Jackson K.L. Radiation hepatology of the rat Microvascular fibrosis and enhancement of liver dysfunction by diet and drugs . Radiat Res. 129:1992;322-332.
6. Withers H.R., Peters L.J., Kogelnik H.S. The pathobiology of late effects in irradiation. Meyn R.E., Withers H.R. Radiation biology in cancer research. 1980;439-448 Raven Press, New York.
7. Rubin P., Casarett G.W. Clinical radiation pathology. 1968;W.B. Saunders, Philadelphia.
8. Jaenke R.S., Robbins M.E., Bywaters T., et al. Capillary endothelium Target site of renal radiation injury . Lab Invest. 68:1993;396-405.
9. Schultheiss T.E., Stephens L.C. Permanent radiation myelopathy. Br J Radiol. 65:1992;737-753.
10. Rubin P., Finkelstein J., Shapiro D. Molecular biology mechanisms in the radiation induction of pulmonary injury syndromes Interrelationship between the alveolar macrophages and the septal fibroblast . Int J Radiat Oncol Biol Phys. 24:1992;93-101.
11. Finkelstein J.N., Johnston C.J., Baggs R., et al. Early alterations in extracellular matrix and transforming growth factor β gene expression in mouse lung indicative of late radiation fibrosis. Int J Radiat Oncol Biol Phys. 28:1994;621-631.
12. Rubin P., Johnston C.J., Williams J.P., et al. A perpetual cascade of cytokines postirradiation leads to pulmonary fibrosis. Int J Radiat Oncol Biol Phys. 33:1995;99-109.
13. Wang J., Robbins M.E.C. Radiation-induced alteration of rat mesangial cell transforming growth factor-β and expression of the genes associated with the extracellular matrix. Radiat Res. 146:1996;561-568.
14. Anscher M.S., Crocker J.R., Jirtle R.L. Transforming growth factor-beta 1 expression in irradiated liver. Radiat Res. 122:1990;77-85.
15. Geraci J.P., Mariano M.S. Radiation hepatology of the rat Parenchymal and nonparenchymal cell injury . Radiat Res. 136:1993;205-213.
16. Datta P.K., Moulder J.E., Fish B.L., et al. TGF-β1 production in radiation nephropathy Role of angiotensin II . Int J Radiat Biol. 75:1999;473-479.
17. Boumediene K., Vivien D., Macro M., et al. Modulation of rabbit articular chondrocyte (RAC) proliferation by TGF-β isoforms. Cell Prolif. 28:1995;221-234.
18. Huang J.X., Potts J.D., Vincent E.B., et al. Mechanisms of cell transformation in the embryonic heart. Ann NY Acad Sci. 752:1995;317-330.
19. Santana A., Saxena B., Noble N.A., et al. Increased expression of transforming growth factor β isoforms (β1, β2, β3) in bleomycin-induced pulmonary fibrosis. Am J Respir Cell Mol Biol. 13:1995;34-44.
20. Shah M., Foreman D.M., Ferguson M.W. Neutralisation of TGF-beta 1 and TGF-beta 2 or exogenous addition of TGF-beta 3 to cutaneous rat wounds reduces scarring. J Cell Sci. 108:1995;985-1002.
21. Murata H., Zhou L., Ochoa S., et al. TGF-β3 stimulates and regulates collagen synthesis through TGF-β1-dependent and independent mechanism. J Inves Dermatol. 108:1997;258-262.
22. Demirci G., Nashan B., Pichlmayr R. Fibrosis in chronic rejection of human liver allografts. Transplantation. 62:1996;1776-1783.
23. Bleser P.J., Niki T., Rogiers V., et al. Transforming growth factor-β gene expression in normal and fibrotic rat liver. J Hepatol. 26:1997;886-893.
24. Frank S., Madlener M., Werner S. Transforming growth factors β2, and β3 and their receptors are differentially regulated during normal and impaired wound healing. J Biol Chem. 271:1996;10188-10193.
25. Andres J.L., Stanley K., Cheifetz S., et al. Membrane-anchored and soluble forms of betaglucan, a polymorphic proteoglycan that binds transforming growth factor-beta. J Cell Biol. 109:1989;3137-3145.
26. Yamaguchi Y., Mann D.M., Ruoslahti E. Negative regulation of transforming growth factor beta by the proteoglycan decorin. Nature. 346:1990;281-284.
27. Gressner A.M., Bachem M.G. Molecular mechanisms of liver fibrogenesis A homage to the role of activated fat-storing cells . Digestion. 56:1995;335-346.