Studies on hepatocyte apoptosis, proliferation and oncogene c-fos expression in carbon tetrachloride-induced cirrhotic rat liver

Chen Libo , Yang Zhen , Qiu Fazu

Current Medical Science ›› 1999, Vol. 19 ›› Issue (1) : 53 -55.

PDF
Current Medical Science ›› 1999, Vol. 19 ›› Issue (1) : 53 -55. DOI: 10.1007/BF02895597
Article

Studies on hepatocyte apoptosis, proliferation and oncogene c-fos expression in carbon tetrachloride-induced cirrhotic rat liver

Author information +
History +
PDF

Abstract

To investigate the significance of hepatocyte apoptosis, proliferation and oncogene c-fos expression in carbon tetrachloride (CCl4)-induced cirrhotic rat liver. Rat cirrhosis was induced by subcutaneous injection of 50% (v:v 1:1) CCl4. Hepatocyte apoptosis, proliferation and oncogene c-fos expression were examined with TUNEL, PCNA and c-fos immunohistochemical methods in control group and treatment group 72 h, 5, 7, 11 and 15 weeks after CCl4, induction. Hepatocyte apoptosis was rarely seen in control rat liver. The hepatoeyte apoptosis was obviously increased 72 h after treatment. Fifteen weeks after treatment, the apoptosis was still more obvious in treatment group than that in controls. PCNA was constantly expressed in CCl4 group, with highest level at middle phase. C-fos was positive 7 and 11 weeks after CCl4 treatment. The results suggest that: 1) apoptosis is involved in rat liver damage at the early phase in CCl4-induced injury, and the process can alleviate nodule reconstruction or eradicate potentially mutational hepatocytes at the later phase; 2) hepatocytes constantly proliferate in CCl4-induced rat liver cirrhosis, especially at the middle phase; 3) c-fos might modulate hepatocyte proliferation in CCl4-induced rat liver cirrhosis.

Keywords

liver cirrhosis / apoptosis / cell proliferation / TUNEL / oncogene

Cite this article

Download citation ▾
Chen Libo, Yang Zhen, Qiu Fazu. Studies on hepatocyte apoptosis, proliferation and oncogene c-fos expression in carbon tetrachloride-induced cirrhotic rat liver. Current Medical Science, 1999, 19(1): 53-55 DOI:10.1007/BF02895597

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

TusharP, GoresG J. Apotosis and hepatobiliary diseases. Hepatol, 1995, 21(6): 1725-1725

[2]

BenzC, AngermullerS, Kloters-PlachkyP, et al. . Effect of S-adenosylmethionine versus tauroursodeoxycholic acid on bile acid-induced apoptosis and cytolysis in rat hepatocytes. Eur J Clin Invest, 1998, 28(7): 577-577

[3]

1984, 1(4):145

[4]

LeistM, GantnerF, BohlingerI, et al. . The bcl-2 protooncogene and the gastrointestinal epithelial tumor progression model. Am J Pathol, 1995, 146(1): 1220-1220

[5]

DelhayeM, LouisH, DegraefC, et al. . Relationship between hepatocyte proliferation activity and liver functional reserve in human cirrhosis. Hepatol, 1996, 23(5): 1003-1003

[6]

NagyP, BisgaardH G, RuginE S, et al. . In vivo infusion of growth factors enhances the mitogenic response of the hepatic ductal cells after administration of 2-acetylaminofluorene. Hepatol, 1996, 23(1): 840-840

[7]

NagoshiS, YasudaH, SudaJ, et al. . Hepatocyte apoptosis and hepatic expression of transforming growth factor-beta 1 mRNA during involution of hyperplastic rat liver induced by hepatocyte growth factor. J Gastroenterol Hepatol, 1998, 13(8): 786-786

[8]

EwicoA O, FioremtinoM, PonzettoA, et al. . Liver hepatocyte growth factor does not always correlate with hepatocellular proliferation in human liver lesions: its specific receptor c-met does. Hepatol, 1996, 24(1): 60-60

[9]

OgasawaraJ, WatanabeoF R, AdachiM, et al. . Lethal effect of the antiFAS antibody in mice. Nature, 1993, 364: 806-806

[10]

CollotaF, PollentaruttiN, SironiM, et al. . Expression and involvement of c-fos and c-jun protooncogenes in programmed cell death induced by growth factors deprivation in lymphoid cell lines. J Biol Chem, 1992, 267: 18-278

[11]

FerrerI, SeguiJ, OliveM. Strong c-Jun immunoreactivity is associated with apoptotic cell death in human tumors of the central nervous system. Neurosci Lett, 1996, 16,214(1): 49-49

[12]

BruccoleriA, GallucciR, GermolecD R, et al. . Induction of early-immediate genes by tumor necrosis factor alpha contribute to liver repair following chemical-induced hepatotoxicity. Hepatology, 1997, 25(1): 133-133

AI Summary AI Mindmap
PDF

97

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/