Skip to main content
Log in

Identification of expressed sequence tags of genes expressed highly in the activated hepatic stellate cell

  • Research Articles
  • Articles
  • Published:
Archives of Pharmacal Research Aims and scope Submit manuscript

Abstract

Expressed sequence tags (ESTs) were generated from two 3′-directed cDNA libraries constructed from quiescent and activated rat hepatic stellate cell (HSC) to analyze the expression profiles of active genes in both cells. From quiescent and activated HSC, 694 ESTs and 779 ESTs, respectively, were obtained after excluding those having shorter than 30 bp. Among ESTs obtained from quiescent and activated HSC, 68 and 73 kinds of ESTs (186 clones and 236 clones), respectively, appeared more than once, implying that their genes are expressed highly in each cell type. 52 among 73 ESTs appeared only in the activated HSC, 47 among 68 ESTs only in the normal HSC, and 21 in both cells. The genes of these 52 ESTs were assumed to be expressed more highly in the activated HSC. To confirm the high expression of genes of which the ESTs appeared more than twice in the activated HSC, northern hybridization was carried out with RNAs derived from rat normal and fibrotic liver using each of 18 EST DNAs as probe. 13 ESTs showed more intense bands with RNA isolated from the fibrotic liver than normal liver. From these results, we confirm the positive correlation between abundance of transcript in activated HSCs and the expression level in fibrotic liver. The expression profile of the transcripts serves as an important tool in understanding the biological properties of HSC.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bedossa, P., Ferlicot, S., Paradis, V., Dargere, D., Bonvoust, F., and Vidaud, M., Dystroglycan expression in hepatic stellate cells: role in liver fibrosis.Lab. Invest., 82, 1053–1061 (2002).

    PubMed  CAS  Google Scholar 

  • Benyon, R. C. and Arthur, M. J., Mechanisms of hepatic fibrosis.J. Pediatr. Gastroenterol. Nutr., 27, 75–85 (1998).

    Article  PubMed  CAS  Google Scholar 

  • Cassiman, D., Roskams, T., van Pelt, J., Libbrecht, L., Aertsen, P., Crabbe, T., Vankelecom, H., and Denef, C., Alpha B-crystallin expression in human and rat hepatic stellate cells.J. Hepatol., 35, 200–207 (2001).

    Article  PubMed  CAS  Google Scholar 

  • Eng, F. J. and Friedman, S. L., Fibrogenesis I. New insights into hepatic stellate cell activation: the simple becomes complex.Am. J. Physiol, Gastrointest. Liver Physiol., 279, G7-G11 (2000).

    CAS  Google Scholar 

  • El-Youssef, M., Mu, Y., Huang, L., Stellmach, V., and Crawford, S. E., Increased expression of transforming growth factor-betal and thrombospondin-1 in cogenital hepatic fibrosis: possible role of the hepatic stellate cell.J. Pediatr. Gastroenterol. Nutr., 28, 386–392 (1999).

    Article  PubMed  CAS  Google Scholar 

  • Friedman, S. L., Liver fibrogenesis and the role of hepatic stellate cells: new insights and prospects for therapy.J. Gastroenterol. Hepatol., 14, 618–633 (1999).

    Article  PubMed  Google Scholar 

  • Friedman, S. L., Molecular regulation of hepatic fibrosis, an integrated cellular response to tissue injury.J. Biol. Chem., 275, 2247–2250 (2000).

    Article  PubMed  CAS  Google Scholar 

  • Gressner, A. M., The cell biology of liver fibrogenesis - an imbalance of proliferation, growth arrest and apoptosis of myofibroblasts.Cell Tissue Res., 292, 447–452 (1998).

    Article  PubMed  CAS  Google Scholar 

  • Kawada, N., The hepatic perisinusoidal stellate cell.Histol. Histopathol., 12, 109–117 (1997).

    Google Scholar 

  • Lang, A., Schrum, L. W., Schoonhoven, R., Tuvia, S., Solis-Herruzo, J. A., Tsukamoto, H., Brenner, D. A., and Rippe, R. A., Expression of small heat shock protein alphaB-crystallin is induced after hepatic stellate cell activation.Am. J. Physiol. Gastrointest. Liver Physiol., 279, G1333-G1342 (2000).

    PubMed  CAS  Google Scholar 

  • Lee, S. H., Chae, K. S., Nan, J. X., and Sohn, D. H., The increment of purine specific sodium nucleotide cotransporter mRNA in experimental fibrotic liver induced by bile duct ligation and scission.Arch. Pharm. Res., 23, 613–619 (2000).

    PubMed  CAS  Google Scholar 

  • Lee, S. H., Seo, G. S., Park, P. H., Choi, J. Y., Park, Y. N., Kim, H. K., Chae, K. S., and Sohn, D. H., Increased expression ofO-acetyl disialoganglioside synthase during rat liver fbrogenesis relatesto stellate cell activation.BBRC, 303, 954–961 (2003).

    PubMed  CAS  Google Scholar 

  • Matsubara, K. and Okubo, K., cDNA analyses in the human genome project.Gene, 135, 265–274 (1993).

    Article  PubMed  CAS  Google Scholar 

  • Nakamura, H., Hirata, K., Yamashiro, K., Hiranuma, K., Shibata, K., Higashi, K., Morita, T., and Hirano, H., Increase of hepatic mRNAs of profiling, actin and extracellular matrix proteins after carbon tetrachloride treatment and partial hepatectomy in rats.BBRC, 198, 568–573 (1994).

    PubMed  CAS  Google Scholar 

  • Nan, J. X., Park, E. J., Lee, S. H., Park, P. H., Kim, J. Y., Ko, G., and Sohn, D. H., Antifibrotic effect of Stephania tetrandra on experimental liver fibrosis induced by bile duct ligation and scission in rats.Arch. Pharm. Res., 23, 501–506 (2000).

    Article  PubMed  CAS  Google Scholar 

  • Okubo, K., Hori, N., Matoba, R., Niiyama, T., Fukushima, K., Kojima, Y., and Matsubara, K., Large scale cDNA sequencing for analysis of quantitativeand qualitative aspects of gene expression.Nature Genet, 2, 173–179 (1992).

    Article  PubMed  CAS  Google Scholar 

  • Okubo, K., Utiyama, H., Hirano, T., Yoshii, J., and Matsubara, K., Expression profile of active genes in granulocytes.Blood, 92, 1432–1441 (1998).

    PubMed  Google Scholar 

  • Pinzani, M. and Gentilini, P., Biology of hepatic stellate cells and their possible relevance in the pathogenesis of portal hypertension in cirrhosis.Semin. Liver Dis., 19, 397–410 (1999).

    PubMed  CAS  Google Scholar 

  • Ratziu, V., Lalazar, A., Wong, L., Dang, Q., Collins, C., Shaulian, E., Jensen, S., and Friedman, S. L., Zf9, a kruppel-like transcription factor up-regulatedin vivo during early hepatic fibrosis.Proc. Natl. Acad. Sci. U.S.A., 95, 9500–9505 (1998).

    Article  PubMed  CAS  Google Scholar 

  • Ren, B., Zhu, H. Q., Luo, Z. F., Zhou, Q., Wang, Y., and Wang, Y. Z., Preliminary research on myosin light chain kinase in rabbit liver.World J. Gastroenterol., 7, 868–871 (2001).

    PubMed  CAS  Google Scholar 

  • Suzuki, E., Ota, T., Tsukuda, K., Okita, A., Matsuoka, K., Murakami, M., Doihara, H., and Schimizu, N., nm23-H1 reducesin vitro cell migration and the liver metastatic potential of colon cancer cells by regulating myosin light chain phosphorylation.Int. J. Cancer, 108, 207–211 (2004).

    Article  PubMed  CAS  Google Scholar 

  • Szebeni, A., Mehrotra, B., Baumann, A., Adam, S. A., Wingfield, P. T., and Olson, M. O., Nucleolar protein B23 stimulates nuclear import of the HIV-1 Rev protein and NLS-conjugated fnalbumin.Biochemistry, 36, 3941–3949 (1997).

    Article  PubMed  CAS  Google Scholar 

  • Velcuescu, V. E., Zhang, L., Vogelstein, B., and Kinzler, K. W., Serial analysis of gene expression.Science, 270, 484–487 (1995).

    Article  Google Scholar 

  • Virca, G. D., Northemann, W., Shiels, B. R., Widera, G., and Broome, S., Simplified northern blot hybridization using 5% sodium dodecyl sulfate.Bio.Techniques, 8, 370–371 (1990).

    CAS  Google Scholar 

  • Wang, D., Umekawa, H., and Olson, M. O., Expression and subcellular locations of two forms of nucleolar protein B23 in at tissues and cells.Cell Mol. Biol. Res., 39, 33–42 (1993).

    PubMed  CAS  Google Scholar 

  • Xu, R., Ho, Y. S., Ritchie, R. P., and Li, L., Human SM22 alpha 3AC encompasses regulatory sequences for expression in vascular and visceral smooth muscles at fetal and adult stages.Am. J. Physiol. Heart Circ. Physiol., 284, H1398–407 (2003).

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Dong Hwan Sohn.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lee, S.H., Chae, KS. & Sohn, D.H. Identification of expressed sequence tags of genes expressed highly in the activated hepatic stellate cell. Arch Pharm Res 27, 422–428 (2004). https://doi.org/10.1007/BF02980084

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF02980084

Key words

Navigation