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Hepatocyte growth inhibitory factor derived from HTLV-I(+) T cell lines: effect on the epidermal growth factor-dependent proliferation of rat hepatocytes.

Abstract
A human T cell leukemia virus-I infected T cell line, ATL-2, produces an interleukin-2 receptor inducing factor, adult T cell leukemia (ATL)-derived factor (ADF). In the conditioned medium (CM) of ATL-2, we found an inhibitory activity on the epidermal growth factor (EGF)-dependent proliferation of primary cultured rat hepatocytes, measured by cell number and [3H]thymidine incorporation. ATL-2 CM dose-dependently inhibited hepatocyte proliferation. This activity was fractionated by gel filtration at a molecular size of 15,000 to 40,000 and was tentatively called hepatocyte growth inhibitory factor (HGI). Further fractionation with the ion-exchange column indicated that HGI was separable from ADF. Nevertheless, there was a positive correlation between HGI and ADF production, because the HGI activity was also detected in the CM of another ADF producer cell line (HUT102), while no significant HGI activity was detected in the CM of low ADF producer cell lines, ED and MOLT4.
AuthorsT Inamoto, A Yamauchi, H Nakamura, Y Nakamura, M Kanai, M Maeda, Y Tagaya, J Yodoi, K Ozawa
JournalClinical immunology and immunopathology (Clin Immunol Immunopathol) Vol. 58 Issue 3 Pg. 366-76 (Mar 1991) ISSN: 0090-1229 [Print] United States
PMID1900462 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cytokines
  • Interleukin-1
  • Interleukin-2
  • Neoplasm Proteins
  • Transforming Growth Factor beta
  • adult T cell leukemia-derived factor
  • Epidermal Growth Factor
  • Interferon-gamma
Topics
  • Animals
  • Cell Division (drug effects)
  • Cells, Cultured
  • Chromatography, Gel
  • Chromatography, High Pressure Liquid
  • Cytokines
  • Dose-Response Relationship, Drug
  • Epidermal Growth Factor (physiology)
  • Human T-lymphotropic virus 1 (metabolism)
  • In Vitro Techniques
  • Interferon-gamma (pharmacology)
  • Interleukin-1 (pharmacology)
  • Interleukin-2 (pharmacology)
  • Liver (drug effects, physiology)
  • Male
  • Neoplasm Proteins (pharmacology)
  • Rats
  • Rats, Inbred Strains
  • T-Lymphocytes (metabolism, microbiology)
  • Transforming Growth Factor beta (pharmacology)

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