Differential effects of interferon-gamma and low molecular weight BCGF on growth of human B lymphocytes; interferon-gamma prolongs the increased c-MYC mRNA levels after activation

Scand J Immunol. 1991 Apr;33(4):365-73. doi: 10.1111/j.1365-3083.1991.tb01783.x.

Abstract

We have characterized the growth-stimulating effect of Interferon-gamma (IFN-gamma) on various parameters of B cell growth, and compared the effects with those of low molecular weight B cell growth factor (lmw BCGF). We have found that IFN-gamma did not affect early changes induced by anti-mu, like initial calcium-flux and rise in mRNA-and protein levels of the proto-oncogene c-myc measured at 3 h. On the other hand, IFN-gamma enhanced the effect of anti-mu on parameters measured later in the G1 phase of the cell cycle, such as expression of the transferrin receptor and general transcriptional activity, measured as an increase in 7-aminoactinomycin D binding. In particular, whereas the c-myc levels in anti-mu-treated cells peaked at 3 h and then gradually declined, IFN-gamma together with anti-mu maintained the c-myc levels at 24 h at approximately the same levels as seen at 3 h. Overall, lmw BCGF had a more potent effect on the parameters affected by IFN-gamma, correlating with stronger enhancement of DNA synthesis. However, in contrast to IFN-gamma lmw BCGF did not affect anti-mu-induced c-myc mRNA levels. Thus this study has revealed differences between two B cell growth factors in effects on B cell cycle parameters.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Anti-Idiotypic / pharmacology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / physiology*
  • Blotting, Western
  • Calcium / metabolism
  • Cell Cycle / drug effects
  • Cell Cycle / immunology
  • Cell Division / drug effects
  • Cells, Cultured
  • DNA Replication / drug effects
  • Dactinomycin / analogs & derivatives
  • Dactinomycin / metabolism
  • Dose-Response Relationship, Drug
  • Fluorescent Dyes / metabolism
  • Gene Expression Regulation
  • Humans
  • Immunoglobulin M
  • In Vitro Techniques
  • Interferon-gamma / pharmacology*
  • Interleukin-4 / pharmacology*
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc / biosynthesis
  • Proto-Oncogene Proteins c-myc / genetics*
  • RNA, Messenger / drug effects*
  • Receptors, Transferrin / biosynthesis

Substances

  • Antibodies, Anti-Idiotypic
  • Fluorescent Dyes
  • Immunoglobulin M
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Receptors, Transferrin
  • Dactinomycin
  • Interleukin-4
  • 7-aminoactinomycin D
  • Interferon-gamma
  • Calcium