Coupling of early response gene expression to distinct regulatory pathways during alpha-interferon and phorbol ester-induced plasmacytoid differentiation of B chronic lymphocytic leukaemia cells

FEBS Lett. 1990 Jul 16;267(2):242-4. doi: 10.1016/0014-5793(90)80935-c.

Abstract

Phorbol esters (phorbol 12-myristate 13-acetate; PMA) and alpha-interferon (alpha-IFN) act through divergent signal transduction pathways to induce B chronic lymphocytic leukaemia cells (B-CLL) to undergo plasmacytoid differentiation in vitro. By using a panel of PMA-inducible early response gene probes we show that these two different effectors are coupled to second messenger pathways that do not converge on a common gene regulatory programme in differentiation of B-CLL cells. Moreover, using the calcium ionophore, A23187, four distinct regulatory classes of early response gene could be defined implying that multiple regulatory pathways may mediate the process of terminal differentiation in B lymphocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / drug effects*
  • Blotting, Northern
  • Calcimycin / pharmacology
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Gene Expression Regulation, Leukemic / drug effects*
  • Genes, Regulator / drug effects
  • Humans
  • Interferon Type I / pharmacology*
  • Leukemia, Lymphocytic, Chronic, B-Cell / genetics*
  • Leukemia, Lymphocytic, Chronic, B-Cell / metabolism
  • Phorbol Esters / pharmacology*
  • Plasma Cells / drug effects
  • RNA, Messenger / metabolism
  • Second Messenger Systems / drug effects
  • Signal Transduction / drug effects
  • Tumor Cells, Cultured / drug effects

Substances

  • Interferon Type I
  • Phorbol Esters
  • RNA, Messenger
  • Calcimycin