T helper differentiation proceeds through Stat1-dependent, Stat4-dependent and Stat4-independent phases

Curr Top Microbiol Immunol. 1999:238:13-26. doi: 10.1007/978-3-662-09709-0_2.

Abstract

Much of our focus in understanding Th1/Th2 development has been on the signals delivered by IL-12 and IL-4 as final determinants of terminal T cell differentiation. Because extinction of IL-12 signaling in early Th2 development could potentially be important in imprinting a more permanent Th2 phenotype on a population of T cells, we have also examined various parameters regulating the IL-12 signaling pathway. Whereas IL-4 appears to repress functional IL-12 signaling through inhibition of IL-12R beta 2 expression, IFN-gamma in the mouse, and IFN-alpha in the human appear to induce IL-12R beta 2 expression and promote IL-12 responsiveness. We propose that Th1 development can be considered in two stages, capacitance and development. Capacitance would simply involve expression of IL-12R beta 1 and beta 2 subunits, regulated by TCR, IL-4 and IFNs. The second stage, development, we propose is the true IL-12 induced developmental stage, involving expression of Stat4 inducible proteins. In the human, this may also occur via IFN-alpha, which is able to activate Stat4. It is perhaps possible that all of Stat4 actions on Th1 development may be exert directly by Stat4 at the IFN-gamma gene, however we suggest that, more likely, Stat4 may act to induce Th1 development through the induction of other non-cytokine genes, whose stable expression maintains the transcriptional state of a Th1 cell.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Animals
  • Antigens, Differentiation, T-Lymphocyte / physiology*
  • Cell Differentiation
  • DNA-Binding Proteins / physiology*
  • Humans
  • Immunologic Factors / metabolism
  • Interferon-alpha / physiology
  • Interferon-gamma / metabolism
  • Interleukin-12 / pharmacology
  • Interleukin-12 / physiology
  • Interleukin-4 / pharmacology
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred DBA
  • Mice, Transgenic
  • Phenotype
  • Receptors, Interleukin / antagonists & inhibitors
  • Receptors, Interleukin / metabolism
  • Receptors, Interleukin-12
  • STAT1 Transcription Factor
  • STAT4 Transcription Factor
  • Signal Transduction
  • T-Lymphocytes, Helper-Inducer / drug effects
  • T-Lymphocytes, Helper-Inducer / immunology*
  • Trans-Activators / physiology*

Substances

  • Antigens, Differentiation, T-Lymphocyte
  • DNA-Binding Proteins
  • Immunologic Factors
  • Interferon-alpha
  • Receptors, Interleukin
  • Receptors, Interleukin-12
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT4 Transcription Factor
  • STAT4 protein, human
  • Stat1 protein, mouse
  • Stat4 protein, mouse
  • Trans-Activators
  • Interleukin-12
  • Interleukin-4
  • Interferon-gamma