Skip NavigationSkip to Content

Mechanisms of Cytokine Signal Transduction - Il-2, Il-4 and Prolactin As Hematopoietin Receptor Models

  1. Author:
    Kirken, R. A.
    Evans, G. A.
    Duhe, R. J.
    Dasilva, L.
    Malabarba, M. G.
    Erwin, R. A.
    Farrar, W. L.
    1. Year: 1998
  1. Journal: Veterinary Immunology and Immunopathology
    1. 63
    2. 1-2
    3. Pages: 27-36
  2. Type of Article: Article
  1. Abstract:

    Cytokines, hormones and hematopoietic growth factors transduce biological signals across the cell membrane via a highly conserved family of single membrane-spanning receptors. The intracellular signal transducing machinery responsible for mediating these responses has remained largely unknown. However, recent identification of a homologous class of tyrosine kinases, Janus Kinases (JAKs), and a related family of transcription factors, signal transducers and activators of transcription (STATs), has shed new light on the molecular mechanisms responsible for mediating hematopoietin signaling and immune response. Current research efforts within the field of cytokine signaling have now shifted to understanding how these molecules are activated by hematopoietic receptors, positively and negatively regulated by kinases and phosphatases, and how they impact on gene transcription to ultimately coordinate cell homeostasis, proliferation and differentiation. This article will review some of our results identifying the involvement of JAKs, STATs, and secondary effector molecules activated following engagement of hematopoietic receptors for IL-2, IL-4, and prolactin. Here, we provide evidence for the ingenious ability of cytokine receptors to selectively recruit and activate these proteins among a repertoire of possible alternative biochemical messengers as a means to affect unique and general cell responses. (C) 1998 Elsevier Science B.V. All rights reserved. [References: 27]

    See More

External Sources

  1. No sources found.

Library Notes

  1. No notes added.
NCI at Frederick

You are leaving a government website.

This external link provides additional information that is consistent with the intended purpose of this site. The government cannot attest to the accuracy of a non-federal site.

Linking to a non-federal site does not constitute an endorsement by this institution or any of its employees of the sponsors or the information and products presented on the site. You will be subject to the destination site's privacy policy when you follow the link.

ContinueCancel