Abstract

The Tec family of tyrosine kinases transduces signals from antigen and other receptors in cells of the hematopoietic system. In particular, interleukin-2 inducible T cell kinase (Itk) plays an important role in modulating T cell development and activation. Itk is activated by receptors via a phosphatidylinositol 3-kinase-mediated pathway, which results in recruitment of Itk to the plasma membrane via its pleckstrin homology domain. We show here that membrane localization of Itk results in the formation of clusters of at least two molecules within 80 A of each other, which is dependent on the integrity of its pleckstrin homology domain. By contrast, the proline-rich region within the Tec homology domain, SH3 or SH2 domains, or kinase activity were not required for this event. More importantly, these clusters of Itk molecules form in distinct regions of the plasma membrane as only receptors that recruit phosphatidylinositol 3-kinase reside in the same membrane vicinity as the recruited Itk. Our results indicate that Itk forms dimers in the membrane and that receptors that recruit Itk do so to specific membrane regions.

Highlights

  • (Grants AI51626 and AI065566) and the American Heart Association (Grant 0330036N)

  • These kinases, including inducible T cell kinase (Itk), have a PH domain that allows them to be recruited to the plasma membrane by an activated PI3 kinase [1]

  • Membrane recruitment is a critical component of their activation, and Itk can be found at the plasma membrane of cells, other events are required for its full activity [17,18,19]

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Summary

Introduction

(Grants AI51626 and AI065566) and the American Heart Association (Grant 0330036N) We have examined these issues using a split YFP system [22] and find that Itk forms dimers or higher order clusters; it does so only at the plasma membrane and only in the vicinity of a receptor that can recruit PI3 kinase.

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