About this item:

242 Views | 382 Downloads

Author Notes:

For correspondence: hyewon.phee@northwestern.edu

Author contributions: HP, Conception and design, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article. BBA-Y, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article. OP, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article. KLO'H, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article.

SGF, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article. MM, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article.

DC, Acquisition of data, Analysis and interpretation of data, Drafting or revising the article. MR, Analysis and interpretation of data, Drafting or revising the article, Contributed unpublished essential data or reagents.

RK, Analysis and interpretation of data, Drafting or revising the article, Contributed unpublished essential data or reagents.

JC, Analysis and interpretation of data, Drafting or revising the article, Contributed unpublished essential data or reagents. AW, Conception and design, Analysis and interpretation of data, Drafting or revising the article.

The authors would like to thank the Phee and Weiss laboratories for discussions. All microscopy studies were performed at Northwestern University Cell Imaging Facility.

The authors declare that no competing interests exist.

Subjects:

Research Funding:

This work was supported grants from US National Institutes of Health 5K01AR059754 (HP) and R01 CA142928 (JC), as well as the Howard Hughes Medical Institute (AW).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Biology
  • Life Sciences & Biomedicine - Other Topics
  • T-CELL-RECEPTOR
  • NUCLEOTIDE EXCHANGE FACTOR
  • KRUPPEL-LIKE FACTOR-2
  • VAV-FAMILY PROTEINS
  • BETA-CHAIN GENES
  • NEGATIVE SELECTION
  • POSITIVE SELECTION
  • THYMIC EMIGRATION
  • F-ACTIN
  • LYMPHOCYTE DEVELOPMENT

Pak2 is required for actin cytoskeleton remodeling, TCR signaling, and normal thymocyte development and maturation

Show all authors Show less authors

Tools:

Journal Title:

eLife

Volume:

Volume 3, Number 3

Publisher:

, Pages e02270-e02270

Type of Work:

Article | Final Publisher PDF

Abstract:

The molecular mechanisms that govern thymocyte development and maturation are incompletely understood. The P21-activated kinase 2 (Pak2) is an effector for the Rho family GTPases Rac and Cdc42 that regulate actin cytoskeletal remodeling, but its role in the immune system remains poorly understood. In this study, we show that T-cell specific deletion of Pak2 gene in mice resulted in severe T cell lymphopenia accompanied by marked defects in development, maturation, and egress of thymocytes. Pak2 was required for pre-TCR β-selection and positive selection. Surprisingly, Pak2 deficiency in CD4 single positive thymocytes prevented functional maturation and reduced expression of S1P1 and KLF2. Mechanistically, Pak2 is required for actin cytoskeletal remodeling triggered by TCR. Failure to induce proper actin cytoskeletal remodeling impaired PLCγ1 and Erk1/2 signaling in the absence of Pak2, uncovering the critical function of Pak2 as an essential regulator that governs the actin cytoskeleton-dependent signaling to ensure normal thymocyte development and maturation.

Copyright information:

© Phee et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 3.0 Unported License (http://creativecommons.org/licenses/by/3.0/).

Creative Commons License

Export to EndNote