Phospholipase Cγ1 is required for pre-TCR signal transduction and pre-T cell development

Eur J Immunol. 2017 Jan;47(1):74-83. doi: 10.1002/eji.201646522. Epub 2016 Nov 7.

Abstract

Pre-T cell receptor (TCR) signaling is required for pre-T cell survival, proliferation, and differentiation from the CD4 and CD8 double negative (DN) to the double positive (DP) stage. However, the pre-TCR signal transduction pathway is not fully understood and the signaling molecules involved have not been completely identified. Phospholipase Cγ (PLCγ) 1 is an important signaling molecule that generates two second messengers, diacylglycerol and inositol 1,4,5-trisphosphate, that are important to mediate PKC activation and intracellular Ca2+ flux in many signaling pathways. Previously, we have shown that PLCγ1 is important for TCR-mediated signaling, development and T-cell activation, but the role of PLCγ1 in pre-TCR signal transduction and pre-T cell development is not known. In this study, we demonstrated that PLCγ1 expression level in pre-T cells was comparable to that in mature T cells. Deletion of PLCγ1 prior to the pre-TCR signaling stage partially blocked the DN3 to DN4 transition and reduced thymic cellularity. We also demonstrated that deletion of PLCγ1 impaired pre-T cell proliferation without affecting cell survival. Further study showed that deficiency of PLCγ1 impaired pre-TCR mediated Ca2+ flux and Erk activation. Thus our studies demonstrate that PLCγ1 is important for pre-TCR mediated signal transduction and pre-T cell development.

Keywords: Phospholipase Cγ1; Pre-T cell; Pre-TCR; Signal transduction; T-cell development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biomarkers
  • Calcium / metabolism
  • Cell Differentiation* / genetics
  • Cell Differentiation* / immunology
  • Cell Proliferation
  • Cell Survival / genetics
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Gene Expression
  • Genotype
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • Mice
  • Mice, Transgenic
  • Phospholipase C gamma / deficiency
  • Phospholipase C gamma / genetics
  • Phospholipase C gamma / metabolism*
  • Phosphorylation
  • Precursor Cells, T-Lymphoid / cytology*
  • Precursor Cells, T-Lymphoid / immunology
  • Precursor Cells, T-Lymphoid / metabolism*
  • Receptors, Antigen, T-Cell / genetics
  • Receptors, Antigen, T-Cell / metabolism*
  • Receptors, Antigen, T-Cell, alpha-beta / genetics
  • Receptors, Antigen, T-Cell, alpha-beta / metabolism
  • Signal Transduction*
  • Thymocytes / cytology
  • Thymocytes / immunology
  • Thymocytes / metabolism

Substances

  • Biomarkers
  • Receptors, Antigen, T-Cell
  • Receptors, Antigen, T-Cell, alpha-beta
  • Extracellular Signal-Regulated MAP Kinases
  • Phospholipase C gamma
  • Calcium