Regulation of asymmetric division and CD8+ T lymphocyte fate specification by protein kinase Cζ and protein kinase Cλ/ι

J Immunol. 2015 Mar 1;194(5):2249-59. doi: 10.4049/jimmunol.1401652. Epub 2015 Jan 23.

Abstract

During an immune response against a microbial pathogen, activated naive T lymphocytes give rise to effector cells that provide acute host defense and memory cells that provide long-lived immunity. It has been shown that T lymphocytes can undergo asymmetric division, enabling the daughter cells to inherit unequal amounts of fate-determining proteins and thereby acquire distinct fates from their inception. In this study, we show that the absence of the atypical protein kinase C (PKC) isoforms, PKCζ and PKCλ/ι, disrupts asymmetric CD8(+) T lymphocyte division. These alterations were associated with aberrant acquisition of a pre-effector transcriptional program, detected by single-cell gene expression analyses, in lymphocytes that had undergone their first division in vivo and enhanced differentiation toward effector fates at the expense of memory fates. Together, these results demonstrate a role for atypical PKC in regulating asymmetric division and the specification of divergent CD8(+) T lymphocyte fates early during an immune response.

Publication types

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

MeSH terms

  • Animals
  • CD8-Positive T-Lymphocytes / enzymology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / microbiology
  • CD8-Positive T-Lymphocytes / pathology
  • Cell Differentiation
  • Cell Division / immunology*
  • Dendritic Cells / immunology
  • Dendritic Cells / microbiology
  • Dendritic Cells / pathology
  • Gene Expression Regulation
  • Immunity, Innate*
  • Immunologic Memory
  • Isoenzymes / genetics
  • Isoenzymes / immunology*
  • Isoenzymes / metabolism
  • Listeria monocytogenes / immunology
  • Listeriosis / enzymology
  • Listeriosis / immunology*
  • Listeriosis / microbiology
  • Listeriosis / pathology
  • Mice
  • Mice, Knockout
  • Protein Kinase C / genetics
  • Protein Kinase C / immunology*
  • Protein Kinase C / metabolism
  • Signal Transduction
  • Single-Cell Analysis
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / microbiology
  • T-Lymphocyte Subsets / pathology

Substances

  • Isoenzymes
  • protein kinase C zeta
  • Protein Kinase C
  • protein kinase C lambda