Frontiers in Immunology (May 2017)

Impaired Autophagy and Defective T Cell Homeostasis in Mice with T Cell-Specific Deletion of Receptor for Activated C Kinase 1

  • Guihua Qiu,
  • Guihua Qiu,
  • Jian Liu,
  • Jian Liu,
  • Qianqian Cheng,
  • Qingyang Wang,
  • Zhaofei Jing,
  • Yujun Pei,
  • Min Zhao,
  • Jing Wang,
  • Jessie Yanxiang Guo,
  • Jiyan Zhang,
  • Jiyan Zhang

DOI
https://doi.org/10.3389/fimmu.2017.00575
Journal volume & issue
Vol. 8

Abstract

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Autophagy plays a central role in maintaining T cell homeostasis. Our previous study has shown that hepatocyte-specific deficiency of receptor for activated C kinase 1 (RACK1) leads to lipid accumulation in the liver, accompanied by impaired autophagy, but its in vivo role in T cells remains unclear. Here, we report that mice with T cell-specific deletion of RACK1 exhibit normal intrathymic development of conventional T cells and regulatory T (Treg) cells but reduced numbers of peripheral CD4+ and CD8+ T cells. Such defects are cell intrinsic with impaired mitochondrial clearance, increased sensitivity to cell death, and decreased proliferation that could be explained by impaired autophagy. Furthermore, RACK1 is essential for invariant natural T cell development. In vivo, T cell-specific loss of RACK1 dampens concanavalin A-induced acute liver injury. Our data suggest that RACK1 is a key regulator of T cell homeostasis.

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