Frontiers in Cell and Developmental Biology (Dec 2021)

Sirtuin 5 is Dispensable for CD8+ T Cell Effector and Memory Differentiation

  • Qianqian Duan,
  • Qianqian Duan,
  • Jiying Ding,
  • Jiying Ding,
  • Jiying Ding,
  • Fangfang Li,
  • Fangfang Li,
  • Fangfang Li,
  • Xiaowei Liu,
  • Xiaowei Liu,
  • Yunan Zhao,
  • Hongxiu Yu,
  • Yong Liu,
  • Yong Liu,
  • Yong Liu,
  • Lianjun Zhang,
  • Lianjun Zhang,
  • Lianjun Zhang

DOI
https://doi.org/10.3389/fcell.2021.761193
Journal volume & issue
Vol. 9

Abstract

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CD8+ T cell effector and memory differentiation is tightly controlled at multiple levels including transcriptional, metabolic, and epigenetic regulation. Sirtuin 5 (SIRT5) is a protein deacetylase mainly located at mitochondria, but it remains unclear whether SIRT5 plays key roles in regulating CD8+ T cell effector or memory formation. Herein, with adoptive transfer of Sirt5+/+ or Sirt5−/− OT-1 cells and acute Listeria monocytogenes infection model, we demonstrate that SIRT5 deficiency does not affect CD8+ T cell effector function and that SIRT5 is not required for CD8+ T cell memory formation. Moreover, the recall response of SIRT5 deficient memory CD8+ T cells is comparable with Sirt5+/+ memory CD8+ T cells. Together, these observations suggest that SIRT5 is dispensable for the effector function and memory differentiation of CD8+ T cells.

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