Your browser doesn't support javascript.
loading
Sirtuin 5 is Dispensable for CD8+ T Cell Effector and Memory Differentiation.
Duan, Qianqian; Ding, Jiying; Li, Fangfang; Liu, Xiaowei; Zhao, Yunan; Yu, Hongxiu; Liu, Yong; Zhang, Lianjun.
Afiliación
  • Duan Q; Institute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Ding J; Suzhou Institute of Systems Medicine, Suzhou, China.
  • Li F; Institute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Liu X; Suzhou Institute of Systems Medicine, Suzhou, China.
  • Zhao Y; School of Life Science and Technology, China Pharmaceutical University, Nanjing, China.
  • Yu H; Institute of Systems Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
  • Liu Y; Suzhou Institute of Systems Medicine, Suzhou, China.
  • Zhang L; Institute of Biomedical Electromagnetic Engineering, Shenyang University of Technology, Shenyang, China.
Front Cell Dev Biol ; 9: 761193, 2021.
Article en En | MEDLINE | ID: mdl-34966740
ABSTRACT
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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2021 Tipo del documento: Article País de afiliación: China