[ADAR1 Knockout Inhibits Notch1-induced T-ALL in Mice]

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2016 Jun;24(3):643-8. doi: 10.7534/j.issn.1009-2137.2016.03.002.
[Article in Chinese]

Abstract

Objective: To investigate the effect of ADAR1 on the occurrence and development of mouse T cell acute lymphoblastic leukemia (T-ALL).

Methods: Lck-Cre; ADAR1lox/lox mice were generated through interbreeding. The lineage-cells of Lck-Cre; ADAR1lox/lox mice and the control were enriched respectively by the means of MACS, and the lin- cells were transfected with retrovirus carrying MSCV-ICN1-IRES-GFP fusion gene. Then the transfection efficiency was detected by the means of FACS, and the same number of GFP+ cells were transplanted into lethally irradiated recipient mice to observe the survival of mice in 2 recipient group after transplantation.

Results: T cell-specific knockout ADAR1 mice were generated, and Notch1-induced T-ALL mouse model was established successfully. The leukemia with T-ALL characteristics occured in the mice of control group, but did not in the ADAR1 kmockout mice after transplantation.

Conclusions: ADAR1 plays a key role in the incidence and development of Notch1-induced T-ALL.

MeSH terms

  • Adenosine Deaminase / genetics*
  • Animals
  • Disease Models, Animal
  • Mice
  • Mice, Knockout
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma / genetics*
  • Receptor, Notch1 / genetics*
  • T-Lymphocytes

Substances

  • Notch1 protein, mouse
  • Receptor, Notch1
  • ADAR1 protein, mouse
  • Adenosine Deaminase