Cancers (Jul 2013)

Control of Oxidative Stress and Generation of Induced Pluripotent Stem Cell-like Cells by Jun Dimerization Protein 2

  • Naoto Yamaguchi,
  • Hiroyuki Miyoshi,
  • Hitomi Hasegawa,
  • Shigeo Saito,
  • Yukio Nakamura,
  • Chia-Chen Ku,
  • Shin-Wei Wang,
  • Ya-Han Yang,
  • Kenly Wuputra,
  • Yu-Mei Liao,
  • Cheng-Yi Lee,
  • Cheng-Lung Steve Lin,
  • Chee-Yin Chai,
  • Chun-Chieh Wu,
  • Li-Pin Kao,
  • Kung-Kai Kuo,
  • Ying-Chu Lin,
  • Deng-Chyang Wu,
  • Sophie Sheng-Wen Wang,
  • Shyh-Shin Chiou,
  • Chang-Sheng Lin,
  • Richard Eckner,
  • Kazunari K. Yokoyama

DOI
https://doi.org/10.3390/cancers5030959
Journal volume & issue
Vol. 5, no. 3
pp. 959 – 984

Abstract

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We report here that the Jun dimerization protein 2 (JDP2) plays a critical role as a cofactor for the transcription factors nuclear factor-erythroid 2-related factor 2 (Nrf2) and MafK in the regulation of the antioxidants and production of reactive oxygen species (ROS). JDP2 associates with Nrf2 and MafK (Nrf2-MafK) to increase the transcription of antioxidant response element-dependent genes. Oxidative-stress-inducing reagent led to an increase in the intracellular accumulation of ROS and cell proliferation in Jdp2 knock-out mouse embryonic fibroblasts. In Jdp2-Cre mice mated with reporter mice, the expression of JDP2 was restricted to granule cells in the brain cerebellum. The induced pluripotent stem cells (iPSC)-like cells were generated from DAOY medulloblastoma cell by introduction of JDP2, and the defined factor OCT4. iPSC-like cells expressed stem cell-like characteristics including alkaline phosphatase activity and some stem cell markers. However, such iPSC-like cells also proliferated rapidly, became neoplastic, and potentiated cell malignancy at a later stage in SCID mice. This study suggests that medulloblastoma cells can be reprogrammed successfully by JDP2 and OCT4 to become iPSC-like cells. These cells will be helpful for studying the generation of cancer stem cells and ROS homeostasis.

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