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

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...

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Detalles Bibliográficos
Autores principales: Chiou, Shyh-Shin, Wang, Sophie Sheng-Wen, Wu, Deng-Chyang, Lin, Ying-Chu, Kao, Li-Pin, Kuo, Kung-Kai, Wu, Chun-Chieh, Chai, Chee-Yin, Lin, Cheng-Lung Steve, Lee, Cheng-Yi, Liao, Yu-Mei, Wuputra, Kenly, Yang, Ya-Han, Wang, Shin-Wei, Ku, Chia-Chen, Nakamura, Yukio, Saito, Shigeo, Hasegawa, Hitomi, Yamaguchi, Naoto, Miyoshi, Hiroyuki, Lin, Chang-Sheng, Eckner, Richard, Yokoyama, Kazunari K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3795374/
https://www.ncbi.nlm.nih.gov/pubmed/24202329
http://dx.doi.org/10.3390/cancers5030959
Descripción
Sumario: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.