4.7 Article

Functional Compensation Between Myc and PI3K Signaling Supports Self- Renewal of Embryonic Stem Cells

期刊

STEM CELLS
卷 33, 期 3, 页码 713-725

出版社

WILEY-BLACKWELL
DOI: 10.1002/stem.1893

关键词

Embryonic stem cells; Pluripotency; Myc; PI3K; MAPK

资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan
  2. Japan Society for the Promotion of Science (JSPS)
  3. Leona M. and Harry B. Helmsley Charitable Trust [2012-PG-MED002]
  4. G. Harold and Leila Y. Mathers Charitable Foundation
  5. Salk Institute Cancer Center Support Grant
  6. Grants-in-Aid for Scientific Research [25293082, 26670162, 25670147, 26112512] Funding Source: KAKEN

向作者/读者索取更多资源

c-Myc and phosphatidylinositol 3-OH kinase (PI3K) both participate in diverse cellular processes, including cell cycle control and tumorigenic transformation. They also contribute to preserving embryonic stem cell (ESC) characteristics. However, in spite of the vast knowledge, the molecular relationship between c-Myc and PI3K in ESCs is not known. Herein, we demonstrate that c-Myc and PI3K function cooperatively but independently to support ESC self-renewal when murine ESCs are cultured under conventional culture condition. Interestingly, culture of ESCs in 2i-condition including a GSK3b and MEK inhibitor renders both PI3K and Myc signaling dispensable for the maintenance of pluripotent properties. These results suggest that the requirement for an oncogenic proliferation-dependent mechanism sustained by Myc and PI3K is context dependent and that the 2i-condition liberates ESCs from the dependence of this mechanism.

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