4.7 Review

Functions of p53 in pluripotent stem cells

Journal

PROTEIN & CELL
Volume 11, Issue 1, Pages 71-78

Publisher

OXFORD UNIV PRESS
DOI: 10.1007/s13238-019-00665-x

Keywords

p53; embryonic stem cells; induced pluripotent stem cells; genetic stability; metabolism

Categories

Funding

  1. National Natural Science Foundation of China [815300045, 81871197, 81930084, 81430032, U1601222]
  2. National High Technology Research and Development Program (863 Program) [2015AA020310]
  3. Development and Reform Commission of Shenzhen Municipality [S2016004730009]
  4. Guangdong Innovative and Entrepreneurial Research Team Program [2016ZT06S638]
  5. Shenzhen Sanming Project of Medicine [SZSM201602102]

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Pluripotent stem cells (PSCs) are capable of unlimited self-renewal in culture and differentiation into all functional cell types in the body, and thus hold great promise for regenerative medicine. To achieve their clinical potential, it is critical for PSCs to maintain genomic stability during the extended proliferation. The critical tumor suppressor p53 is required to maintain genomic stability of mammalian cells. In response to DNA damage or oncogenic stress, p53 plays multiple roles in maintaining genomic stability of somatic cells by inducing cell cycle arrest, apoptosis, and senescence to prevent the passage of genetic mutations to the daughter cells. p53 is also required to maintain the genomic stability of PSCs. However, in response to the genotoxic stresses, a primary role of p53 in PSCs is to induce the differentiation of PSCs and inhibit pluripotency, providing mechanisms to maintain the genomic stability of the self-renewing PSCs. In addition, the roles of p53 in cellular metabolism might also contribute to genomic stability of PSCs by limiting oxidative stress. In summary, the elucidation of the roles of p53 in PSCs will be a prerequisite for developing safe PSC-based cell therapy.

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