Alkaline Phosphatase-Positive Immortal Mouse Embryo Fibroblasts Are Cells in a Transitional Reprogramming State Induced to Face Environmental Stresses
Author(s) -
Monica Evangelista,
Mariama El Baroudi,
Milena Rizzo,
Andrea Tuccoli,
Laura Poliseno,
Marco Pellegrini,
Giuseppe Rainaldi
Publication year - 2015
Publication title -
genetics and epigenetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.38
H-Index - 10
ISSN - 1179-237X
DOI - 10.4137/geg.s27696
Subject(s) - reprogramming , downregulation and upregulation , gene silencing , microbiology and biotechnology , alkaline phosphatase , embryonic stem cell , phosphatase , phenotype , biology , embryo , chemistry , gene , enzyme , genetics , biochemistry , phosphorylation
In this study, we report that immortal mouse embryonic fibroblasts (I-MEFs) have a baseline level of cells positive for alkaline phosphatase (AP(+)) staining. Environmental stresses, including long-lasting growth in the absence of expansion and treatment with drugs, enhance the frequency of AP(+) I-MEFs. By adapting fast red AP staining to the sorting procedure, we separated AP(+) and AP(-) I-MEFs and demonstrated that the differentially expressed genes are consistent with a reprogrammed phenotype. In particular, we found that sestrin 1 is upregulated in AP(+) I-MEFs. We focused on this gene and demonstrated that increased sestrin 1 expression is accompanied by the growth of I-MEFs in the absence of expansion and occurs before the formation of AP(+) I-MEFs. Together with sestrin 1 upregulation, we found that AP(+) I-MEFs accumulated in the G1 phase of the cell cycle, suggesting that the two events are causally related. Accordingly, we found that silencing sestrin 1 expression reduced the frequency and G1 accumulation of AP(+) I-MEFs. Taken together, our data suggested that I-MEFs stressed by environmental changes acquire the AP(+) phenotype and achieve a quiescent state characterized by a new transcriptional network.
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