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.

Alkaline Phosphatase-Positive Immortal Mouse Embryo Fibroblasts Are Cells in a Transitional Reprogramming State Induced to Face Environmental Stresses

M Evangelista
Primo
Methodology
;
M El Baroudi
Data Curation
;
M Rizzo
Methodology
;
L Poliseno;M Pellegrini
Membro del Collaboration Group
;
G Rainaldi
Ultimo
Conceptualization
2015

Abstract

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.
2015
Istituto di Fisiologia Clinica - IFC
Istituto di informatica e telematica - IIT
Inglese
7
1
33
41
9
https://journals.sagepub.com/doi/full/10.4137/GEG.S27696?rfr_dat=cr_pub++0pubmed&url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org
Esperti anonimi
immortal mouse embryonic fibroblasts, alkaline phosphatases, sestrin 1, cell cycle
Internazionale
Elettronico
No
7
info:eu-repo/semantics/article
262
Evangelista, M; EL BAROUDI, Mariama; Rizzo, M; Tuccoli, A; Poliseno, L; Pellegrini, M; Rainaldi, G
01 Contributo su Rivista::01.01 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/340791
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