Literature DB >> 23736538

Activation of the amino acid response modulates lineage specification during differentiation of murine embryonic stem cells.

Jixiu Shan1, Takashi Hamazaki, Tiffany A Tang, Naohiro Terada, Michael S Kilberg.   

Abstract

In somatic cells, a collection of signaling pathways activated by amino acid limitation have been identified and referred to as the amino acid response (AAR). Despite the importance of possible detrimental effects of nutrient limitation during in vitro culture, the AAR has not been investigated in embryonic stem cells (ESC). AAR activation caused the expected increase in transcription factors that mediate specific AAR pathways, as well as the induction of asparagine synthetase, a terminal AAR target gene. Neither AAR activation nor stable knockdown of activating transcription factor (Atf) 4, a transcriptional mediator of the AAR, adversely affected ESC self-renewal or pluripotency. Low-level induction of the AAR over a 12-day period of embryoid body differentiation did alter lineage specification such that the primitive endodermal, visceral endodermal, and endodermal lineages were favored, whereas mesodermal and certain ectodermal lineages were suppressed. Knockdown of Atf4 further enhanced the AAR-induced increase in endodermal formation, suggesting that this phenomenon is mediated by an Atf4-independent mechanism. Collectively, the results indicate that, during differentiation of mouse embryoid bodies in culture, the availability of nutrients, such as amino acids, can influence the formation of specific cell lineages.

Entities:  

Keywords:  activating transcription factor 4; embryoid bodies; endoderm; intrauterine growth restriction; protein restriction

Mesh:

Substances:

Year:  2013        PMID: 23736538      PMCID: PMC4116408          DOI: 10.1152/ajpendo.00136.2013

Source DB:  PubMed          Journal:  Am J Physiol Endocrinol Metab        ISSN: 0193-1849            Impact factor:   4.310


  53 in total

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Review 4.  Surviving Stress: Modulation of ATF4-Mediated Stress Responses in Normal and Malignant Cells.

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