Document Detail


Molecular basis of Mammalian embryonic stem cell pluripotency and self-renewal.
MedLine Citation:
PMID:  22649650     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
Mammalian embryonic stem cells (ESC) have a number of specific properties that make them a unique object of fundamental and applied studies. In culture, ESC can remain in an infinitely undifferentiated state and differentiate into descendants of all three germ layers - ectoderm, endoderm, and mesoderm - that is, they can potentially produce more than 200 cell types comprising the body of an adult mammal. These properties of ESC are refered to as self-renewal and pluripotency. In this review, the basic signal pathways implicated in the maintenance of ESC pluripotency are considered. The major genes comprising a subsystem of "internal regulators of pluripotency," their protein products and regulators, are characterized, and interaction with other factors is described as well. The role of epigenetic mechanisms and microRNAs in the system of ESC self-renewal and pluripotency, as well as the relationship between pluripotency and X-chromosome inactivation in female mammals, is discussed.
Authors:
S P Medvedev; A I Shevchenko; S M Zakian
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Acta naturae     Volume:  2     ISSN:  2075-8251     ISO Abbreviation:  Acta Naturae     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2012-05-31     Completed Date:  2012-08-23     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  101525823     Medline TA:  Acta Naturae     Country:  Russia (Federation)    
Other Details:
Languages:  eng     Pagination:  30-46     Citation Subset:  -    
Affiliation:
Institute of Cytology and Genetics, Siberian Branch, Russian Academy of Sciences.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Toll-Like Receptors (TLRs): The Role in Tumor Progression.
Next Document:  Protein engineering of penicillin acylase.