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Orchestrating stem cell fate: Novel tools for regenerative medicine
- Source :
- World Journal of Stem Cells
- Publication Year :
- 2019
- Publisher :
- Baishideng Publishing Group Inc., 2019.
-
Abstract
- Mesenchymal stem cells are undifferentiated cells able to acquire different phenotypes under specific stimuli. In vitro manipulation of these cells is focused on understanding stem cell behavior, proliferation and pluripotency. Latest advances in the field of stem cells concern epigenetics and its role in maintaining self-renewal and differentiation capabilities. Chemical and physical stimuli can modulate cell commitment, acting on gene expression of Oct-4, Sox-2 and Nanog, the main stemness markers, and tissue-lineage specific genes. This activation or repression is related to the activity of chromatin-remodeling factors and epigenetic regulators, new targets of many cell therapies. The aim of this review is to afford a view of the current state of in vitro and in vivo stem cell applications, highlighting the strategies used to influence stem cell commitment for current and future cell therapies. Identifying the molecular mechanisms controlling stem cell fate could open up novel strategies for tissue repairing processes and other clinical applications.
- Subjects :
- 0301 basic medicine
Homeobox protein NANOG
In vitro differentiation
Histology
Cell
Review
Stem cells
Clinical practice
Biology
Regenerative medicine
03 medical and health sciences
0302 clinical medicine
Physical stimuli
Stem cell fate
Genetics
medicine
Epigenetics
Molecular Biology
Psychological repression
Genetics (clinical)
Mesenchymal stem cell
Epigenetic
Cell Biology
Phenotype
Cell biology
030104 developmental biology
medicine.anatomical_structure
030220 oncology & carcinogenesis
Self-renewal
Cell transplantation
Stem cell
Subjects
Details
- ISSN :
- 19480210
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- World Journal of Stem Cells
- Accession number :
- edsair.doi.dedup.....44b446cf0952c0edcb88c023ec18f848
- Full Text :
- https://doi.org/10.4252/wjsc.v11.i8.464