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Two Effective Routes for Removing Lineage Restriction Roadblocks: From Somatic Cells to Hepatocytes
- Source :
- International Journal of Molecular Sciences, International Journal of Molecular Sciences, Vol 16, Iss 9, Pp 20873-20895 (2015)
- Publication Year :
- 2015
- Publisher :
- MDPI, 2015.
-
Abstract
- The conversion of somatic cells to hepatocytes has fundamentally re-shaped traditional concepts regarding the limited resources for hepatocyte therapy. With the various induced pluripotent stem cell (iPSC) generation routes, most somatic cells can be effectively directed to functional stem cells, and this strategy will supply enough pluripotent material to generate promising functional hepatocytes. However, the major challenges and potential applications of reprogrammed hepatocytes remain under investigation. In this review, we provide a summary of two effective routes including direct reprogramming and indirect reprogramming from somatic cells to hepatocytes and the general potential applications of the resulting hepatocytes. Through these approaches, we are striving toward the goal of achieving a robust, mature source of clinically relevant lineages.
- Subjects :
- Lineage (genetic)
Somatic cell
induced pluripotent stem cells
Cell Culture Techniques
Cell- and Tissue-Based Therapy
Review
Biology
In Vitro Techniques
Catalysis
Inorganic Chemistry
lcsh:Chemistry
medicine
hepatocyte
Animals
Humans
Cell Lineage
Physical and Theoretical Chemistry
Precision Medicine
Induced pluripotent stem cell
Molecular Biology
lcsh:QH301-705.5
Spectroscopy
Genetics
Organic Chemistry
reprogramming
in vitro
General Medicine
differentiation
Cellular Reprogramming
Computer Science Applications
Cell biology
in vivo
medicine.anatomical_structure
lcsh:Biology (General)
lcsh:QD1-999
Cell culture
Hepatocyte
Cell Transdifferentiation
Hepatocytes
Stem cell
Reprogramming
Stem Cell Transplantation
Subjects
Details
- Language :
- English
- ISSN :
- 14220067
- Volume :
- 16
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- International Journal of Molecular Sciences
- Accession number :
- edsair.doi.dedup.....bfaef20050c6e02751de8e437dc45ad6