Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2012 Jul;90(7):735-45.
doi: 10.1007/s00109-012-0913-0. Epub 2012 May 30.

Human induced pluripotent stem cells--from mechanisms to clinical applications

Affiliations
Review

Human induced pluripotent stem cells--from mechanisms to clinical applications

Katharina Drews et al. J Mol Med (Berl). 2012 Jul.

Abstract

Human pluripotent stem cells hold great promise for basic research and regenerative medicine due to their inherent property to propagate infinitely, while maintaining the potential to differentiate into any given cell type of the human body. Since the first derivation in 1998, pluripotent human embryonic stem cells (ESCs) have been studied intensively, and although these cells provoke ethical and immune rejection concerns, translation of human ESC research into the clinics has been initiated. The generation of embryonic stem cell-like human induced pluripotent stem cells (iPSCs) from somatic cells by virus-mediated overexpression of distinct sets of reprogramming factors (OCT4, SOX2, KLF4, and c-MYC, or OCT4, SOX2, NANOG, and LIN28) in 2007 has opened up further opportunities in the field. While circumventing the major disputes associated with human ESCs, iPSCs offer the same advantages and, in addition, new perspectives for personalized medicine. This review summarizes technical advances toward the generation of potentially clinically relevant human iPSCs. We also highlight key molecular events underlying the process of cellular reprogramming and discuss inherent features of iPSCs, including genome instability and epigenetic memory. Furthermore, we will give an overview of particular envisaged human iPSC applications and point out which improvements are yet to come and what has been achieved so far.

PubMed Disclaimer

References

    1. Regen Med. 2010 Sep;5(5):799-807 - PubMed
    1. Drug Metab Dispos. 2003 Aug;31(8):1035-42 - PubMed
    1. Cell Stem Cell. 2009 Jul 2;5(1):111-23 - PubMed
    1. Nature. 2009 Apr 9;458(7239):766-70 - PubMed
    1. Lancet. 2012 Feb 25;379(9817):713-20 - PubMed

Publication types

LinkOut - more resources