Adult Stem Cells Convert To Embryonic-like Stem Cells

Introduction

The simple recipe scientists earlier discovered for making adult stem cells behave like embryonic-like stem cells just got even simpler. A new report in the February 6th issue of the journal Cell, a Cell Press publication, shows for the first time that neural stem cells taken from adult mice can take on the characteristics of embryonic stem cells with the addition of a single transcription factor. Transcription factors are genes that control the activity of other genes.

Main Item

The simple recipe scientists earlier discovered for making adult stem cells behave like embryonic-like stem cells just got even simpler. A new report in the February 6th issue of the journal Cell, a Cell Press publication, shows for the first time that neural stem cells taken from adult mice can take on the characteristics of embryonic stem cells with the addition of a single transcription factor. Transcription factors are genes that control the activity of other genes.

The discovery follows a 2006 report also in the journal Cell that showed that the introduction of four ingredients could transform differentiated cells taken from adult mice into "induced pluripotent stem cells" (iPS) with the physical, growth, and genetic characteristics typical of embryonic stem cells. Pluripotent refers to the ability to differentiate into most other cell types. The same recipe was later shown to work with human skin cells as well.

Subsequent studies found that the four-ingredient recipe could in some cases be pared down to just two or three essential ingredients, said Hans Schaler of the Max Planck Institute for Molecular Biomedicine in Germany.

"Now we've come down to just one that is sufficient. In terms of the biology, it's really quite amazing."

The discovery sheds light on centuries-old questions about what distinguishes the embryonic stem cells that give rise to egg and sperm from other body cells, Schaler said. It might also have implications for the use of reprogrammed stem cells for replacing cells lost to disease or injury.

Other researchers led by Shinya Yamanaka showed that adult cells could be reprogrammed by adding four factors - specifically Oct4, Sox2, Klf4, and c-Myc. Recently, Schaler and his colleagues demonstrated that Oct4 and Klf4 are sufficient to induce pluripotency in neural stem cells.

By omitting Klf4 in the new study, they have now established that Oct4 is the "driving force" behind the conversion of the neural stem cells into iPS cells. The lone transcription factor is not only essential, but it is also sufficient to make neural stem cells pluripotent.

Those cells, which Schaler's team calls "1F iPS" can differentiate into all three germ layers. Those primary germ layers in embryos eventually give rise to all the body's tissues and organs. Not only can those cells efficiently differentiate into neural stem cells, heart muscle cells, and germ cells, they show, but they are also capable of forming tumors when injected under the skin of nude mice. Those tumors, or teratomas, contain tissue representing all three germ layers. When injected into mouse embryos, the 1F iPS cells also found their way into the animals' developing organs and were able to be transmitted through the germ line to the next generation, they report.

The results show that adult stem cells can be made pluripotent without c-Myc and Klf4, both of which are "bona fide" oncogenes that can help turn normal cells into cancer cells, Schaler said. Limiting the number of factors is also a bonus because it means fewer genes must be inserted into the genome, where they can potentially have detrimental effects.

"Strikingly, Oct4 alone is sufficient to induce pluripotency in neural stem cells, which demonstrates its crucial role in the process of reprogramming..." the researchers concluded. "Future studies will show whether other sources of neural stem or progenitor cell populations such as mouse or human bone marrow-derived mesenchymal stem cells or dental pulp can be reprogrammed to iPS cells and whether expression of Oct4 can be induced by non-retroviral means, a prerequisite for the generation of iPS cells of therapeutic value."

Researchers

The researchers included Jeong Beom Kim, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Vittorio Sebastiano, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Guangming Wu, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Marcos J. Arauzo-Bravo, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Philipp Sasse, University of Bonn, Bonn, Germany; Luca Gentile, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Kinarm Ko, Max Planck Institute for Molecular Biomedicine, Munster, Germany; David Ruau, RWTH Aachen University Medical School, Aachen, Germany; Mathias Ehrich, SEQUENOM Inc., San Diego, CA; Dirk van den Boom, SEQUENOM Inc., San Diego, CA; Johann Meyer, Hannover Medical School, Hannover, Germany; Karin Hubner, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Christof Bernemann, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Claudia Ortmeier, Max Planck Institute for Molecular Biomedicine, Munster, Germany; Martin Zenke, RWTH Aachen University Medical School, Aachen, Germany; Bernd K. Fleischmann, University of Bonn, Bonn, Germany; Holm Zaehres, Max Planck Institute for Molecular Biomedicine, Munster, Germany; and Hans R. Scholer, Max Planck Institute for Molecular Biomedicine, Munster, Germany.

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Attribution/Source(s): This peer reviewed publication was selected for publishing by the editors of Disabled World (DW) due to its relevance to the disability community. Originally authored by Cell Press and published on 2009/02/05, this content may have been edited for style, clarity, or brevity. For further details or clarifications, Cell Press can be contacted at cell.com NOTE: Disabled World does not provide any warranties or endorsements related to this article.