Polyamines Help Control Embryonic Stem Cell Differentiation


Scientists from the Institute of Medical Biology (IMB), which is a research institute under the Agency for Science, Technology and Research (A*STAR), have made an important discovery about the role of molecules called “polyamines” in embryonic stem cells.

Polyamines are organic molecules that have more than one “amino” group (-NH2). These compounds have several functions inside cells. Since polyamines are highly positively changed, they bind the DNA, which is highly negatively changed. By binding to DNA, they stabilize the structure of DNA and aid with processes that are important for the life of cells, such as DNA replication (see Alm K and Oredssib S. Cells and polyamines do it cyclically. Essays Biochem. 2009 Nov 4;46:63-76). Plants without particular polyamines are more susceptible to drought (Yamaguchi K, et al., A protective role for the polyamine spermine against drought stress in Arabidopsis. Biochem Biophys Res Commun. 2007 Jan 12;352(2):486-90). Polyamine synthesis is extremely heavily regulated, and inhibition of polyamine synthesis causes cell growth to stop or greatly decrease. Polyamines also regulate ion channels in neurons, which mean that they can affect learning and memory.

How do polyamines affect embryonic stem cells? Remember that embryonic stem cells can divide indefinitely and, under the proper culture conditions, can stay in an undifferentiated state. A*STAR scientists found that in mouse embryonic stem cells, an enzyme called Amd1 is essential for maintenance of undifferentiated state and self-renewal. Amd1 catalyzes a reaction that is essential for polyamine synthesis.

For the interested, polyamines are made in a multistep process that begins with a molecule called “ornithine.” Ornithine is made from the amino acid arginine or by related processes. The removal of a carbon dioxide group from ornithine produces putrescine and the enzyme that catalyzes this reaction is ornithine decarboxylase (ODC). Putrescine is used to make two other polyamines called spermine and spermidine. To make spermidine and spermidine, propylamine groups must be added, and these are added by a molecule called S-adenosylmethionine (SAM). SAM is used in cells to add single carbon atoms to molecules, but polyamine synthesis uses SAM in a very unusual manner. The enzyme SAM decarboxylase removes a carbon dioxide from SAM to make dc-SAM, which stands for decarboxylated SAM. Two different enzymes act sequentially to add propylamine groups to putrescine. The first enzyme, spermidine synthase, adds the first propylamine group to make a molecule called spermidine, and the second, spermine synthase, adds the second propylamine to make spermine. Amd1 encodes the enzyme SAM decarboxylase.

According to the researchers at A*STAR, without high levels of Amd1, mouse embryonic stem cells are unable to properly stay in the undifferentiated state and divide. In order to drive embryonic stem cells to differentiate into nerve cells, Amd1 activity must decrease.

This is the first time, polyamines have been linked to embryonic stem cells function. Polyamines have been known for some time to play central roles in cancer and cell growth and division. This novel discovery, links polyamine regulation to ESC biology when the research team conducted a genome-wide screen to look for genes that were differentially controlled during embryonic stem cell differentiation.

The Principle Investigator at IMB, Leah Vardy, who was also the managing author on this paper, said, “The polyamines that Amd1 regulate have the potential to regulate many different aspects of self-renewal and differentiation. The next step is to understand in more detail the molecular targets of these polyamines both in embryonic stem cells and cells differentiating to different cellular lineages. It is possible that manipulation of polyamine levels in embryonic stem cells through inhibitors or activators of the pathway could help direct the differentiation of embryonic stem cells to more clinically useful cell types.”

The Executive Director of IMB, Birgitte Lane, noted, “This is a fine piece of fundamental research that will have breakthrough consequences in many areas and can bring about far-reaching applications. Developing cellular therapies is just one long-term clinical benefit of understanding ESC biology, which can also help develop stem cell systems for disease modeling, developing new drugs as well as a tool for researchers to answer other biological questions.”

Published by

mburatov

Professor of Biochemistry at Spring Arbor University (SAU) in Spring Arbor, MI. Have been at SAU since 1999. Author of The Stem Cell Epistles. Before that I was a postdoctoral research fellow at the University of Pennsylvania in Philadelphia, PA (1997-1999), and Sussex University, Falmer, UK (1994-1997). I studied Cell and Developmental Biology at UC Irvine (PhD 1994), and Microbiology at UC Davis (MA 1986, BS 1984).

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