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Newswise Groups at the Weizmann Institute of Science and Cambridge University have jointly managed the feat of turning back the clock on human cells to create primordial germ cells the embryonic cells that give rise to sperm and ova in the lab. This is the first time that human cells have been programmed into this early developmental stage. The results of their study, which were published December 24 in Cell, could help provide answers as to the causes of fertility problems, yield insight into the earliest stages of embryonic development and potentially, in the future, enable the development of new kinds of reproductive technology.
Researchers have been attempting to create human primordial germ cells (PGCs) in the petri dish for years, says Dr. Jacob Hanna of the Weizmann Institutes Department of Molecular Genetics, who led the study together with research student Leehee Weinberger. PGCs arise within the early weeks of embryonic growth, as the embryonic stem cells in the fertilized egg begin to differentiate into the very basic cell types. Once these primordial cells become specified, they continue developing toward precursor sperm cells or ova pretty much on autopilot, says Dr. Hanna. The idea of creating these cells in the lab took off with the 2006 invention of induced pluripotent stem (iPS) cells adult cells that are reprogrammed to look and act like embryonic stem cells, which can then differentiate into any cell type. Thus several years ago, when researchers in Japan created mouse iPS cells and then got them to differentiate into PGCs, scientists immediately set about trying to replicate the achievement in human cells. But until now, none had been successful.
Previous research in Dr. Hannas lab pointed to new methods that could take human cells to the PGC state. That research had focused on the question of how human iPS cells and mouse embryonic cells differ: The mouse embryonic cells are easily kept in their stem cell state in the lab, while human iPS cells that have been reprogrammed a technique that involves the insertion of four genes have a strong drive to differentiate, and they often retain traces of priming. Dr. Hanna and his group then created a method for tuning down the genetic pathway for differentiation, thus creating a new type of iPS cell that they dubbed nave cells. These nave cells appeared to rejuvenate iPS cells one step further, closer to the original embryonic state from which they can truly differentiate into any cell type. Since these nave cells are more similar to their mouse counterparts, Dr. Hanna and his group thought they could be coaxed to differentiate into primordial germ cells.
Working with nave human embryonic stem and iPS cells, and applying the techniques that had been successful in the mouse cell experiments, the research team managed to produce cells that, in both cases, appeared to be identical to human PGCs. Together with the lab group of Prof. Azim Surani of Cambridge University, the scientists further tested and refined the method jointly in both labs. By adding a glowing red fluorescent marker to the genes for PGCs, they were able to gauge how many of the cells had been programmed. Their results showed that quite a high rate up to 40% had become PGCs; this quantity enables easy analysis.
Dr. Hanna points out that PGCs are only the first step in creating human sperm and ova. A number of hurdles remain before labs will be able to complete the chain of events that move an adult cell through the cycle of embryonic stem cell and around to sperm or ova. For one, at some point in the process, these cells must learn to perform the neat trick of dividing their DNA in half before they can become viable reproductive cells. Still, he is confident that those hurdles will one day be overcome, raising the possibility, for example, of enabling women who have undergone chemotherapy or premature menopause to conceive.
In the meantime, the study has already yielded some interesting results that may have significant implications for further research on PGCs and possibly other early embryonic cells. The team managed to trace part of the genetic chain of events that directs a stem cell to differentiate into a primordial germ cell, and they discovered a master gene, Sox17, that regulates the process in humans, but not in mice. Because this gene network is quite different from the one that had been identified in mice, the researchers suspect that more than a few surprises may await scientists who study the process in humans.
According to Dr. Hanna, Having the ability to create human PGCs in the petri dish will enable us to investigate the process of differentiation on the molecular level. For example, we found that only fresh nave cells can become PGCs; but after a week in conventional growth conditions they lose this capability once again. We want to know why this is. What is it about human stem cell states that makes them more or less competent? And what exactly drives the process of differentiation once a cell has been reprogrammed to its more nave state? It is the answers to these basic questions that will, ultimately, advance iPS cell technology to the point of medical use.
Dr. Jacob Hannas research is supported by Pascal and Ilana Mantoux, France/Israel; the New York Stem Cell Foundation; the Flight Attendant Medical Research Institute (FAMRI), the Israel Cancer Research Fund (ICRF); the Helen and Martin Kimmel Award for Innovative Investigation; the Benoziyo Endowment Fund for the Advancement of Science; the Leona M. and Harry B. Helmsley Charitable Trust; the Sir Charles Clore Research Prize; Erica A. Drake and Robert Drake; the Abisch Frenkel Foundation for the Promotion of Life Sciences; the European Research Council; the Israel Science Foundation, and the Fritz Thyssen Stiftung. Dr. Hanna is a New York Stem Cell Foundation-Robertson Investigator.
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