Mika Ono 858-784-2052 mikaono@scripps.edu

Newswise LA JOLLA, CA April 22, 2013 In a serendipitous discovery, scientists at The Scripps Research Institute (TSRI) have found a way to turn bone marrow stem cells directly into brain cells.

Current techniques for turning patients marrow cells into cells of some other desired type are relatively cumbersome, risky and effectively confined to the lab dish. The new finding points to the possibility of simpler and safer techniques. Cell therapies derived from patients own cells are widely expected to be useful in treating spinal cord injuries, strokes and other conditions throughout the body, with little or no risk of immune rejection.

These results highlight the potential of antibodies as versatile manipulators of cellular functions, said Richard A. Lerner, the Lita Annenberg Hazen Professor of Immunochemistry and institute professor in the Department of Cell and Molecular Biology at TSRI, and principal investigator for the new study. This is a far cry from the way antibodies used to be thought ofas molecules that were selected simply for binding and not function.

The researchers discovered the method, reported in the online Early Edition of the Proceedings of the National Academy of Sciences the week of April 22, 2013, while looking for lab-grown antibodies that can activate a growth-stimulating receptor on marrow cells. One antibody turned out to activate the receptor in a way that induces marrow stem cellswhich normally develop into white blood cellsto become neural progenitor cells, a type of almost-mature brain cell.

Natures Toolkit

Natural antibodies are large, Y-shaped proteins produced by immune cells. Collectively, they are diverse enough to recognize about 100 billion distinct shapes on viruses, bacteria and other targets. Since the 1980s, molecular biologists have known how to produce antibodies in cell cultures in the laboratory. That has allowed them to start using this vast, target-gripping toolkit to make scientific probes, as well as diagnostics and therapies for cancer, arthritis, transplant rejection, viral infections and other diseases.

In the late 1980s, Lerner and his TSRI colleagues helped invent the first techniques for generating large libraries of distinct antibodies and swiftly determining which of these could bind to a desired target. The anti-inflammatory antibody Humira, now one of the worlds top-selling drugs, was discovered with the benefit of this technology.

Last year, in a study spearheaded by TSRI Research Associate Hongkai Zhang, Lerners laboratory devised a new antibody-discovery techniquein which antibodies are produced in mammalian cells along with receptors or other target molecules of interest. The technique enables researchers to determine rapidly not just which antibodies in a library bind to a given receptor, for example, but also which ones activate the receptor and thereby alter cell function.

Lab Dish in a Cell

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Antibody Transforms Stem Cells Directly into Brain Cells

Public release date: 21-Apr-2013 [ | E-mail | Share ]

Contact: Suzanne Price sprice@nutrition.org 617-954-3976 Federation of American Societies for Experimental Biology

Boston, MARudolf Jaenisch of the Whitehead Institute for Biomedical Research and Massachusetts Institute of Technology will speak at EB 2013 on the topic of stem cells, pluripotency and nuclear reprogramming. His work has led to major advances in our understanding of embryonic stem cells and "induced pluripotent stem" (IPS) cells, which appear identical to embryonic stem cells but can be created from adult cells without using an egg. Dr. Jaenisch will discuss the mechanism of in vitro reprogramming and the inefficiency of gene targeting on Sunday, April 21at 2:30 pm at the meeting of the American Association of Anatomists at Experimental Biology.

The stem cell field is no stranger to controversy and has become widely discussed for the cells' ability to generate any cell type. They offer a new way to study human development. "The greatest interest in using stem cells is for disease research," said Jaenisch. "In the late 1990s when Dolly was cloned, it was called therapeutic cloning. It is considered controversial for using human eggs and is technically difficult. With IPS cells, we now have a way to study the pathogenesis of disease in petri dishes, without human eggs."

According to Jaenisch, where Dolly was a theoretical solution, we now have new technology that makes it possible to move into application. IPS cells will allow scientists to study complex human diseases in Petri dishes, a step toward analyzing the conditions and developing therapies.

Another potential benefit from IPS cells is to use them for transplantation into a patient to cure disease possibly. "We can likely find a way to reduce the risk of organ/tissue rejection. We can also correct mutations in IPS cells," he added, which gives researchers one less complicating factor.

Jaenisch received his doctorate in medicine from the University of Munich in 1967. Before coming to Whitehead, he was head of the Department of Tumor Virology at the Heinrich Pette Institute at the University of Hamburg. He has coauthored more than 375 research papers and has received numerous prizes and recognitions, including an appointment to the National Academy of Sciences in 2003. He received the 2011 National Medal of Science.

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About Experimental Biology 2013

Experimental Biology's mission is to share the newest scientific concepts and research findings shaping future and current clinical advances and to give scientists and clinicians an unparalleled opportunity to hear from colleagues working on similar biomedical problems using different disciplines. With six sponsoring societies and another 20 U.S. and international guest societies, the annual meeting brings together scientists from throughout the United States and the world, representing dozens of scientific areas, from laboratory to translational to clinical research. The meeting also offers a wide spectrum of professional development sessions.

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Using induced pluripotent stem cells, scientists can better study human disease