Milestone in the Regeneration of Brain Cells
News Aug 21, 2007
The research group of Prof. Dr. Magdalena Gotz at the Institute of Stem Cell Research of the GSF – National Research Centre for Environment and Health, and the Ludwig Maximilians University, Munich, has achieved an additional step for the potential replacement of damaged brain cells after injury or disease: functional nerve cells can be generated from astroglia, a type of supportive cells in the brain by means of special regulator proteins.
The majority of cells in the human brain are not nerve cells but star-shaped glia cells, the so called “astroglia”. “Glia means “glue”, explains Gotz. “As befits their name, until now these cells have been regarded merely as a kind of “putty” keeping the nerve cells together.
A couple of years ago, the research group had been already able to prove that these glia cells function as stem cells during development. This means that they are able to differentiate into functional nerve cells. However, this ability gets lost in later phases of development, so that even after an injury to the adult brain glial cells are unable to generate any more nerve cells.
In order to be able to reverse this development, the team studied what molecular switches are essential for the creation of nerve cells from glial cells during development. These regulator proteins are introduced into glial cells from the postnatal brain, which indeed respond by switching on the expression of neuronal proteins.
In his current work, Dr. Benedikt Berninger, was now able to show that single regulator proteins are quite sufficient to generate new functional nerve cells from glia cells. The transition from glia-to-neuron could be followed live at a time-lapse microscope. It was shown that glia cells need some days for the reprogramming until they take the normal shape of a nerve cell.
“These new nerve cells then have also the typical electrical properties of normal nerve cells”, emphasises Berninger. “We could show this by means of electrical recordings”.
“Our results are very encouraging, because the generation of correctly functional nerve cells from postnatal glia cells is an important step on the way to be able to replace functional nerve cells also after injuries in the brain,” underlines Magdalena Gotz.
Restoring the ability to walk following spinal cord injury requires neurons in the brain to reestablish communication pathways with neurons in the spinal cord, Mature neurons, however, are unable to regenerate their axons to facilitate this process. New research in mice shows one potential route to overcome this limitation may be by targeting liver kinase B1 (LKB1) protein.
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