“Progress in exploring new avenues for brain repair: Astroglia reprogrammed to generate synapse-forming neurons”

ScienceDaily (May 18, 2010)— A research team led by Professor Magdalena Götz and Dr. Benedikt Berninger of Helmholtz Zentrum München and Ludwig-Maximilians-Universität (LMU) Munich, reports a major step forward in discovering a therapy for neurodegenerative diseases such as Alzheimer’s or stroke. The researchers were able to convert glial cells of the brain into two different functional classes of neurons.

The findings are being published in the online, open access journal PLoS Biology.

Neurons are the cells in the brain which transmit information, while the astroglia (star-shaped glial cells) serve as a supportive scaffold and are involved in metabolism. Moreover, astroglia are closely related to radial glial cells, which during embryonic forebrain development function as precursors for most neurons. In fact, some glial cells even in the adult brain retain the capability of producing neurons — however these are only found in specific regions.

It is still not known exactly what differentiates normal astroglia from radial glial cells with neurogenic potential. However, the researchers led by Magdalena Götz, director of the Institute of Stem Cell Research at Helmholtz Zentrum München and chair of Physiological Genomics at LMU, have already shown in previous studies that astroglia from the cerebral cortex of young mice, which are normally incapable of generating neurons, can be driven to convert into neurons by forced expression of special regulatory proteins.

In this study, Götz and her team showed how astroglia can be directly converted into the two main classes of cortical neurons. This was made possible by the selective virus- mediated expression of specific proteins — transcription factors — which regulate the transcription of DNA. While the transcription factor neurogenin-2 directs the generation of excitatory neurons, the same astroglial cells yield inhibitory neurons after transduction of the transcription factor Dlx2.

“In this study we have succeeded in reprogramming the newly created neurons to the extent that they can now develop functioning synapses. These release — depending on the transcription factor used — either excitatory or inhibitory neurotransmitter substances,” said Dr. Christophe Heinrich, first author of the study. This process could not only be observed in young astroglia, but even in astroglia in the adult brain following tissue injury-induced reactivation.

“Our findings nurture the hope that the barrier separating the astroglial and neuronal cells — closely related as they are — is not insurmountable,” Dr. Berninger emphasized. Due to these encouraging results, the researchers intend to pursue this avenue further to gain new neurons from the glial cells present in the brain, in order to find therapies for neurodegenerative diseases such as Alzheimer’s.

Story Source:

Adapted from materials provided by Public Library of Science, via EurekAlert!, a service of AAAS.

Journal Reference:

  1. Christophe Heinrich, Robert Blum, Sergio Gascón, Giacomo Masserdotti, Pratibha Tripathi, Rodrigo Sánchez, Steffen Tiedt, Timm Schroeder, Magdalena Götz, Benedikt Berninger. Directing Astroglia from the Cerebral Cortex into Subtype Specific Functional Neurons. PLoS Biology, 2010; 8 (5): e1000373 DOI: 10.1371/journal.pbio.1000373

Note: If no author is given, the source is cited instead.

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