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Sugar for the brain: Mechanism to prevent programmed cell death of nerve cells deciphered

Date:
January 16, 2012
Source:
Charité - Universitätsmedizin Berlin
Summary:
Scientists have deciphered a mechanism to prevent programmed cell death of nerve cells.

Oxygen and glucose are the food of our brain. If they are absent, such as during a stroke, nerve cells die. An international research team at Charité -- Universitätsmedizin Berlin, Germany, and McMaster University, Canada, has discovered a novel mechanism to prevent this cell death. The results of the study have now been published in the journal Proceedings of the National Academy of Sciences of the USA.

Brief periods of oxygen deprivation can act like a training session for cells in the human body. As a result, they are better able to survive longer periods of oxygen deprivation -- they are "prepared," so to speak. In addition, it is known that oxygen deficiency also affects sugar metabolism. However, sugar metabolism and programmed death of a cell so far have been regarded as independent events.

A research team led by the two scientists Philipp Mergenthaler and Andreas Meisel, who work together at the NeuroCure Cluster of Excellence at the Charité, now explains the link between these two processes. The survival of the cell is regulated by a key enzyme of sugar metabolism, the so-called hexokinase II. This enzyme alters the sugar nutrient glucose in such a way that it can be processed by the cell. The researchers discovered that this enzyme is activated in the nerve cells of the brain after a lack of oxygen. This happens, for example in the case of a stroke, a circulatory disorder of the brain, resulting in insufficient oxygen and nutrient supplies in the brain. The enzyme then plays a protective role. "This self-protection of the nerve cell represents an important basis for further research, from which it may be possible to develop optimized stroke therapies," says Meisel.

However, the molecular mechanisms of the oxygen deficiency and altered cellular metabolism not only play a role for stroke, but are also very important for tumor development and the defense against infections by the immune system. Consequently, the enzyme is held responsible for alterations in sugar metabolism of malignant tumors. However, if there is glucose deficiency in the cell and normal oxygen supplies, it can also cause cell death. "Understanding the basic mechanism of how sugar metabolism regulates cell death might thus be used to protect against stroke, but could also be used to selectively cause cell death in malignant tumors," Mergenthaler explains. The mechanism how sugar metabolism regulates cell death thus fundamentally expands the basic medical knowledge of many diseases.


Story Source:

The above story is based on materials provided by Charité - Universitätsmedizin Berlin. Note: Materials may be edited for content and length.


Journal Reference:

  1. P. Mergenthaler, A. Kahl, A. Kamitz, V. van Laak, K. Stohlmann, S. Thomsen, H. Klawitter, I. Przesdzing, L. Neeb, D. Freyer, J. Priller, T. J. Collins, D. Megow, U. Dirnagl, D. W. Andrews, A. Meisel. Mitochondrial hexokinase II (HKII) and phosphoprotein enriched in astrocytes (PEA15) form a molecular switch governing cellular fate depending on the metabolic state. Proceedings of the National Academy of Sciences, 2012; DOI: 10.1073/pnas.1108225109

Cite This Page:

Charité - Universitätsmedizin Berlin. "Sugar for the brain: Mechanism to prevent programmed cell death of nerve cells deciphered." ScienceDaily. ScienceDaily, 16 January 2012. <www.sciencedaily.com/releases/2012/01/120116112606.htm>.
Charité - Universitätsmedizin Berlin. (2012, January 16). Sugar for the brain: Mechanism to prevent programmed cell death of nerve cells deciphered. ScienceDaily. Retrieved July 29, 2014 from www.sciencedaily.com/releases/2012/01/120116112606.htm
Charité - Universitätsmedizin Berlin. "Sugar for the brain: Mechanism to prevent programmed cell death of nerve cells deciphered." ScienceDaily. www.sciencedaily.com/releases/2012/01/120116112606.htm (accessed July 29, 2014).

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