Dr. Itzhak Mano

I study neuronal communication that uses the key excitatory neurotransmitter Glutamate, and the process of neuronal cell death that happen when the brain is flooded with too much of it. Excessive glutamate signaling triggers the neurodegeneration seen in prevalent neurodegenerative conditions such as stroke (a condition where minority communities are at special risk) and diseases like ALS/Lau Gehrig’s disease. We understand very little about this form of neuronal cell death, and although stroke leaves a window of opportunity for intervention physicians have no effective therapies to treat it. Minority populations are especially at high risk, as African-Americans at 4 times more likely to suffer a stroke in middle age, and have an overall double the risk of death from stroke compared to Caucasians. I examine normal and pathological glutamatergic neurotransmission in the microscopic free-living nematode C. elegans, because of the strong genetic research tools available in this model system. The basic premise is that although we look very different from nematodes, we share a great similarity at the cellular and molecular levels. Therefore, if we understand basic processes of normal physiology and Glutamate-induced pathologies in nematodes, it might give us clues as to possible similar processes in people. Trained as a neuroscientist and experienced in molecular biology, electrophysiology and model-system genetics, I analyze structure-function relations in transport proteins to learn how excess Glutamate is removed from the nervous system. I use genetic tools to study what are the molecular steps that lead from Glutamate over-excitation to neurodegeneration, and I study the ability to interfere with evolutionary-conserved signaling pathways (such as cell stress or autophagy) to protect the nervous system from Glutamate-induced neurodegeneration.




Dr. Itzhak Mano
Department of Sophie Davis School of Biomedical Education, Room H-309
City College of New York
138th Street & Convent Avenue
New York, NY 10031
t. 212.650.7965
t. 212.650.5334(lab)
f. 212.650.8585
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