Our laboratory is interested in understanding the
molecular mechanisms that underlie neuronal plasticity. Plasticity
is the property of the nervous system that enables it to undergo long-lasting,
sometimes permanent adaptive responses to brief stimuli. The process
of plasticity is believed to be important for establishing precise
patterns of synaptic connections during early neuronal development
and for learning and memory in older animals. Disturbances in plasticity
and synaptic function could contribute significantly to memory disorders
characteristic of some neurodegenerative diseases such as Huntington
disease and Alzheimer disease.
We are focusing on two problems related to plasticity. Work from several
laboratories has suggested that brief stimuli lead to lasting adaptive
responses in part through changes in new gene expression. We aim to
elucidate the signal transduction pathways by which specific stimuli
such as the influx of extracellular calcium or neurotrophin application
regulates synaptic function through gene transcription. As we identify
pathway components, we manipulate their function within neurons to
better understand the role that these molecules play in plasticity.
In a complementary approach, we are studying how a mutation in a single
gene leads to memory disturbances and neurodegeneration in the neurological
disorder, Huntington's disease. We have developed a cellular model
of the disease that has allowed us to manipulate the mutant gene to
better understand the relationship between its structure and function.
We use multiple approaches to study mechanisms of neuronal plasticity
and neurodegeneration. Molecular biology and biochemistry techniques
are used to identify and manipulate molecules that are involved in
these processes and electrophysiology and imaging techniques to test
the effects of these manipulations and to understand the roles of
these molecules in synaptic structure and function. |
Finkbeiner S, Tavazoie SF, Maloratsky A, Jacobs
K, Harris KM, Greenberg ME. CREB: a major mediator of neuronal neurotrophin
responses. Neuron 1997; 19:1031-47.
Tao X, Finkbeiner S, Arnold D, Shaywitz A, Greenberg
ME. Ca2+-influx regulates BDNF transcription by a CREB family transcription
factor-dependent mechanism. Neuron 1998; 20:709-26.
Saudou F*, Finkbeiner S*, Devys D, Greenberg ME.
Huntingtin acts in the nucleus to induce apoptosis but death does
not correlate with the formation of intranuclear inclusions. Cell
1998; 95:55-66.
Finkbeiner S. CREB couples neurotrophin signals to survival messages.
Neuron 2000; 25:11–14.
Finkbeiner, S. New roles for introns: sites of combinatorial regulation
of Ca2+- and cAMP-dependent gene expression. Science (STKE) 2001;
94:1–4.
Humbert S., Bryson, EA, Cordelières FP, Connors NC, Datta
SR, Finkbeiner S, Greenberg ME, Saudou F. The IGF-1/Akt pathway
is neuroprotective in Huntington’s Disease and involves huntingtin
phosphorylation by Akt. Dev. Cell 2002; 3:1–20.
Bradley J, Finkbeiner S. An evaluation of specificity in activity-dependent
gene expression in neurons. Prog Neurobiol 2002; 67:469-477.
information last updated September 2005 |