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Faculty are listed by Department within their Research Areas,
with descriptions of their active projects.


ANATOMY AND NEUROBIOLOGY

JULIE SANDELL
Associate Professor of Anatomy and Neurobiology;
PhD, Massachusetts Institute of Technology

My lab has two major areas of interest: 1) we are part of a group that is building a retinal prosthesis to treat retinal degeneration and 2) we are interested in discovering the biological basis for cognitive impairment during normal aging. For the first project, we use anatomical techniques to investigate the remodeling that occurs in the retina in retinitis pigmentosa. We also study retinas from animals that have retinal degeneration as a result of a mutation, or as a result of a photoreceptor toxin. For the second project, we study the changes in neurons and neuroglial cells in the brain in monkeys as they age, and try to correlate the structural changes with the monkey's cognitive performance, which is determined in another laboratory. We are particularly interested in teasing apart the changes that are related to age alone from those that are related to cognitive status. Ultimately we would like to know what allows some individuals to age "successfully," while others are severely impaired. I also have long standing interests in visual system plasticity, and the role of GABA in neuronal development.

For more information regarding Julie Sandell's research and publications, please click on the following link:
http://www.bu.edu/dbin/anatneuro/our_people/faculty/sandell.php

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DEPARTMENT OF BIOLOGY

PAUL B. COOK
Assistant Professor of Biology; PhD, University of California, Berkeley

Processing of visual signals by the vertebrate retina involves interactions between excitatory and inhibitory neurons, the strength of which varies according to several parameters including the spatial properties of the cells and the temporal characteristics of their signals. In addition many of these interactions are modulated during changes in adaptational state such as the change in gap junction coupling between horizontal cells, or the responsiveness of retinal neurons to the excitatory neurotransmitter, glutamate.

In order to understand these interactions my laboratory employs several techniques including whole cell patch-clamp from retinal neurons in the flat mount/isolated retina and in the retinal slice preparations. Synaptic inputs can be elicited with stimuli such as patterned and random light stimuli, focal electrical stimulation of the retinal circuitry, and focal application of analogues, agonists and antagonists.

Computational models of neural function will complement the physiological studies. Particularly significant questions include the effects of anatomical constraints of the cells comprising specialized retinal circuits, effects of electrical coupling between neurons, the functional role of pre- and postsynaptic inhibition on shaping the temporal and spatial responses of cells, and the effects of modulation of synaptic inputs on retinal processing.

For more information regarding Paul B. Cook's research and publications, please click on the following link:
http://www.bu.edu/biology/Faculty_Staff/cook.html

VINCENT E. DIONNE

Professor of Biology; PhD, University of Arizona

Chemosensory physiology: research on the cellular mechanisms underlying the detection and discrimination of odors by olfactory receptor neurons in vertebrates. Electrophysiological, anatomical, histochemical, and molecular biological techniques are used in the laboratory.

For more information regarding Vincent E. Dionne's research and publications, please click on the following link:
http://www.bu.edu/biology/Faculty_Staff/vdionne.html

WILLIAM D. ELDRED
Professor of Biology; Professor in the Molecular Biology,
Cell Biology and Biochemistry Program; Professor in the
Program in Neuroscience; Department of Cognitive and Neural Systems
Research Fellow; PhD, University of Colorado Health Sciences Center

We are doing multidisciplinary studies of the role of cGMP in synaptic mechanisms in retinal neurons. These studies employ immunocytochemistry, retrograde tracers, intracellular injections, pharmacology, electrophysiology, biochemistry and image analysis at the light and electron microscopic levels. Particular emphasis is placed on regional differences in the retina and the biochemical and pharmacological mechanisms for modulating cGMP in identified neurons.

For more information regarding William D. Eldred's research and publications, please click on the following link:
http://www.bu.edu/biology/Faculty_Staff/eldred.html

JEN-WEI LIN
Professor of Biology; PhD, SUNY—Buffalo

Cellular and molecular mechanisms of neurotransmitter secretion
Neurotransmitter secretion is a complicated process that involves ion channel gating and secretion steps. In addition, the mobilization and recycling of synaptic vesicles are needed to maintain the function of a synapse and to contribute to synaptic plasticity. Ultimately, an understanding of the secretory events means that one can establish a kinetic scheme for this multi-step process and identify molecules responsible for each step. Therefore, a combined electrophysiological and molecular approach is used in my laboratory to investigate these questions.

For more information regarding Jen-Wei Lin's research and publications, please click on the following link:
http://www.bu.edu/biology/Faculty_Staff/jenwelin.html

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PHARMACOLOGY

DAVID H. FARB
Professor and Chairman of Pharmacology; PhD, Brandeis University

Abnormal activation of amino acid receptors has been implicated in the etiology of psychiatric disorders such as anxiety, depression and schizophrenia as well as of seizure disorders. Ongoing studies in the Farb lab provide a strong foundation for constructing models of steroid hormone interactions with excitatory and inhibitory amino acid receptors in the brain and spinal cord. This knowledge may lead to new strategies for the treatment of psychiatric and cognitive disorders. Although there is widespread medical and nonmedical use (and abuse) of steroids, there is very little information concerning the long-term effects of steroid exposure on the central nervous system. Rational drug design in conjunction with structural computational chemistry will be used to understand ligand receptor and DNA transcription factor recognition.

Dr. Farb's lab studies focuses on the mechanism of action of neuromodulators and on the structure, function, and cellular dynamics of amino acid receptors in the brain and spinal cord. Amino acid receptor function can be controlled by direct modulation of receptor function on the time scale of milliseconds to seconds and by regulation of receptor expression by genomic mechanisms. The role of neuroactive steroids in the control of GABA, glycine, and glutamate (NMDA and non-NMDA) receptors is being investigated using a multidisciplinary approach that includes the techniques of molecular biology, patch-clamp neurophysiology, cell biology, and molecular neuroanatomy. We have isolated segments of DNA from the human genome that contain the genetic blueprint for the production of GABA receptors. By determining the sequences for the regions of the gene that control its expression, we hope to be able to identify receptor-specific transcription factors and to design new classes of therapeutic agents that may act by regulating the expression of neurotransmitter receptors in the brain.

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