Faculty & Research
- John Assad, Ph.D.
- Bruce P. Bean, Ph.D
- Richard T. Born, M.D.
- David Cardozo, Ph.D.
- David E. Clapham, M.D., Ph.D.
- Jonathan Cohen, Ph.D.
- David P. Corey, Ph.D.
- S. Robert Datta, M.D., Ph.D.
- Ruth Anne Eatock, Ph.D.
- Edwin J. Furshpan, Ph.D.
- Lisa V. Goodrich, Ph.D.
- Michael E. Greenberg, Ph.D.
- Chenghua Gu, D.V.M., Ph.D.
- Chris Harvey, Ph.D.
- David H. Hubel, M.D.
- Pascal S. Kaeser, M.D.
- Morris J. Karnovsky, M.B.B.CH., D.Sc.
- Joshua M. Kaplan, Ph.D
- Edward A. Kravitz, Ph.D.
- Margaret S. Livingstone, Ph.D.
- Qiufu Ma, Ph.D.
- Richard H. Masland, Ph.D.
- Joseph B. Martin, M.D., Ph.D.
- John H.R. Maunsell, Ph.D.
- David L. Paul, Ph.D.
- David D. Potter, Ph.D.
- Elio Raviola, M.D., Ph.D.
- Wade Regehr, Ph.D.
- R. Clay Reid, M.D., Ph.D.
- Bernardo Sabatini, M.D, Ph.D
- Thomas L. Schwarz, Ph.D.
- Rosalind Segal, M.D., Ph.D.
- Charles D. Stiles, Ph.D.
- Charles J. Weitz, M.D., Ph.D.
- Rachel I. Wilson , Ph.D.
- Clifford Woolf, M.D., Ph.D.
- Gary Yellen, Ph.D.
R. Clay Reid, M.D., Ph.D.
Professor of Neurobiology
Reid Lab Website: http://neuro.med.harvard.edu/site/reidweb/index.html
We study the general question of how visual information is transformed between the lateral geniculate nu-cleus of the thalamus (LGN) and layer 4 of the primary visual cortex. LGN cells receive visual input from one eye and are not sensitive to an object's orientation or direction of movement. Cortical cells often receive binocular inputs and are usually orientation and direction selective. We use a number of techniques to explore how these transformations come about.
In our electrophysiological studies, we record the activity of many individual neurons simultaneously in both thalamus and cortex. In the cat, we are studying the cortical mechanisms responsible for the selectivity for orientation and direction of motion in simple cells. In the macaque, we concentrate on the first stages of color processing in the cortex. We have found that the wiring of the direct inputs to cortex is extremely precise. Given the visual properties of any single layer 4 cortical neuron, virtually all of the thalamic neurons that would help it perform this function are directly connected to it. In order to study the facilitatory interactions between these multiple inputs to cortical neurons, we are currently using multielectrode arrays to record up to ten neurons in the thalamus along with several of their potential targets.
In related projects we are using optical imaging, a technique for mapping the function of neural populations in vivo. These studies produce maps of the visual cortex that show the clustering of neurons with different receptive field properties. Functional maps allow us to target specific types of neurons (such as color-selective cells in the macaque) for electrophysiological study.
Selected Publications:
Ohki, K, Chung, S, Ch'ng, YH, Kara, P, Reid, RC. (2005) Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex. Nature, In Press.
Kanold PO, Kara P, Reid RC, Shatz CJ (2003). Role of subplate neurons in functional maturation of visual cortical columns. Science 301: 521-525.
Kara P, Reid RC (2003) Efficacy of retinal spikes in driving cortical responses. J Neurosci. 23:8547-8557.
Reppas JB, Usrey WM and Reid RC (2002) Saccadic eye movements modulate visual responses in the lateral geniculate nucleus. Neuron, 35:961-974.
Alonso, JM, Usrey, WM and Reid, RC (2001) Rules of connectivity between geniculate cells and simple cells in cat primary visual cortex. J.
Neurosci. 21: 4002-4015.
Tavazoie ST and Reid RC (2000) Diverse receptive fields in the lateral geniculate nucleus during thalamocortical development. Nature Neurosci.
3:608-616.
Usrey WM, Reppas JB and Reid RC (1998) Paired-spike interactions and synaptic efficacy of retinal inputs to thalamus. Nature 395:384-387.
Reid RC and Alonso JM (1995) Specificity of monosynaptic connections from thalamus to visual cortex. Nature 378:281-284.