VVRC Website
About VVRC
People
News at VVRC
Vision Training
Vision Seminars
Research Services
Research Links



Anna Wang Roe's Website
Publications & Conferences
Laboratory Members
Web Links
Curriculum Vitae
Courses


Updated: Mon, Apr 16, 2012

“Interfacing mind and machine: Neuronal circuitry underlying visual and tactile perception”.

My lab studies the neuronal circuitry and functional organization underlying visual and tactile behavior in awake, behaving monkeys. To map these functions in the brain, we use an array of optical imaging, fMRI, electrophysiological, anatomical and optogenetics methods. Chronic implanted windows on the brain permit: 1) study of sensory and attentional processes and 2) methods to influence brain activity with electrical, laser, and optogenetic stimulation methods. This combined behavioral, functional, anatomical, and neuroengineering approach will lead to development of future mind-machine interfaces that modify and enhance function in normal and diseased states.

Anna Wang Roe
Office: 066 Wilson Hall
Phone: (615) 343-0901
E-mail: anna.roe@vanderbilt.edu

Feature Article: Identifying laminar cytoarchitecture via MR microscopy in awake monkeys

Brodmann divided the neocortex into 47 different cortical areas based on differences in laminar myeloarchitecture and cytoarchitecture. The ability to do so in vivo with anatomical magnetic resonance (MR) methods in awake subjects would be extremely advantageous. We used a combination of MR microscopy and new MR contrasts at 4.7 T with voxel size of 62.5 × 62.5 × 1000 μm3 to image visual cortex of awake Macaque monkeys. Both the phase and magnitude components of the T2*-weighted image were used to generate laminar profiles reflecting differential myelin and local cell density content across cortical depth. Based on this, we were able to infer the six layered laminar structure characteristic of V1,

including the stripe of Kaes-Bechterew (in layer II/III), the stripe of Gennari (in layer IV), the internal band of Baillarger (in layer V), as well as three sub-layers within layer IV (IVa, IVb, and IVc). Based on their laminar profiles, areas V1, V2, and V4 in awake macaques could also be distinguished. Following the tradition of Brodmann, MR-based cortical laminar visualization will make it possible to discriminate cortical regions in awake subjects based on differences in myeloarchitecture and cytoarchitecture. From

Chen G, Wang F, Gore, JC, Roe AW (2011) Identification of cortical lamination in awake  monkeys by high resolution magnetic resonance imaging. Neuroimage. 2011 Nov 3.


Feature Article: Motion maps in Macaque V2
In mammals, the perception of motion starts with direction-selective neurons in the visual cortex. Despite numerous studies in monkey V1 and V2 (primary and second visual cortex), there has been no evidence of direction maps in these areas. In the present study, we used optical imaging methods to study the organization of motion response in Macaque monkey V1 and V2. In contrast to the findings in other mammals (e.g. cats and ferrets), we found no direction maps in macaque V1. Robust direction maps, however, were found in V2 thick/pale stripes and avoided thin stripes. In many cases direction maps were located within thick stripes and exhibited pinwheel or linear organizations. The presence of motion maps in V2 points to a new found prominence of V2 in motion processing, either for contributing to motion perception in the dorsal pathway and/or for motion-cue dependent form perception in the ventral pathway.

Lu HD, Chen GC, Tanigawa H, Roe AW (2010) A motion direction map in Macaque V2, Neuron, 68(5):1002-1013.

Feature Article: Functional organization of V4

Visual area V4 in the macaque monkey contains a diverse complement of cells, including those with preference for color, orientation, disparity, as well as higher order feature preferences. However, unlike V1 and V2, it is unknown whether V4 is characterized by any distinct functional organizations. Here, using intrinsic signal optical imaging methods in awake, behaving monkeys, we demonstrate that functional organization for preferential response to color or luminance are largely separate from orientation selective regions. Color preference domains are characterized by the presence of hue maps. These results help resolve long-standing controversies regarding functional diversity and retinotopy within V4 and indicate the presence of spatially distinct distribution of featural representation in V4 in the ventral visual pathway.

Tanigawa H, Lu HD, Roe AW (2010) Functional organization for color and orientation in macaque V4. Nature Neurosci, 13(12):1542-8.

Feature Book: Imaging the Brain with Optical Methods

Imaging the Brain with Optical Methods presents the history of optical imaging and its use in the study of brain function, and the rapidly developing optical technologies and their applications that have recently developed. These include intrinsic signal optical imaging, near-infrared optical imaging, fast optical imaging based on scattered light, optical imaging with voltage sensitive dyes, and 2 photon imaging of hemodynamic signals.

Roe AW (2009) Imaging the Brain with Optical Methods (Roe AW, ed). Springer, New York.

Feature Article: Rapid spot imaging method

In optical imaging experiments, it is often advantageous to map the field of view and to converge the eyes without electrophysiological recording. We have developed a rapid spot imaging method that can be conducted rapidly and repeatedly throughout an experiment. Using small 0.2° - 0.5° spots, we can quickly map 1) the extent of the imaged field of view and 2) assess eye convergence to within 0.1° resolution.

Lu HD*, Chen G*, Ts'o DY, Roe AW (2008) A rapid topographic mapping and eye alignment method using optical imaging in Macaque visual cortex. Neuroimage, 44(3):636-46. *equal contributions.

Feature Article: 3D Maps in Visual Area V2

When we open our eyes, the 3D visual world is projected onto the 2D plane of our retina. Our brain reconstructs the third dimension (depth) by comparing inputs from the two eyes. But where in the brain is this third dimension calculated? To answer this question, we have used a high spatial resolution brain imaging method called optical imaging. We find that whereas primary
visual cortex (V1) contains a 2D map of visual space, the third dimension is mapped in the second visual area (V2). This suggests that 3D vision results from a combination of V1 and V2 activations. At right: Layer above is color-coded schematic of orientation map in V1 and V2. Peaks and valleys in V2 indicate maps for near to far in V2 thick stripes. Layer below indicates location of V1 region (light blue), V2 pale stripe (olive), V2 thin stripe (gray), and V2 thick stripe (cream).

Chen G, Lu HD, Roe AW (2008) A map of horizontal disparity in primate V2. Neuron, 58:442-450
Feature Article: Yin and Yang of color maps in the brain

Macaque monkey visual cortex (areas V1 and V2). Yin (right portion): optical image of V1 & V2 activation while monkey is viewing a color stimulus. Yang (left portion): cytochrome-oxidase (CO) stained brain slice of the imaged region. As shown in Lu and Roe 2008, color-activations in V1 (smaller patches) align with CO blobs in V1, while color-activations in V2 (larger patches) align with CO thin stripes in V2.

Lu HD, Roe AW (2008) Functional Organization of Color Domains in V1 and V2 of Macaque Monkey Revealed by Optical Imaging. Cereb Cortex 18(2).

Feature Article: Disparity Channels in Early Vision
Human beings and many other animals see the world with two eyes. However, each eye has a view which is slightly offset from the other. The brain has taken advantage of this offset, termed binocular disparity, to figure out distance and three dimensional depth information about the world, a capability called stereopsis. The last decade has seen a dramatic increase in our knowledge of the neural basis of stereopsis. New cortical areas have been found to represent binocular disparities, and the first causal links between neural activity and depth perception have been established. Equally exciting is the finding that experience affects how signals are channeled through different brain areas, a flexibility that may be crucial for learning, plasticity, and recovery of function.

Roe AW, Parker AJ, Born RT, DeAngelis GC (2007) Disparity channels in early vision: a mini-review. J Neurosci, 27:11820-11831.
Feature Article: How our brain fills gaps

A vase from China's Song dynasty demonstrates the use of very faint contrast borders to create the illusion of shading on a one-color background. The phenomenon is known as edge induction. The image of the vase is overlaid over the Cornsweet illusion, in which the left half of a rectangle divided in two looks lighter and the right area darker. Holding one's hand over the center of the image reveals that the left and the right are in fact the same color. The brain "fills in" the color on the left and the right in response to information from the middle border.

Hung CP, Ramsden RM, Roe AW (2007) A functional circuitry for edge-induced brightness perception. Nature Neurosci,/ /10:1185-1190.

See also http://www.vanderbilt.edu/news/releases/2007/8/20/
when-in-doubt-brain-relies-on-precise-timing-to-perceive-brightness
.


Feature article: The Power of Proximity

In Michelangelo's Creation of Adam (Sistine Chapel), God stretches out His right index to the first man. In a return gesture, Adam mirrors the movement, reaching out his own hand to meet the Creator's animating spark. Graphs on either side illustrate activations in somatosensory cortex in response to real and illusory digit tip stimulation.*


Chen LM, Turner G, Friedman RM, Gore JC, Roe AW, Avison MJ (2007) High resolution maps of real and illusory tactile activation in SI: intra-individual correlation with fMRI, optical imaging and electrophysiology. J Neurosci,/ /27(34):9181-9191.
Publications & Conferences
Laboratory Members
Web Links
Curriculum Vitae
Courses