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J Neurophysiol 102: 2603-2615, 2009. First published July 1, 2009; doi:10.1152/jn.91255.2008
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RESEARCH-ARTICLE

Organization of Hue Selectivity in Macaque V2 Thin Stripes

Heejin Lim1,*, Yi Wang1,2,*, Youping Xiao1,3,*, Ming Hu2 and Daniel J. Felleman1

1Department of Neurobiology and Anatomy, University of Texas Medical School–Houston, Houston, Texas; 2State Key Laboratory of Brain and Cognitive Sciences, Institute of Biophysics, Chinese Academy of Sciences, Beijing, China; and 3Department of Neuroscience, Mount Sinai School of Medicine, New York, New York

Submitted 25 November 2008; accepted in final form 28 June 2009

ABSTRACT

V2 has long been recognized to contain functionally distinguishable compartments that are correlated with the stripelike pattern of cytochrome oxidase activity. Early electrophysiological studies suggested that color, direction/disparity, and orientation selectivity were largely segregated in the thin, thick, and interstripes, respectively. Subsequent studies revealed a greater degree of homogeneity in the distribution of response properties across stripes, yet color-selective cells were still found to be most prevalent in the thin stripes. Optical recording studies have demonstrated that thin stripes contain both color-preferring and luminance-preferring modules. These thin stripe color-preferring modules contain spatially organized hue maps, whereas the luminance-preferring modules contain spatially organized luminance-change maps. In this study, the neuronal basis of these hue maps was determined by characterizing the selectivity of neurons for isoluminant hues in multiple penetrations within previously characterized V2 thin stripe hue maps. The results indicate that neurons within the superficial layers of V2 thin stripe hue maps are organized into columns whose aggregated hue selectivity is closely related to the hue selectivity of the optically defined hue maps. These data suggest that thin stripes contain hue maps not simply because of their moderate percentage of hue-selective neurons, but because of the columnar and tangential organization of hue selectivity.


Address for reprint requests and other correspondence: D. J. Felleman, Department of Neurobiology and Anatomy, University of Texas Medical School–Houston, 6431 Fannin St., Houston, TX 77030 (E-mail: daniel.felleman{at}uth.tmc.edu).







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