Literature DB >> 3657960

Endstopped neurons in the visual cortex as a substrate for calculating curvature.

A Dobbins1, S W Zucker, M S Cynader.   

Abstract

Neurons in the visual cortex typically respond selectively to the orientation, and velocity and direction of movement, of moving-bar stimuli. These responses are generally thought to provide information about the orientation and position of lines and edges in the visual field. Some cells are also endstopped, that is selective for bars of specific lengths. Hubel and Wiesel first observed that endstopped hypercomplex cells could respond to curved stimuli and suggested they might be involved in detection of curvature, but the exact relationship between endstopping and curvature has never been determined. We present here a mathematical model relating endstopping to curvature in which the difference in response of two simple cells gives rise to endstopping and varies in proportion to curvature. We also provide physiological evidence that endstopped cells in area 17 of the cat visual cortex are selective for curvature, whereas non-endstopped cells are not, and that some are selective for the sign of curvature. The prevailing view of edge and curve determination is that orientations are selected locally by the class of simple cortical cells and then integrated to form global curves. We have developed a computational theory of orientation selection which shows that measurements of orientation obtained by simple cells are not sufficient because there will be strong, incorrect responses from cells whose receptive fields (RFs) span distinct curves (Fig. 1). If estimates of curvature are available, however, these inappropriate responses can be eliminated. Curvature provides the key to structuring the network that underlies our theory and distinguishes it from previous lateral inhibition schemes.

Mesh:

Year:  1987        PMID: 3657960     DOI: 10.1038/329438a0

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  41 in total

1.  Asymmetric suppression outside the classical receptive field of the visual cortex.

Authors:  G A Walker; I Ohzawa; R D Freeman
Journal:  J Neurosci       Date:  1999-12-01       Impact factor: 6.167

2.  Shape tuning in macaque inferior temporal cortex.

Authors:  Greet Kayaert; Irving Biederman; Rufin Vogels
Journal:  J Neurosci       Date:  2003-04-01       Impact factor: 6.167

3.  On the computational architecture of the neocortex. II. The role of cortico-cortical loops.

Authors:  D Mumford
Journal:  Biol Cybern       Date:  1992       Impact factor: 2.086

4.  Curvature processing dynamics in macaque area V4.

Authors:  Jeffrey M Yau; Anitha Pasupathy; Scott L Brincat; Charles E Connor
Journal:  Cereb Cortex       Date:  2012-01-31       Impact factor: 5.357

5.  End stopping in V1 is sensitive to contrast.

Authors:  Arash Yazdanbakhsh; Margaret S Livingstone
Journal:  Nat Neurosci       Date:  2006-04-23       Impact factor: 24.884

6.  Visual saliency and texture segregation without feature gradient.

Authors:  Ohad Ben-Shahar
Journal:  Proc Natl Acad Sci U S A       Date:  2006-10-09       Impact factor: 11.205

7.  Direction selectivity in V1 of alert monkeys: evidence for parallel pathways for motion processing.

Authors:  Moshe Gur; D Max Snodderly
Journal:  J Physiol       Date:  2007-10-11       Impact factor: 5.182

8.  Selective mechanisms for simple contours revealed by compound adaptation.

Authors:  Sarah Hancock; Jonathan W Peirce
Journal:  J Vis       Date:  2008-06-03       Impact factor: 2.240

9.  Curvature domains in V4 of macaque monkey.

Authors:  Jia Ming Hu; Xue Mei Song; Qiannan Wang; Anna Wang Roe
Journal:  Elife       Date:  2020-11-19       Impact factor: 8.140

10.  Curvature-processing domains in primate V4.

Authors:  Rendong Tang; Qianling Song; Ying Li; Rui Zhang; Xingya Cai; Haidong D Lu
Journal:  Elife       Date:  2020-11-19       Impact factor: 8.140

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