Figure-Ground Segregation and Brightness Perception at Illusory Contours: A Neuronal Model

Author(s):  
E. Peterhans ◽  
R. van der Zwan ◽  
B. Heider ◽  
F. Heitger
Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 66-66 ◽  
Author(s):  
F Heitger ◽  
E Peterhans

A previous model of visual cortical contour processing simulated the perception of illusory contours and the direction of figure and ground at such contours (Heitger and von der Heydt, 1993 Proceedings of International Conference on Computer Vision). This model was based on ‘complex type’ operators. Hence, it lacked representations of contrast polarity and could not account for brightness effects of illusory figures. Recently, we found that some neurons of area V2 in monkey visual cortex that signalled illusory contours were also sensitive to the figure — ground direction and contrast polarity at such contours. This allowed us to extend the previous scheme by incorporating the signals of even and odd symmetrical ‘simple type’ operators, particularly at the level of the ‘end-stopped’ operators which served the detection of the inducing elements of illusory figures (line ends, corners). To represent illusory contours, the signals of these operators were grouped with the use of fields of wide spatial support. Line ends and corners were handled differently in this process: at corners, signals parallel to the illusory contour were emphasised (para grouping), whereas at line ends signals orthogonal to the contour (ortho grouping) were emphasised. Further, ortho grouping included only end-stopped operators with even-symmetrical fields, para grouping only operators with odd-symmetrical fields. Thus, both processes contributed to the contrast polarity represented at illusory contours. Results of simulations showed that this model reproduces the shapes of illusory contours, their figure — ground direction, and contrast polarity. Hence, it can explain the selectivity of cortical neurons at such contours and the perceived brightness of illusory figures.


2020 ◽  
pp. 9-24
Author(s):  
Peter Bodrogi ◽  
Xue Guo ◽  
Tran Quoc Khanh

The brightness perception of a large (41°) uniform visual field was investigated in a visual psychophysical experiment. Subjects assessed the brightness of 20 light source spectra of different chromaticities at two luminance levels, Lv=267.6 cd/m2 and Lv=24.8 cd/m2. The resulting mean subjective brightness scale values were modelled by a combination of the signals of retinal mechanisms: S-cones, rods, intrinsically photosensitive retinal ganglion cells (ipRGCs) and the difference of the L-cone signal and the M-cone signal. A new quantity, “relative spectral blue content”, was also considered for modelling. This quantity was defined as “the spectral radiance of the light stimulus integrated with the range (380–520) nm, relative to luminance”. The “relative spectral blue content” model could describe the subjective brightness perception of the observers with reasonable accuracy.


2016 ◽  
Author(s):  
Daniele Quintella Mendes ◽  
Luís Alfredo V. Carvalho ◽  
Roseli S. Wedemann
Keyword(s):  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Chialin Cheng ◽  
Surya A. Reis ◽  
Emily T. Adams ◽  
Daniel M. Fass ◽  
Steven P. Angus ◽  
...  

AbstractMutations in MAPT (microtubule-associated protein tau) cause frontotemporal dementia (FTD). MAPT mutations are associated with abnormal tau phosphorylation levels and accumulation of misfolded tau protein that can propagate between neurons ultimately leading to cell death (tauopathy). Recently, a p.A152T tau variant was identified as a risk factor for FTD, Alzheimer's disease, and synucleinopathies. Here we used induced pluripotent stem cells (iPSC) from a patient carrying this p.A152T variant to create a robust, functional cellular assay system for probing pathophysiological tau accumulation and phosphorylation. Using stably transduced iPSC-derived neural progenitor cells engineered to enable inducible expression of the pro-neural transcription factor Neurogenin 2 (Ngn2), we generated disease-relevant, cortical-like glutamatergic neurons in a scalable, high-throughput screening compatible format. Utilizing automated confocal microscopy, and an advanced image-processing pipeline optimized for analysis of morphologically complex human neuronal cultures, we report quantitative, subcellular localization-specific effects of multiple kinase inhibitors on tau, including ones under clinical investigation not previously reported to affect tau phosphorylation. These results demonstrate the potential for using patient iPSC-derived ex vivo models of tauopathy as genetically accurate, disease-relevant systems to probe tau biochemistry and support the discovery of novel therapeutics for tauopathies.


2021 ◽  
Vol 3 (3) ◽  
Author(s):  
Alessandra Lucchetti ◽  
Mogens H. Jensen ◽  
Mathias L. Heltberg

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