Artificial retina chips for image processing

Artificial retina chips which can simultaneously sense and process real world images are described. The comparison between artificial retinal systems and conventional image processing systems is described. Variable sensitivity photodetection, which is an essential technology for the artificial retina chips, is introduced in detail. The concept, structure, fundamental performance, operating principle, and processing functions for the fabricated artificial retinal chips are described. Applications including interactive games by gesture-input are also introduced. This work was presented, in part, at the International Symposium on Artificial Life and Robotics, Oita, Japan, February 18–20, 1996.     

Neural architecture for robotic vision sensor that discounts uneven illumination in a manufacturing environment

Computer vision algorithms for inspection or pick-and-place operations often depend on spatially uniform illumination of a workplace. This necessitates expensive lighting fixtures. To discount effects of uneven illumination we designed and tested a neural network that can adaptively control light sensitivity at the photosensor level. Our neural network architecture consists of multiple layers with hexagonally arranged nodes. All nodes have partially overlapping receptive fields of different spatial frequencies. Feedforward connections are excitatory while feedback pathways subserve lateral inhibition. The outputs of these nodes are combined so as to maximize the signal-to-noise ratio while constantly resetting thresholds to maintain high sensitivity. Our connectionist architecture can account for many characteristics attributed to the lightness constancy phenomenon observed in biological systems. The results suggest that our module maintains high sensitivity over the whole domain of intensities without interfering with transmission of visual information embedded in spatial discontinuities of intensity.     

Differential Action of Connexin Hemichannel and Pannexin Channel Therapeutics for Potential Treatment of Retinal Diseases

Dysregulation of retinal function in the early stages of light-induced retinal degeneration involves pannexins and connexins. These two types of proteins may contribute to channels that release ATP, leading to activation of the inflammasome pathway, spread of inflammation and retinal dysfunction. However, the effect of pannexin channel block alone or block of both pannexin channels and connexin hemichannels in parallel on retinal activity in vivo is unknown. In this study, the pannexin channel blocker probenecid and the connexin hemichannel blocker tonabersat were used in the light-damaged rat retina. Retinal function was evaluated using electroretinography (ERG), retinal structure was analyzed using optical coherence tomography (OCT) imaging and the tissue response to light-induced injury was assessed immunohistochemically with antibodies against glial fibrillary acidic protein (GFAP), Ionized calcium binding adaptor molecule 1 (Iba-1) and Connexin43 (Cx43). Probenecid did not further enhance the therapeutic effect of connexin hemichannel block in this model, but on its own improved activity of certain inner retina neurons. The therapeutic benefit of blocking connexin hemichannels was further evaluated by comparing these data against results from our previously published studies that also used the light-damaged rat retina model. The analysis showed that treatment with tonabersat alone was better than probenecid alone at restoring retinal function in the light-damaged retina model. The results assist in the interpretation of the differential action of connexin hemichannel and pannexin channel therapeutics for potential treatment of retinal diseases.     

基于视觉感知机制的织物疵点轮廓检测

针对传统人工织物疵点检测存在的误检及低效等问题,提出了一种基于视觉感知机制的自适应织物疵点轮廓检测方法.首先,模拟视觉系统中视网膜感受野对视觉信息的处理机制对织物疵点图像进行滤波及疵点增强;其次,依据初级视皮层(V1)区对视觉信息响应的方向选择性机制构建织物疵点图像边缘检测模型,实现对织物疵点图像的边缘检测.最后,采用自适应阈值选择的方法对检测到的边缘进行二次处理,获得织物图像疵点的轮廓.为验证本文方法的有效性和准确性,对4类织物疵点图像进行测试,并定性和定量两方面进行比较分析,结果表明文中提出的方法能够较好地检测出织物疵点轮廓信息,不仅可以得到质量较高的织物疵点轮廓图像,而且在整个检测过程中能够自适应的选择参数,避免受人的主观因素影响,具有实际的应用价值.     

基于自适应阈值和区域生长的SD-OCT糖网图像亮斑分割

硬性渗出是糖尿病性视网膜病变的一个比较显著的症状,频域光学相干断层视网膜图像中的高信号亮斑与渗出有着密切的联系。为了研究渗出与病变的关系,有必要找到一种提取亮斑的方法。但是,目前关于糖网图像亮斑提取的研究还非常少。首先运用层分割算法限制亮斑所在区域,然后采用自适应阈值法确定种子集合,最后使用基于人类视觉特性的区域生长方法提取出亮斑。实验结果表明,本方法可以较准确地分割出糖网图像中的亮斑。     

Development of an image-based model for capillary vasculature of retina

The paper presents a method of development of a detailed network model to represent retinal capillary vasculature. The capillary model is a circular mesh consisting of concentric rings with an increasing diameter. Each of the rings has uniformly distributed bifurcation nodes to represent capillary vessels. The model is customized using the data that has been measured from confocal microscopic images of a mouse retina. The capillary model developed can be connected to networks of larger vessels of the vasculature such as arterial and venous networks to form a complete model of the retinal network. A method to automate such interface connections between capillary and other vascular networks using connecting vessels (i.e., pre-capillary and post-capillary) is also presented in the paper. Such a detailed image-based capillary model together with the arterial and venular networks can be used for various circulation simulations to obtain accurate information on hemodynamic quantities such as the spatial distribution of pressure and flow in the vasculature for both physiological and pathological conditions. The method presented for the development of the capillary model can also be adopted for vasculatures of other organs.     

The Stiles–Crawford Effect: spot-size ratio departure in retinitis pigmentosa

The Stiles–Crawford effect of the first kind is the retina’s compensative response to loss of luminance efficiency for oblique stimulation manifested as the spot-size ratio departure from the perfect power coupling for a normal human eye. In a retinitis pigmentosa eye (RP), the normal cone photoreceptor morphology is affected due to foveal cone loss and disrupted cone mosaic spatial arrangement with reduction in directional sensitivity. We show that the flattened Stiles–Crawford function (SCF) in a RP eye is due to a different spot-size ratio departure profile, that is, for the same loss of luminance efficiency, a RP eye has a smaller departure from perfect power coupling compared to a normal eye. Again, the difference in spot-size ratio departure increases from the centre towards the periphery, having zero value for axial entry and maximum value for maximum peripheral entry indicating dispersal of photoreceptor alignment which prevents the retina to go for a bigger compensative response as it lacks both in number and appropriate cone morphology to tackle the loss of luminance efficiency for oblique stimulation. The slope of departure profile also testifies to the flattened SCF for a RP eye. Moreover, the discrepancy in spot-size ratio departure between a normal and a RP eye is shown to have a direct bearing on the Stiles–Crawford diminution of visibility.     

The Rise of Retinal Organoids for Vision Research

Retinal degenerative diseases lead to irreversible blindness. Decades of research into the cellular and molecular mechanisms of retinal diseases, using either animal models or human cell-derived 2D systems, facilitated the development of several therapeutic interventions. Recently, human stem cell-derived 3D retinal organoids have been developed. These self-organizing 3D organ systems have shown to recapitulate the in vivo human retinogenesis resulting in morphological and functionally similar retinal cell types in vitro. In less than a decade, retinal organoids have assisted in modeling several retinal diseases that were rather difficult to mimic in rodent models. Retinal organoids are also considered as a photoreceptor source for cell transplantation therapies to counteract blindness. Here, we highlight the development and field’s improvements of retinal organoids and discuss their application aspects as human disease models, pharmaceutical testbeds, and cell sources for transplantations.