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Mechanisms underlying simultaneous brightness contrast: Early and innate.

ABSTRACT: In the phenomenon of simultaneous brightness contrast, two patches, one on a dark background and the other on a light one, appear to have different brightness despite being physically equi-luminant. Elucidating the phenomenon's underlying mechanisms is relevant for the larger question of how the visual system makes photometric judgments in images. Accounts over the past century have spanned low-, mid- and high-level visual processes, but a definitive resolution has not emerged. We present three studies that collectively demonstrate that the computations underlying this phenomenon are low-level, instantiated prior to binocular fusion, and available innately, without need for inferential learning via an individual's visual experience. In our first two studies, we find that strong brightness induction is obtained even when observers are unaware of any luminance differences in the neighborhoods of the probe patches. Results with dichoptic displays reveal that eye of origin, although not evident consciously, has a marked influence on the eventual brightness percept of the probe patches, thereby localizing brightness estimation to a site preceding binocular fusion. The third study uses conventional simultaneous brightness contrast displays, but an unusual group of participants: Congenitally blind children whom we were able to treat surgically. The results demonstrate an immediate susceptibility to the simultaneous brightness illusion after sight onset. Together, these data strongly constrain the search for mechanisms underlying a fundamental brightness phenomenon.

SUBMITTER: Sinha P

PROVIDER: S-EPMC7310601 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:Preeclampsia is a complex cardiovascular disorder of pregnancy with underlying multifactorial pathogeneses; however, its etiology is not fully understood. It is characterized by the new onset of maternal hypertension after 20 weeks of gestation, accompanied by proteinuria, maternal organ damage, and/or uteroplacental dysfunction. Preeclampsia can be subdivided into early- and late-onset phenotypes (EOPE and LOPE), diagnosed before 34 weeks or from 34 weeks of gestation, respectively. Impaired placental development in early pregnancy and subsequent growth restriction is often associated with EOPE, while LOPE is associated with maternal endothelial dysfunction. The innate immune system plays an essential role in normal progression of physiological pregnancy and fetal development. However, inappropriate or excessive activation of this system can lead to placental dysfunction or poor maternal vascular adaptation and contribute to the development of preeclampsia. This review aims to comprehensively outline the mechanisms of key innate immune cells including macrophages, neutrophils, natural killer (NK) cells, and innate B1 cells, in normal physiological pregnancy, EOPE and LOPE. The roles of the complement system, syncytiotrophoblast extracellular vesicles and mesenchymal stem cells (MSCs) are also discussed in the context of innate immune system regulation and preeclampsia. The outlined molecular mechanisms, which represent potential therapeutic targets, and associated emerging treatments, are evaluated as treatments for preeclampsia. Therefore, by addressing the current understanding of innate immunity in the pathogenesis of EOPE and LOPE, this review will contribute to the body of research that could lead to the development of better diagnosis, prevention, and treatment strategies. Importantly, it will delineate the differences in the mechanisms of the innate immune system in two different types of preeclampsia, which is necessary for a more personalized approach to the monitoring and treatment of affected women.

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Mechanisms underlying simultaneous brightness contrast: Early and innate.

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