A neural circuit for spatial orientation derived from brain lesions.

There is disagreement regarding the major components of the brain network supporting spatial cognition. To address this issue, we applied a lesion mapping approach to the clinical phenomenon of topographical disorientation. Topographical disorientation is the inability to maintain accurate knowledge about the physical environment and use it for navigation. A review of published topographical disorientation cases identified 65 different lesion sites. Our lesion mapping analysis yielded a topographical disorientation brain map encompassing the classic regions of the navigation network: medial parietal, medial temporal, and temporo-parietal cortices. We also identified a ventromedial region of the prefrontal cortex, which has been absent from prior descriptions of this network. Moreover, we revealed that the regions mapped are correlated with the Default Mode Network sub-network C. Taken together, this study provides causal evidence for the distribution of the spatial cognitive system, demarking the major components and identifying novel regions.

Brain System for Social Categorization by Narrative Roles.

The cognitive system applies categorical thinking to facilitate perception of the rich environment around us. In person cognition, research has focused on the roles of gender, race, age, or appearance in social categorical thinking. Here we investigated how narrative roles, as portrayed by different cinematic characters, are categorized in the neurocognitive system. Under functional MRI, 17 human participants (7 females) were asked to make different judgments regarding personality traits of 16 renowned cinematic characters representing four roles: hero, sidekick, mentor, and villain. Classification analysis showed a brain network, comprising the dorsal medial prefrontal cortex, the precuneus and the temporoparietal junction bilaterally, and the left occipital face area (OFA), to discriminate among the four roles. No such classification was found between other individual attributes including age or the associated film. Moreover, regions overlapping the default mode network (DMN) were found to better discriminate between roles, rather than the individual characters, while the OFA was found to better discriminate between individuals. These results demonstrate the inherent role of roles in person cognition, and suggest an intimate relation between roles categorization and self-referential activity.SIGNIFICANCE STATEMENT Social categorization, the assignment of different people in our social network to subgroups, is a powerful strategy in social cognition. How is this managed by the brain? We provide evidence that different characters from different stories, representing similar roles in their corresponding narrative, elicit similar brain activation patterns, as revealed by functional MRI. Unlike previous studies of social categorization, these brain activations were similar to those elicited by social cognition rather than face processing, and included regions at the prefrontal cortex, the precuneus, and the temporoparietal junction. The identified brain network significantly overlapped the default mode network. We suggest that social categorization by roles is fundamental to the cognitive system, relying on brain regions related to social cognition.

Zika Virus Infects Early- and Midgestation Human Maternal Decidual Tissues, Inducing Distinct Innate Tissue Responses in the Maternal-Fetal Interface.

Zika virus (ZIKV) has emerged as a cause of congenital brain anomalies and a range of placenta-related abnormalities, highlighting the need to unveil the modes of maternal-fetal transmission. The most likely route of vertical ZIKV transmission is via the placenta. The earliest events of ZIKV transmission in the maternal decidua, representing the maternal uterine aspect of the chimeric placenta, have remained unexplored. Here, we show that ZIKV replicates in first-trimester human maternal-decidual tissues grown ex vivo as three-dimensional (3D) organ cultures. An efficient viral spread in the decidual tissues was demonstrated by the rapid upsurge and continued increase of tissue-associated ZIKV load and titers of infectious cell-free virus progeny, released from the infected tissues. Notably, maternal decidual tissues obtained at midgestation remained similarly susceptible to ZIKV, whereas fetus-derived chorionic villi demonstrated reduced ZIKV replication with increasing gestational age. A genome-wide transcriptome analysis revealed that ZIKV substantially upregulated the decidual tissue innate immune responses. Further comparison of the innate tissue response patterns following parallel infections with ZIKV and human cytomegalovirus (HCMV) revealed that unlike HCMV, ZIKV did not induce immune cell activation or trafficking responses in the maternal-fetal interface but rather upregulated placental apoptosis and cell death molecular functions. The data identify the maternal uterine aspect of the human placenta as a likely site of ZIKV transmission to the fetus and further reveal distinct patterns of innate tissue responses to ZIKV. Our unique experimental model and findings could further serve to study the initial stages of congenital ZIKV transmission and pathogenesis and evaluate the effect of new therapeutic interventions. IMPORTANCE: In view of the rapid spread of the current ZIKV epidemic and the severe manifestations of congenital ZIKV infection, it is crucial to learn the fundamental mechanisms of viral transmission from the mother to the fetus. Our studies of ZIKV infection in the authentic tissues of the human maternal-fetal interface unveil a route of transmission whereby virus originating from the mother could reach the fetal compartment via efficient replication within the maternal decidual aspect of the placenta, coinhabited by maternal and fetal cells. The identified distinct placental tissue innate immune responses and damage pathways could provide a mechanistic basis for some of the placental developmental abnormalities associated with ZIKV infection. The findings in the unique model of the human decidua should pave the way to future studies examining the interaction of ZIKV with decidual immune cells and to evaluation of therapeutic interventions aimed at the earliest stages of transmission.