Topographic representation of visually evoked emotional experiences in the human cerebral cortex.

Affective neuroscience seeks to uncover the neural underpinnings of emotions that humans experience. However, it remains unclear whether an affective space underlies the discrete emotion categories in the human brain, and how it relates to the hypothesized affective dimensions. To address this question, we developed a voxel-wise encoding model to investigate the cortical organization of human emotions. Results revealed that the distributed emotion representations are constructed through a fundamental affective space. We further compared each dimension of this space to 14 hypothesized affective dimensions, and found that many affective dimensions are captured by the fundamental affective space. Our results suggest that emotional experiences are represented by broadly spatial overlapping cortical patterns and form smooth gradients across large areas of the cortex. This finding reveals the specific structure of the affective space and its relationship to hypothesized affective dimensions, while highlighting the distributed nature of emotional representations in the cortex.

High-dimensional topographic organization of visual features in the primate temporal lobe.

The inferotemporal cortex supports our supreme object recognition ability. Numerous studies have been conducted to elucidate the functional organization of this brain area, but there are still important questions that remain unanswered, including how this organization differs between humans and non-human primates. Here, we use deep neural networks trained on object categorization to construct a 25-dimensional space of visual features, and systematically measure the spatial organization of feature preference in both male monkey brains and human brains using fMRI. These feature maps allow us to predict the selectivity of a previously unknown region in monkey brains, which is corroborated by additional fMRI and electrophysiology experiments. These maps also enable quantitative analyses of the topographic organization of the temporal lobe, demonstrating the existence of a pair of orthogonal gradients that differ in spatial scale and revealing significant differences in the functional organization of high-level visual areas between monkey and human brains.

Retinoid X Receptor α Regulates DHA-Dependent Spinogenesis and Functional Synapse Formation In Vivo.

Coordinated intracellular and extracellular signaling is critical to synapse development and functional neural circuit wiring. Here, we report that unesterified docosahexaenoic acid (DHA) regulates functional synapse formation in vivo via retinoid X receptor α (Rxra) signaling. Using Rxra conditional knockout (cKO) mice and virus-mediated transient gene expression, we show that endogenous Rxra plays important roles in regulating spinogenesis and excitatory synaptic transmission in cortical pyramidal neurons. We further show that the effects of RXRA are mediated through its DNA-binding domain in a cell-autonomous and reversible manner. Moreover, unesterified DHA increases spine formation and excitatory synaptic transmission in vivo in an Rxra-dependent fashion. Rxra cKO mice generally behave normally but show deficits in behavior tasks associated with social memory. Together, these results demonstrate that unesterified DHA signals through RXRA to regulate spinogenesis and functional synapse formation, providing insight into the mechanism through which DHA promotes brain development and cognitive function.