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Recalde, J.

Publications and source records attributed to Recalde, J..

3 recordsLinked to original sources

Unifying spatial and episodic representations in the hippocampus through flexible memory use

A key question in neuroscience is why the hippocampus is essential for episodic memory in humans, while dominantly exhibiting spatial representations in a number of other species. Some accounts suggest that spatial representation is the primary hippocampal function. Here, we propose that the primary function is storing and retrieving episodic memories, and spatial representations emerge due to this memory function. To demonstrate this, we adopt a computational model that autonomously learns to store information in memory and retrieve it to solve a variety of tasks. In memory tasks, the model develops associations and categorical representations akin to concept cells. In navigation tasks, the model forms representations of the spatial structure, performs geometric computations, and even learns representations of unique events similar to recently discovered barcodes. Our model predicts that the hippocampus represents any task-relevant variable, if the animal learns the task, suggesting that space is not special for the hippocampus.

neuroscience↗

A role for Myosin in triggering and executing amnioserosa cell delaminations during dorsal closure.

The remodeling of epithelial tissues is a critical process in morphogenesis, often involving the apoptotic removal of individual cells while preserving tissue integrity. In Drosophila, the amnioserosa--a highly dynamic extra-embryonic tissue--undergoes extensive remodeling, culminating in its complete elimination at the end of dorsal closure. While apoptotic cell delaminations in the amnioserosa have been proposed to contribute to dorsal closure, the cellular mechanisms underlying this process remain poorly understood. In this study, we have investigated actomyosin dynamics during cell delaminations and analyzed the consequences of perturbing non-muscle Myosin activity globally in the entire tissue as well as locally in groups of cells. We found that Myosin plays an essential role in both triggering and executing cell delaminations, with high Myosin contractility promoting cell delamination via caspase activation. Additionally, our results suggest that cell delaminations are governed by both cell-autonomous Myosin dynamics and mechanical cues from the tissue environment. Together, these findings provide new insights into the regulation of epithelial cell removal and the complex interplay between apoptotic and mechanical signals during tissue remodeling.

developmental biology↗

Opposite patterns of association of TWIST1 expression with patient survival in SHH and Group 4 medulloblastoma

PurposeTwist1 is a transcription factor that regulates embryonic development, stemness, and differentiation, and can also stimulate initiation of tumorigenesis in peripheral solid cancers. However, its role in central nervous system tumors, including medulloblastoma (MB), the main type of malignant brain cancer that afflicts children, remains poorly understood. Here, we examined expression of Twist1, and its potential significance in prognosis, in different histological variants and molecular subgroups of MB. MethodsGene expression data for TWIST1 and corresponding overall survival (OS) of patients was analyzed in 612 MB samples using a previously described dataset. A cross-sectional analysis of Twist1 protein content in 24 MB tumor samples from patients was carried out by immunohistochemistry. ResultsTWIST1 transcript levels were higher in classic MB compared to desmoplastic tumors. Within samples with classic histology, higher TWIST1 expression was associated with a longer OS. Tumors in the SHH subgroup had lower TWIST1 expression compared to all other subgroups, and Group 4 showed lower expression than WNT tumors. In Group 4 MB, higher TWIST1 levels were associated with shorter OS, whereas patients with SHH tumors and higher TWIST1 levels showed longer OS. Twist1 protein was detectable in part of classic and LCA MB tumors belonging to the SHH, WNT or Group 3/4 subgroups. ConclusionWe found opposite patterns of association between TWST1 and patient survival in Group 4 and SHH MB subgroups. Our results highlight the importance of stratifying tumors by molecular subgroup and histological classification when exploring novel potential biomarkers and therapeutic targets in MB.

cancer biology↗