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Walsh, W.

Publications and source records attributed to Walsh, W..

2 recordsLinked to original sources

Biological point-light displays scanning by the principal eyes of a jumping spider

The semi-rigid structure of bodies forces mobile animals to move in rhythmic patterns shared by all creatures with skeletons, exoskeletons, or limb connections. This pattern, known as biological motion, is instantly recognizable and conveys "animacy," even when body shape is removed and only a cloud of moving dots is shown. Indeed, motion alone is so informative that some animals can infer the original shape based on the dots concurrent activity. Jumping spiders, highly visual arthropods, divide motion detection and shape recognition between their four pairs of eyes. Previous studies found that they can distinguish biological from non-biological motion using only their motion-detecting anterior lateral eyes yet seemed unable to extract shape from motion. In this study, we examined how the anterior medial eyes of jumping spiders--which are used for shape recognition--respond to dot clouds depicting biological or non-biological motion. Using a custom eye tracker, we monitored retinal movements during presentation of static and moving stimuli. We found spiders change their retinal shifting pattern based on both the targets motion (biological or not) and implied structure (i.e., whether dots suggest a coherent shape). These results reveal that jumping spiders analyze motion with more complexity than previously thought, suggesting a deeper integration of motion and form processing within their minuscule, modular brains.

animal behavior and cognition↗

Mesoderm-Derived PDGFRA+ Cells Regulate the Emergence of Hematopoietic Stem Cells in the Dorsal Aorta

Mouse hematopoietic stem cells (HSCs) first emerge at embryonic day 10.5 (E10.5) on the ventral surface of the dorsal aorta, by endothelial-to-hematopoietic transition (EHT). We investigated whether cells with mesenchymal stem cell-like activity, which provide an essential niche for long-term HSCs (LT-HSCs) in the bone marrow, reside in the aorta- gonad-mesonephros (AGM) and contribute to the structural development of the dorsal aorta and EHT. Using transgenic mice, we demonstrate a lineage hierarchy for AGM stromal cells and traced the E10.5/E11.5 aortic endothelium and HSCs to mesoderm derived (Mesp1) PDGFRA+ stromal cells (Mesp1der PSCs). Mesp1der PSCs dominate the sub-endothelial and ventral stroma in the E10.5-E11.5 AGM but by E13.5 were replaced by neural crest (Wnt1) derived PDGFRA+ stromal cells (Wnt1der PSCs). Co-aggregating non-hemogenic embryonic and adult endothelial cells with Mesp1der PSCs but not with Wnt1der PSCs resulted in activation of a hematopoietic transcriptional program in endothelial cells accompanied by EHT and generation of LT-HSCs. Dose-dependent inhibition of PDGFRA signalling or BMP, WNT, NOTCH signalling interrupted this reprogramming event. This partnership between endothelial cells and AGM Mesp1der PSCs could potentially be harnessed to manufacture LT-HSCs from endothelium.

developmental biology↗