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Urban landscapes have a negative impact on bird species diversity, yet particular species thrive in urban communities. Like many other corvids, the Korean magpie is a successful colonizer of urban environments. On the semiurban campus of Seoul National University in Korea, we investigated whether magpies adjust territory size with building area and secondarily, whether they use vegetation and artificial components of their territory as indicators of prey density. We measured territorial areas and divided these into vegetation and artificial areas, distinguishing building area as a separate feature. We sampled prey density on each territory during the nestling stage. Territory size increased with the square root of building area (SRBA). As the length of building perimeter also increases with SRBA, we conclude that territory size was proportional to building perimeter. Prey density decreased with SRBA indicating that buildings had a negative impact on prey. Breeding success was also negatively related to SRBA. We suggest that magpies adjusted territory size according to the length of building perimeter due to a decline in prey density. As prey density declined, artificial pavement area was added to include open trash bins, which increase the availability of anthropogenic refuse such as discarded food. Vegetation area declined as prey density increased, but changes in vegetation area were minor and had little impact on prey availability measured at ground level. Structural cues were not used to adjust vegetation area, and artificial structural cues were not used to adjust territorial size over direct monitoring of prey density.
Investigations of stem cell therapy for neurological disorders have primarily focused on the grafted cells’ effects within the local brain tissue. Despite mounting evidence of a massive peripheral inflammatory response accompanying stroke, the ability of intracerebrally transplanted cells to migrate to the periphery and sequester systemic inflammation remains unexplored. We previously reported that intravenously transplanted human bone marrow stem cells (hBMSCs) preferentially migrate to spleen, subsequently abrogating chronic inflammation in stroke. Here, we tested the hypothesis that intracerebrally transplanted stem cells in the brain of adult rats subjected to experimental stroke can migrate to the spleen, a vital organ that confers peripheral inflammation after stroke. Immunofluorescence microscopy revealed stem cells engrafted in the brain, but interestingly a specialized band of stem of cells homed to the spleen via lymphatic vessels, seemingly propelled by inflammatory signals. Mechanism-based in vitro studies using hBMSCs co-cultured with lymphatic endothelial cells or microglia, and treated with TNF-alpha further implicated the key role of the lymphatic system in directing stem cell migration and in dampening inflammation. Altogether, the results suggest a robust therapeutic outcome in stroke can be achieved by targeting the systemic inflammatory response. This study is the first to demonstrate brain‑to‑periphery migration of stem cells, advancing the novel concept of harnessing the lymphatic system in mobilizing stem cells to sequester peripheral inflammation as a brain repair strategy. FINANCIAL SUPPORT: CVB is supported by the National Institutes of Health.
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