Consequence of habitat specificity: a rising risk of habitat loss for endemic and sub-endemic woody species under climate change in the Hyrcanian ecoregion

Endemic species are more impacted by climate change than other taxa. However, assessing the vulnerability of endemics to these changes in some regions, such as the Hyrcanian forest, is limited, despite its importance for biodiversity and ecosystem function. To address the question of expected habitat shifts under climate change across the Hyrcanian ecoregion, we built an ensemble of species distribution models (SDM) under two emission scenarios (RCP 4.5 and RCP 8.5) for 15 endemic woody taxa. To identify the potential priority conservation areas, we also applied a spatial prioritization approach. Overall, our results suggest that the impacts of climate change are more severe on the eastern parts of the region (Golestan) and the Talysh Mountains (north-western Hyrcanian ecoregion) with over 85% and 34% loss of suitable habitats over the next 80 years. The central part of the Alborz Mountains (Mazandaran) and some areas in the Talysh Mountains could be potential climatic refugia under the future conditions for endemic taxa. The most prominent changes are expected for Ruscus hyrcanus, Gleditsia capsica, Acer velutinum, Frangula grandifolia, and Buxus hyrcana. The worrying predicted loss of suitable habitats for most studied taxa would dramatically affect the stability and resilience of forests, threatening thus biodiversity of the Hyrcanian ecoregion. We present the first estimation of the potential risks involved and provide useful support for regional climate-adaptation strategy, indicating potential conservation priority areas for maintaining and preserving its resources. Notably, only 13.4% of areas designated for conservation and management under climate change will be located within the current Hyrcanian protected areas, yet the majority of these areas are classified as low priority

SorCS2 facilitates release of endostatin from astrocytes and controls post-stroke angiogenesis

SorCS2 is an intracellular sorting receptor of the VPS10P domain receptor gene family recently implicated in oxidative stress response. Here, we interrogated the relevance of stress-related activities of SorCS2 in the brain by exploring its role in ischemic stroke in mouse models and in patients. Although primarily seen in neurons in the healthy brain, expression of SorCS2 was massively induced in astrocytes surrounding the ischemic core in mice following stroke. Post-stroke induction was likely a result of increased levels of transforming growth factor β1 in damaged brain tissue, inducing Sorcs2 gene transcription in astrocytes but not neurons. Induced astrocytic expression of SorCS2 was also seen in stroke patients, substantiating the clinical relevance of this observation. In astrocytes in vitro and in the mouse brain in vivo, SorCS2 specifically controlled release of endostatin, a factor linked to post-stroke angiogenesis. The ability of astrocytes to release endostatin acutely after stroke was lost in mice deficient for SorCS2, resulting in a blunted endostatin response which coincided with impaired vascularization of the ischemic brain. Our findings identified activated astrocytes as a source for endostatin in modulation of post-stroke angiogenesis, and the importance of the sorting receptor SorCS2 in this brain stress response