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Cowen, M.

Publications and source records attributed to Cowen, M..

2 recordsLinked to original sources

Spatial overlap and phenotypic similarity predict hybridisation in birds

Hybridisation is widespread in birds and has important eco-evolutionary implications. Historically, much research has focused on the consequences of hybridisation. To date, however, far less attention has been paid to the causes of hybridisation and, in particular, why particular pairs of species form hybrids. Using large-scale comparative analyses, we find that similarity in plumage, vocalisations, and morphometric traits, as well as evolutionary relatedness, drive hybridisation in North American and European birds. In passerines, the avian order including songbirds, similarity in vocalisations and morphology are the key phenotypic predictors of hybridisation, whereas in non-passerines, species pairs with similar plumage and morphology are more likely to hybridise. We also find that the likelihood of hybrid formation increases with the magnitude of range and habitat overlap, demonstrating that hybridisation is not just a product of occasional contact between closely related species. Our findings have important conservation implications in this age of rapid anthropogenic change and species reassembly.

evolutionary biology↗

Retroviral Infection of Human Neurospheres and Use of Stem Cell EVs to Repair Cellular Damage

HIV-1 remains an incurable infection that is associated with substantial economic and epidemiologic impacts. HIV-associated neurocognitive disorders (HAND) are commonly linked with HIV-1 infection; despite the development of combination antiretroviral therapy (cART), HAND is still reported to affect at least 50% of HIV-1 infected individuals. It is believed that the over-amplification of inflammatory pathways, along with release of toxic viral proteins from infected cells, are primarily responsible for the neurological damage that is observed in HAND; however, the underlying mechanisms are not well-defined. Therefore, there is an unmet need to develop more physiologically relevant and reliable platforms for studying these pathologies. In recent years, neurospheres derived from induced pluripotent stem cells (iPSCs) have been utilized to model the effects of different neurotropic viruses. Here, we report the generation of neurospheres from iPSC-derived neural progenitor cells (NPCs) and we show that these cultures are permissive to retroviral (e.g. HIV-1, HTLV-1) replication. In addition, we also examine the potential effects of stem cell derived extracellular vesicles (EVs) on HIV-1 damaged cells as there is abundant literature supporting the reparative and regenerative properties of stem cell EVs in the context of various CNS pathologies. Consistent with the literature, our data suggests that stem cell EVs may modulate neuroprotective and anti-inflammatory properties in damaged cells. Collectively, this study demonstrates the feasibility of NPC-derived neurospheres for modeling HIV-1 infection and, subsequently, highlights the potential of stem cell EVs for rescuing cellular damage induced by HIV-1 infection.

cell biology↗