56 research outputs found
The subsurface habitability of small, icy exomoons
Context. Assuming our Solar System as typical, exomoons may outnumber exoplanets. If their habitability fraction is similar, they would thus constitute the largest portion of habitable real estate in the Universe. Icy moons in our Solar System, such as Europa and Enceladus, have already been shown to possess liquid water, a prerequisite for life on Earth. Aims: We intend to investigate under what thermal and orbital circumstances small, icy moons may sustain subsurface oceans and thus be "subsurface habitable". We pay specific attention to tidal heating, which may keep a moon liquid far beyond the conservative habitable zone. Methods: We made use of a phenomenological approach to tidal heating. We computed the orbit averaged flux from both stellar and planetary (both thermal and reflected stellar) illumination. We then calculated subsurface temperatures depending on illumination and thermal conduction to the surface through the ice shell and an insulating layer of regolith. We adopted a conduction only model, ignoring volcanism and ice shell convection as an outlet for internal heat. In doing so, we determined at which depth, if any, ice melts and a subsurface ocean forms. Results: We find an analytical expression between the moon's physical and orbital characteristics and the melting depth. Since this expression directly relates icy moon observables to the melting depth, it allows us to swiftly put an upper limit on the melting depth for any given moon. We reproduce the existence of Enceladus' subsurface ocean; we also find that the two largest moons of Uranus (Titania and Oberon) could well sustain them. Our model predicts that Rhea does not have liquid water. Conclusions: Habitable exomoon environments may be found across an exoplanetary system, largely irrespective of the distance to the host star. Small, icy subsurface habitable moons may exist anywhere beyond the snow line. This may, in future observations, expand the search area for extraterrestrial habitable environments beyond the circumstellar habitable zone
Identification of parathyroid hormone-related protein-derived peptides immunogenic in human histocompatibility leukocyte antigen-A24+ prostate cancer patients
Vaccination of recurrent glioma patients with tumour lysate-pulsed dendritic cells elicits immune responses: results of a clinical phase I/II trial
Decidual-Secreted Factors Alter Invasive Trophoblast Membrane and Secreted Proteins Implying a Role for Decidual Cell Regulation of Placentation
Inadequate or inappropriate implantation and placentation during the establishment of human pregnancy is thought to lead to first trimester miscarriage, placental insufficiency and other obstetric complications. To create the placental blood supply, specialized cells, the ‘extravillous trophoblast’ (EVT) invade through the differentiated uterine endometrium (the decidua) to engraft and remodel uterine spiral arteries. We hypothesized that decidual factors would regulate EVT function by altering the production of EVT membrane and secreted factors. We used a proteomics approach to identify EVT membrane and secreted proteins regulated by decidual cell factors. Human endometrial stromal cells were decidualized in vitro by treatment with estradiol (10−8 M), medroxyprogesterone acetate (10−7 M) and cAMP (0.5 mM) for 14 days. Conditioned media (CM) was collected on day 2 (non-decidualized CM) and 14 (decidualized CM) of treatment. Isolated primary EVT cultured on Matrigel™ were treated with media control, non-decidualized or decidualized CM for 16 h. EVT CM was fractionated for proteins <30 kDa using size-exclusion affinity nanoparticles (SEAN) before trypsin digestion and HPLC-MS/MS. 43 proteins produced by EVT were identified; 14 not previously known to be expressed in the placenta and 12 which had previously been associated with diseases of pregnancy including preeclampsia. Profilin 1, lysosome associated membrane glycoprotein 1 (LAMP1), dipeptidyl peptidase 1 (DPP1/cathepsin C) and annexin A2 expression by interstitial EVT in vivo was validated by immunhistochemistry. Decidual CM regulation in vitro was validated by western blotting: decidualized CM upregulated profilin 1 in EVT CM and non-decidualized CM upregulated annexin A2 in EVT CM and pro-DPP1 in EVT cell lysate. Here, non-decidualized factors induced protease expression by EVT suggesting that non-decidualized factors may induce a pro-inflammatory cascade. Preeclampsia is a pro-inflammatory condition. Overall, we have demonstrated the potential of a proteomics approach to identify novel proteins expressed by EVT and to uncover the mechanisms leading to disease states
MicroRNA Dysregulation in the Spinal Cord following Traumatic Injury
Spinal cord injury (SCI) triggers a multitude of pathophysiological events that are tightly regulated by the expression levels of specific genes. Recent studies suggest that changes in gene expression following neural injury can result from the dysregulation of microRNAs, short non-coding RNA molecules that repress the translation of target mRNA. To understand the mechanisms underlying gene alterations following SCI, we analyzed the microRNA expression patterns at different time points following rat spinal cord injury
Clinical correlates of grey matter pathology in multiple sclerosis
Traditionally, multiple sclerosis has been viewed as a disease predominantly affecting white matter. However, this view has lately been subject to numerous changes, as new evidence of anatomical and histological changes as well as of molecular targets within the grey matter has arisen. This advance was driven mainly by novel imaging techniques, however, these have not yet been implemented in routine clinical practice. The changes in the grey matter are related to physical and cognitive disability seen in individuals with multiple sclerosis. Furthermore, damage to several grey matter structures can be associated with impairment of specific functions. Therefore, we conclude that grey matter damage - global and regional - has the potential to become a marker of disease activity, complementary to the currently used magnetic resonance markers (global brain atrophy and T2 hyperintense lesions). Furthermore, it may improve the prediction of the future disease course and response to therapy in individual patients and may also become a reliable additional surrogate marker of treatment effect
Study of the platinum nanoparticle synthesis in polyelectrolyte multilayer films and their electrical and morphological surface properties
High-Efficiency FTO-Free Counter Electrodes for Dye-Sensitized Solar Cells Based on Low-Pt-Doped Carbon Nanosheets
Highly efficient fluorine doped tin oxide (FTO)-free counter electrodes (CEs) for dye-sensitized solar cells (DSSCs) are developed by a low amount doping of Pt on carbon nanosheet (CNS)-based charge-collecting electrodes. The low Pt-doped CNS-based CEs were prepared by simple deposition of Pt by a conventional method. The CNSs had a dual function as both highly conducting charge-collecting electrodes (sheet resistance of similar to 40 Omega/sq) and decent electrocatalytic CE layers for iodine reduction. Low Pt doping (using similar to 100 times less Pt than with conventional doping) on a CNS dramatically improved the electrocatalytic activity for the I-3 reduction of the CNSs and the charge transfer resistance at CE/electrolyte interfaces, which was not possible using FTO. The performance of the low-Pt-doped CNS CEs was comparable to that of high (conventional)-Pt-doped FTO CEs. DSSCs using the low-Pt-doped CNS CEs showed a power conversion efficiency (PCE) of 7.56%, whereas those using high-Pt-doped CNS CEs showed a PCE of 8.05%. In contrast, DSSCs using low-Pt-doped FTO CEs showed a PCE of 4.50%, whereas those using high-Pt-doped FTO CEs showed a PCE of 8.21%. Pt/CNS is an intriguing CE material that can use 100 times less Pt than conventional Pt/FTO CEs, which suggests a useful strategy for reducing the fabrication cost of DSSCs
Highly efficient iodide/triiodide dye-sensitized solar cells with gel-coated reduce graphene oxide/single-walled carbon nanotube composites as the counter electrode exhibiting an open-circuit voltage of 0.90 v
10.1021/am401392kACS Applied Materials and Interfaces5146657-666
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