9 research outputs found

    A description of tides near the Chesapeake Bay entrance using in situ data with an adjoint model

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    Time series of surface elevation and current velocity in the vicinity of the Chesapeake Bay entrance are assimilated into a linear, barotropic model using an iterative adjoint method. Tide surface elevations, NOAA‐NOS tidal data, moored acoustic Doppler current profiler (ADCP), and ocean surface current radar (OSCR) data are included in the assimilation. Data are analyzed for three tidal constituents (M2, S2, O1); tidal series are constructed from these constituents and then used in the model assimilations. Statistics of predicted currents compare favorably with those calculated from data not used in the assimilation. An error analysis of the data distribution is performed for the M2 tidal component, showing lower errors near assimilation data series but large errors, particularly for velocity, at some locations. Addition of a hypothetical current mooring dramatically reduces errors over most of the domain. We believe these results give the most demonstrably accurate description now available of tidal currents for this region of strong currents and heavy shipping

    International Journal of Molecular Sciences / Loss of SR-BI Down-Regulates MITF and Suppresses Extracellular Vesicle Release in Human Melanoma

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    Melanoma is a skin tumor with a high tendency for metastasis and thus is one of the deadliest cancers worldwide. Here, we investigated the expression of the scavenger receptor class B type 1 (SR-BI), a high-density lipoprotein (HDL) receptor, and tested for its role in melanoma pigmentation as well as extracellular vesicle release. We first analyzed the expression of SR-BI in patient samples and found a strong correlation with MITF expression as well as with the melanin synthesis pathway. Hence, we asked whether SR-BI could also play a role for the secretory pathway in metastatic melanoma cells. Interestingly, gain- and loss-of-function of SR-BI revealed regulation of the proto-oncogene MET. In line, SR-BI knockdown reduced expression of the small GTPase RABB22A, the ESCRT-II protein VPS25, and SNAP25, a member of the SNARE complex. Accordingly, reduced overall extracellular vesicle generation was detected upon loss of SR-BI. In summary, SR-BI expression in human melanoma enhances the formation and transport of extracellular vesicles, thereby contributing to the metastatic phenotype. Therapeutic targeting of SR-BI would not only interfere with cholesterol uptake, but also with the secretory pathway, therefore suppressing a key hallmark of the metastatic program.(VLID)491292

    Ferrous metallurgy

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