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1.
EMBO J ; 38(15): e95874, 2019 08 01.
Artigo em Inglês | MEDLINE | ID: mdl-31267558

RESUMO

MAPK inhibitors (MAPKi) show outstanding clinical response rates in melanoma patients harbouring BRAF mutations, but resistance is common. The ability of melanoma cells to switch from melanocytic to mesenchymal phenotypes appears to be associated with therapeutic resistance. High-throughput, subcellular proteome analyses and RNAseq on two panels of primary melanoma cells that were either sensitive or resistant to MAPKi revealed that only 15 proteins were sufficient to distinguish between these phenotypes. The two proteins with the highest discriminatory power were PTRF and IGFBP7, which were both highly upregulated in the mesenchymal-resistant cells. Proteomic analysis of CRISPR/Cas-derived PTRF knockouts revealed targets involved in lysosomal activation, endocytosis, pH regulation, EMT, TGFß signalling and cell migration and adhesion, as well as a significantly reduced invasive index and ability to form spheres in 3D culture. Overexpression of PTRF led to MAPKi resistance, increased cell adhesion and sphere formation. In addition, immunohistochemistry of patient samples showed that PTRF expression levels were a significant biomarker of poor progression-free survival, and IGFBP7 levels in patient sera were shown to be higher after relapse.


Assuntos
Resistencia a Medicamentos Antineoplásicos , Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina/metabolismo , Melanoma/metabolismo , Inibidores de Proteínas Quinases/farmacologia , Proteômica/métodos , Proteínas de Ligação a RNA/metabolismo , Adulto , Idoso , Carbamatos/farmacologia , Adesão Celular , Linhagem Celular Tumoral , Progressão da Doença , Transição Epitelial-Mesenquimal , Feminino , Regulação Neoplásica da Expressão Gênica/efeitos dos fármacos , Humanos , Proteínas de Ligação a Fator de Crescimento Semelhante a Insulina/sangue , Masculino , Melanoma/tratamento farmacológico , Melanoma/genética , Pessoa de Meia-Idade , Mapas de Interação de Proteínas , Análise de Sequência de RNA , Sulfonamidas/farmacologia , Análise de Sobrevida , Regulação para Cima , Vemurafenib/farmacologia
2.
Nano Lett ; 17(12): 8018-8023, 2017 12 13.
Artigo em Inglês | MEDLINE | ID: mdl-29199833

RESUMO

Imaging techniques can be compromised by aberrations. Especially when imaging through biological specimens, sample-induced distortions can limit localization accuracy. In particular, this phenomenon affects localization microscopy, traction force measurements, and single-particle tracking, which offer high-resolution insights into biological tissue. Here we present a method for quantifying and correcting the optical distortions induced by single, adherent, living cells. The technique uses periodically patterned gold nanostructures as a reference framework to quantify optically induced displacements with micrometer-scale sampling density and an accuracy of a few nanometers. The 3D cell shape and a simplified geometrical optics approach are then utilized to remap the microscope image. Our experiments reveal displacements of up to several hundred nanometers, and in corrected images these distortions are reduced by a factor of 3. Conversely, the relationship between cell shape and distortion provides a novel method of 3D cell shape reconstruction from a single image, enabling label-free 3D cell analysis.

3.
Sci Rep ; 6: 19135, 2016 Jan 28.
Artigo em Inglês | MEDLINE | ID: mdl-26817435

RESUMO

In industrial settings, X-ray computed tomography scans are a common tool for inspection of objects. Often the object can not be imaged using standard circular or helical trajectories because of constraints in space or time. Compared to medical applications the variance in size and materials is much larger. Adapting the acquisition trajectory to the object is beneficial and sometimes inevitable. There are currently no sophisticated methods for this adoption. Typically the operator places the object according to his best knowledge. We propose a detectability index based optimization algorithm which determines the scan trajectory on the basis of a CAD-model of the object. The detectability index is computed solely from simulated projections for multiple user defined features. By adapting the features the algorithm is adapted to different imaging tasks. Performance of simulated and measured data was qualitatively and quantitatively assessed.The results illustrate that our algorithm not only allows more accurate detection of features, but also delivers images with high overall quality in comparison to standard trajectory reconstructions. This work enables to reduce the number of projections and in consequence scan time by introducing an optimization algorithm to compose an object specific trajectory.

4.
Sci Rep ; 3: 2606, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24008441

RESUMO

The behaviour of an organism often reflects a strategy for coping with its environment. Such behaviour in higher organisms can often be reduced to a few stereotyped modes of movement due to physiological limitations, but finding such modes in amoeboid cells is more difficult as they lack these constraints. Here, we examine cell shape and movement in starved Dictyostelium amoebae during migration toward a chemoattractant in a microfluidic chamber. We show that the incredible variety in amoeboid shape across a population can be reduced to a few modes of variation. Interestingly, cells use distinct modes depending on the applied chemical gradient, with specific cell shapes associated with shallow, difficult-to-sense gradients. Modelling and drug treatment reveals that these behaviours are intrinsically linked with accurate sensing at the physical limit. Since similar behaviours are observed in a diverse range of cell types, we propose that cell shape and behaviour are conserved traits.


Assuntos
Forma Celular/fisiologia , Quimiotaxia/fisiologia , Dictyostelium/citologia , Dictyostelium/fisiologia , Modelos Biológicos
5.
Environ Sci Technol ; 41(1): 112-8, 2007 Jan 01.
Artigo em Inglês | MEDLINE | ID: mdl-17265935

RESUMO

The effect of dissolved Zn, Co, Pb, Mg, and Ca on the uptake of cadmium by biogenic aragonite was investigated. Experiments were performed in batch-reactors using metal-cadmium-bearing solutions and shell fragments with diameters in different ranges, the solid/liquid ratio being 10 grams per liter. Different initial concentrations of cadmium and metals (1.0-0.005 mM) were used. Uptake takes place via heterogeneous nucleation of metal-bearing crystallites onto the shell surfaces. Cadmium removal occurs by surface precipitation of otavite. Under the conditions used here, Co and Ca as well as Pb < or = 0.3 mM and Zn < or = 0.3 mM do not have a significant effect on the removal of cadmium. At higher concentrations, Pb and Zn outcompete Cd for the dissolving carbonate ions and thus decrease significantly the Cd removal rates. In contrast, Mg has a slight enhancing effect. Pb and Zn are removed faster than Cd, precipitating as PbCO3, Pb3(CO3)2(OH)2, and Zn5(CO3)2(OH)6. Within 24-72 h, the concentrations of lead, cadmium, and zinc decrease until approximately 0.5 microM, and the presence of aragonite buffers the solution to a pH above 8 avoiding redissolution. The study demonstrates the high effectiveness of biogenic aragonite in removing Cd and other metals from polluted waters.


Assuntos
Cádmio/química , Carbonato de Cálcio/química , Eliminação de Resíduos Líquidos/métodos , Poluentes Químicos da Água/isolamento & purificação , Purificação da Água/métodos , Cádmio/isolamento & purificação , Cátions/química , Microscopia Eletrônica de Varredura , Tamanho da Partícula , Análise Espectral Raman
6.
J Am Chem Soc ; 126(28): 8660-1, 2004 Jul 21.
Artigo em Inglês | MEDLINE | ID: mdl-15250712

RESUMO

This paper reports a simple way to synthesize an allenylidene rhenium(VII) complex. The diimido adamantyl-thiolato allenylidene rhenium(VII) complex 2 was obtained through a metathetical reaction of phosphonioalkylidyne rhenium complex 1 with diphenylketene and also structurally analyzed with X-ray diffraction. Complex 2 is the first d0 allenylidene complex with structure information.

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