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1.
Expert Rev Mol Med ; 21: e7, 2019 12 04.
Artigo em Inglês | MEDLINE | ID: mdl-31796147

RESUMO

INTRODUCTION: Diabetes mellitus (DM) is the most common metabolic disease. A WHO report from 2016 indicates that 422 million people worldwide suffer from DM or hyperglycaemia because of impaired glucose metabolism. Chronic hyperglycaemia leads to micro- and macrovessel damage, which may result in life-threatening complications. The Wnt pathway regulates cell proliferation and survival by modulating the expression of genes that control cell differentiation. Three linked Wnt pathways have been discovered thus far: a ß-catenin-dependent pathway and two pathways independent of ß-catenin - the planar cell polarity pathway and calcium-dependent pathway. The Wnt pathway regulates genes associated with inflammation, cell cycle, angiogenesis, fibrinolysis and other molecular processes. AREAS COVERED: This review presents the current state of knowledge regarding the contribution of the Wnt pathway to endothelial ageing under hyperglycaemic conditions and provides new insights into the molecular basis of diabetic endothelial dysfunction. CONCLUSION: The ß-catenin-dependent pathway is a potential target in the prophylaxis and treatment of early-stage diabetes-related vascular complications. However, the underlying molecular mechanisms remain largely undetermined and require further investigation.


Assuntos
Endotélio Vascular/metabolismo , Hiperglicemia/metabolismo , Via de Sinalização Wnt , Animais , Proliferação de Células , Endotélio Vascular/patologia , Humanos , Hiperglicemia/patologia
2.
Cell Mol Biol Lett ; 23: 57, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30574165

RESUMO

BACKGROUND: Extracellular vesicles are small vesicles that contain cytoplasmic and membrane components from their paternal cells. They enter target cells through uptake to transfer their biological cargo. In this study, we investigated the process of endothelial EV internalization and created a 3D visualization of their intracellular distribution. METHODS AND RESULTS: Two immortalized endothelial cell lines that express h-TERT (human telomerase) were used for EV release: microvascular TIME and macrovascular HUVEC. EVs were isolated from the cell culture medium via differential centrifugation and used for the uptake experiments. The size distribution of the EVs was measured using TRPS technology on a qNano instrument. Internalization of EVs was observed using a Zeiss LSM 710 confocal laser microscope after staining of the EVs with PKH26. EVs were observed intracellularly and distributed in the perinuclear region of the target cells. The distribution patterns were similar in both cell lines. CONCLUSION: The perinuclear localization of the internalized EVs shows their biological stability after their uptake to the endothelial cells. The 3D visualization allows the determination of a more accurate location of EVs relative to the donor cell nucleus.


Assuntos
Vesículas Extracelulares/metabolismo , Células Endoteliais da Veia Umbilical Humana/metabolismo , Imageamento Tridimensional , Endocitose , Células Endoteliais da Veia Umbilical Humana/citologia , Humanos
3.
Pol Arch Intern Med ; 133(4)2023 04 19.
Artigo em Inglês | MEDLINE | ID: mdl-37074358

RESUMO

Extracellular vesicles (EVs) are released by all cells, both in physiological and pathological conditions. Their molecular charge and composition emerge as possible biomarkers, but EVs may also be considered for other clinical applications. This review discusses the role of other features of EVs, such as their lipid components or composition of glycans that form the EV corona and regulate EV biodistribution and uptake by target cells. The importance of EV electric charge has been discussed as a new insight into EV fate and destination.


Assuntos
Vesículas Extracelulares , Humanos , Distribuição Tecidual , Vesículas Extracelulares/metabolismo , Biomarcadores/metabolismo
4.
Comput Biol Med ; 127: 104092, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-33161334

RESUMO

With the number of affected individuals still growing world-wide, the research on COVID-19 is continuously expanding. The deep learning community concentrates their efforts on exploring if neural networks can potentially support the diagnosis using CT and radiograph images of patients' lungs. The two most popular publicly available datasets for COVID-19 classification are COVID-CT and COVID-19 Image Data Collection. In this work, we propose a new dataset which we call COVID-19 CT & Radiograph Image Data Stock. It contains both CT and radiograph samples of COVID-19 lung findings and combines them with additional data to ensure a sufficient number of diverse COVID-19-negative samples. Moreover, it is supplemented with a carefully defined split. The aim of COVID-19 CT & Radiograph Image Data Stock is to create a public pool of CT and radiograph images of lungs to increase the efficiency of distinguishing COVID-19 disease from other types of pneumonia and from healthy chest. We hope that the creation of this dataset would allow standardisation of the approach taken for training deep neural networks for COVID-19 classification and eventually for building more reliable models.


Assuntos
COVID-19/diagnóstico por imagem , Aprendizado Profundo , Pulmão/diagnóstico por imagem , Interpretação de Imagem Radiográfica Assistida por Computador/métodos , Tomografia Computadorizada por Raios X/normas , COVID-19/virologia , Humanos , SARS-CoV-2/isolamento & purificação
5.
Theranostics ; 8(14): 3874-3890, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30083267

RESUMO

Ectosomes (Ects) are a subpopulation of extracellular vesicles formed by the process of plasma membrane shedding. In the present study, we profiled ectosome-specific microRNAs (miRNAs) in patients with type 2 diabetes mellitus (T2DM) and analyzed their pro- and anti-angiogenic potential. Methods: We used different approaches for detecting and enumerating Ects, including atomic force microscopy, cryogenic transmission electron microscopy, and nanoparticle tracking analysis. Furthermore, we used bioinformatics tools to analyze functional data obtained from specific miRNA enrichment signatures during angiogenesis and vasculature development. Results: Levels of miR-193b-3p, miR-199a-3p, miR-20a-3p, miR-26b-5p, miR-30b-5p, miR-30c-5p, miR-374a-5p, miR-409-3p, and miR-95-3p were significantly different between Ects obtained from patients with T2DM and those obtained from healthy controls. Conclusion: Our results showed differences in the abundance of pro- and anti-angiogenic miRNAs in Ects of patients with T2DM, and are suggestive of mechanisms underlying the development of vascular complications due to impaired angiogenesis in such patients.


Assuntos
Moduladores da Angiogênese/análise , Micropartículas Derivadas de Células/química , Diabetes Mellitus Tipo 2/patologia , MicroRNAs/análise , MicroRNAs/genética , Neovascularização Patológica/patologia , Idoso , Idoso de 80 Anos ou mais , Biologia Computacional , Microscopia Crioeletrônica , Feminino , Humanos , Masculino , Microscopia de Força Atômica
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