RESUMEN
Neutrophils are innate immune cells that are key to protecting the host against infection and maintaining body homeostasis. However, if dysregulated, they can contribute to disease, such as in cancer or chronic autoinflammatory disorders. Recent studies have highlighted the heterogeneity in the neutrophil compartment and identified the presence of immature neutrophils and their precursors in these pathologies. Therefore, understanding neutrophil maturity and the mechanisms through which they contribute to disease is critical. Neutrophils were first characterized morphologically by Ehrlich in 1879 using microscopy, and since then, different technologies have been used to assess neutrophil maturity. The advances in the imaging field, including state-of-the-art microscopy and machine learning algorithms for image analysis, reinforce the use of neutrophil nuclear morphology as a fundamental marker of maturity, applicable for objective classification in clinical diagnostics. New emerging approaches, such as the capture of changes in chromatin topology, will provide mechanistic links between the nuclear shape, chromatin organization, and transcriptional regulation during neutrophil maturation.
Asunto(s)
Cromatina , Neutrófilos , Regulación de la Expresión GénicaRESUMEN
PURPOSE: Thoracic aortic dissection (TAD) is considered one of the most catastrophic and non-traumatic cardiovascular diseases associated with high morbidity and mortality rates in clinical treatment. The purpose of this paper is to investigate the pulsatile hemodynamics changes throughout a cardiac cycle in a Stanford Type B TAD model with the aid of computational fluid dynamics (CFD) method. METHODS: A patient-specific dissected aorta geometry was reconstructed from the three-dimensional (3D) computed tomography angiography (CTA) scanning. The realistic time-dependent pulsatile boundary conditions were prescribed for our 3D patient-specific TAD model. Blood was considered to be an incompressible, Newtonian fluid. The aortic wall was assumed to be rigid, and a no-slip boundary condition was applied at the wall. CFD simulations were processed using the finite volume (FV) method to investigate the pulsatile hemodynamics in terms of blood flow velocity, aortic wall pressure, wall shear stress and flow vorticity. In the experiments, blood velocity, pressure, wall shear stress and vorticity distributions were analyzed qualitatively and quantitatively. RESULTS: The experimental results demonstrated a high wall shear stress and strong vertical flow at dissection initiation. The results also indicated that wall shear progressed along the false lumen, which is a possible cause of blood flow between aortic wall layers.