首页> 美国卫生研究院文献>Springer Open Choice >Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy
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Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy

机译:分子的拓扑结构和膜纳米结构。脾切除术后遗传性红细胞增多症中的红细胞通过原子力显微镜检查患者

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摘要

Hereditary spherocytosis is an inherited red blood cell membrane disorder resulting from mutations of genes encoding erythrocyte membrane and cytoskeletal proteins. Few equipments can observe the structural characteristics of hereditary spherocytosis directly expect for atomic force microscopy In our study, we proved atomic force microscopy is a powerful and sensitive instrument to describe the characteristics of hereditary spherocytosis. Erythrocytes from hereditary spherocytosis patients were small spheroidal, lacking a well-organized lattice on the cell membrane, with smaller cell surface particles and had reduced valley to peak distance and average cell membrane roughness vs. those from healthy individuals. These observations indicated defects in the certain cell membrane structural proteins such as α- and β-spectrin, ankyrin, etc. Until now, splenectomy is still the most effective treatment for symptoms relief for hereditary spherocytosis. In this study, we further solved the mysteries of membrane nanostructure changes of erythrocytes before and after splenectomy in hereditary spherocytosis by atomic force microscopy. After splenectomy, the cells were larger, but still spheroidal-shaped. The membrane ultrastructure was disorganized and characterized by a reduced surface particle size and lower than normal Ra values. These observations indicated that although splenectomy can effectively relieve the symptoms of hereditary spherocytosis, it has little effect on correction of cytoskeletal membrane defects of hereditary spherocytosis. We concluded that atomic force microscopy is a powerful tool to investigate the pathophysiological mechanisms of hereditary spherocytosis and to monitor treatment efficacy in clinical practices. To the best of our knowledge, this is the first report to study hereditary spherocytosis with atomic force microscopy and offers important mechanistic insight into the underlying role of splenectomy.
机译:遗传性球囊病是一种遗传性红细胞膜疾病,是由编码红细胞膜和细胞骨架蛋白的基因突变引起的。很少有设备可以直接观察到原子力显微镜所期望的遗传性球囊细胞增多症的结构特征。在我们的研究中,我们证明了原子力显微镜法是描述遗传性球囊细胞增多症特征的强大而灵敏的仪器。与健康个体相比,遗传性球囊增多症患者的红细胞为小球形,细胞膜上缺乏组织良好的晶格,细胞表面颗粒更小,谷峰距离和平均细胞膜粗糙度降低。这些观察结果表明某些细胞膜结构蛋白如α-和β-血影蛋白,锚蛋白等存在缺陷。到目前为止,脾切除术仍然是减轻遗传性球菌病症状的最有效方法。在这项研究中,我们通过原子力显微镜进一步解决了遗传性球囊炎脾切除前后红细胞膜纳米结构变化的奥秘。脾切除后,细胞较大,但仍为球形。膜超微结构杂乱无章,其特征是表面粒径减小且Ra值低于正常值。这些观察结果表明,尽管脾切除术可以有效地缓解遗传性球菌病的症状,但对校正遗传性球菌病的细胞骨架膜缺陷几乎没有影响。我们得出的结论是,原子力显微镜是研究遗传性球囊细胞增多症的病理生理机制并监测临床实践中疗效的有力工具。据我们所知,这是第一份使用原子力显微镜研究遗传性球囊细胞增多症的报告,并为了解脾切除术的潜在作用提供了重要的力学见解。

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