P. Thi, Q. Le, V. Stoldt, N. Tran, Anh T. K. Le, Khon Huynh
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引用次数: 1
摘要
纤维连接蛋白(fibrar fi bronectin, FFN)是一种生物活性形式的纤维连接蛋白,在细胞周围形成线状和支状网络,支持细胞活动。先前的研究表明,剪切应力可以诱导无细胞FN纤维的发生。在本研究中,我们进一步考察了剪切应力条件对形成的FFN形态的影响,并初步寻找FFN形态与细胞粘附的关系。50µg/ml的血浆FN以500 s -1或4000 s -1的剪切速率通过通道载玻片灌注。我们的研究结果表明,形成了四种FFN结构:(1)FN结节,(2)不同大小的纤维brir,(3)有或没有结节附着,(4)纤维brir矩阵。在4000 s -1时,FFN在前10 min内形成,20 min后表面覆盖率达到最高。相比之下,在500 s -1时,FFN的形成明显缓慢,只形成FN结节和小纤维。血小板结合在纤薄层上,很少在大纤薄层上发现。而纤维母细胞则在FFN基质的平台上伸展其形态,并主动与各种类型的FFN结合。综上所述,我们的数据表明FFN的生物活性依赖于形态。对不同形态的FFN进行粘附试验。我们的显微分析
Morphologies of Fibronectin Fibrils Formed under Shear Conditions and Their
Cellular Adhesiveness Properties
: Fibrillar fi bronectin (FFN) is a biological active form of FN which form linear and branched meshwork around cells and support cellular activities. Previous studies have demonstrated that shear stress can induce cell-free FN fi brillogenesis. In this study, we further examined the effect of shear stress conditions on morphology of formed FFN and preliminarily looked for relationship between FFN ’ s morphology and cell adhesion. Plasma FN at 50 µg/ml was perfused through channel slides at shear rates of 500 s -1 or 4000 s -1 . Our results showed that there were four FFN structures formed: (1) FN nodules, (2) fi bril in different sizes (3) with or without nodule attachment, and (4) fi brillar matrix. At 4000 s -1 , FFN fi brils was formed within the fi rst 10 min and reached the highest surface coverage only after 20 min. In contrast, FFN formation was signi fi cant more slowly at 500 s -1 at which only FN nodules and small fi brils were formed. Platelets bound on thin layer of FN and rarely found on large FN fi brils. In contrast, fi broblast stretched their shape on platform of FFN matrix and bound actively to all types of FFNs. Taken together, our data suggests a morphological dependent biological activity of FFN. adhesion assays were performed on FFN with diverse morphologies. Our microscopic analysis
期刊介绍:
The field of biomechanics concerns with motion, deformation, and forces in biological systems. With the explosive progress in molecular biology, genomic engineering, bioimaging, and nanotechnology, there will be an ever-increasing generation of knowledge and information concerning the mechanobiology of genes, proteins, cells, tissues, and organs. Such information will bring new diagnostic tools, new therapeutic approaches, and new knowledge on ourselves and our interactions with our environment. It becomes apparent that biomechanics focusing on molecules, cells as well as tissues and organs is an important aspect of modern biomedical sciences. The aims of this journal are to facilitate the studies of the mechanics of biomolecules (including proteins, genes, cytoskeletons, etc.), cells (and their interactions with extracellular matrix), tissues and organs, the development of relevant advanced mathematical methods, and the discovery of biological secrets. As science concerns only with relative truth, we seek ideas that are state-of-the-art, which may be controversial, but stimulate and promote new ideas, new techniques, and new applications.