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Quantifying the relation between adhesion ligand-receptor bond formation and cell phenotype

机译:量化粘附配体-受体键形成与细胞表型之间的关系

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One of the fundamental interactions in cell biology is the binding of cell receptors to adhesion ligands, and many aspects of cell behavior are believed to be regulated by the number of these bonds that form. Unfortunately, a lack of methods to quantify bond formation, especially for cells in 3D cultures or tissues, has precluded direct probing of this assumption. We now demonstrate that a FRET technique can be used to quantify the number of bonds formed between cellular receptors and synthetic adhesion oligopeptides coupled to an artificial extracellular matrix. Similar quantitative relations were found between bond number and the proliferation and differentiation of MC3T3-E1 preosteoblasts and C2C12 myoblasts, although the relation was distinct for each cell type. This approach to understanding 3D cell-extracellular matrix interactions will allow one to both predict cell behavior and to use bond number as a fundamental design criteria for synthetic extracellular matrices.
机译:细胞生物学中的基本相互作用之一是细胞受体与粘附配体的结合,并且细胞行为的许多方面被认为受形成的这些键的数目的调节。不幸的是,尤其是对于3D培养物或组织中的细胞,缺乏量化键形成的方法的方法无法直接探究此假设。现在,我们证明了FRET技术可用于量化细胞受体和耦合到人工细胞外基质的合成粘附寡肽之间形成的键数。在键数与MC3T3-E1前成骨细胞和C2C12成肌细胞的增殖和分化之间发现了相似的数量关系,尽管每种细胞类型的关系不同。这种了解3D细胞与细胞外基质相互作用的方法将使人们既可以预测细胞行为,又可以使用键数作为合成细胞外基质的基本设计标准。

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