Julia Rieber, Roger Khalid Niederhauser, Pietro Giovanoli, Johanna Buschmann
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引用次数: 0
摘要
第一个数据集是指基质金属蛋白酶-1 (TIMP-1)蛋白的组织抑制剂包含到DegraPol®纤维中,利用乳液静电纺丝和随机纤维网的表征。具体来说,在7天内研究了蛋白质从网状物中的释放动力学。此外,还确定了静、动态水接触角。最后,我们评估了含TIMP-1和不含TIMP-1的DegraPol®的傅里叶变换红外光谱(FTIR)。第二个数据集是用Alamar Blue Assay获得的增殖数据,应用于兔跟腱细胞和兔脂肪来源的干细胞,当在体外添加1、10和100 ng/mL TIMP-1刺激时,与不添加TIMP-1的相应细胞培养(对照)相比。此外,我们进行了qPCR,并在分别添加1、10和100 ng/mL TIMP-1体外刺激的两种细胞类型中分别获得了胶原I、ki67、tenomodulin和碱性磷酸酶基因表达数据,并且与不添加TIMP-1的细胞培养基(对照)相比,数据以多种诱导形式呈现。
Release kinetics, static and dynamic water contact angles and FTIR data for tissue inhibitor of matrix metalloprotease-1 (TIMP-1) incorporated in electrospun random DegraPol® fibers and TIMP-1 impact on tenocytes and adipose-derived stem cells proliferation and gene expression data
A first data set refers to tissue inhibitor of matrix metalloprotease-1 (TIMP-1) protein inclusion into a DegraPol® fibres utilizing emulsion electrospinning and the characterization of the random fibre mesh. Specifically, the release kinetics of the protein from the mesh was studied over 7 days. Moreover, the static and the dynamic water contact angles were determined. Finally, we assessed Fourier-Transformed Infrared Spectra (FTIR spectra) for DegraPol® with and without TIMP-1.
A second data set represents proliferation data obtained with the Alamar Blue Assay, applied on rabbit Achilles tenocytes and rabbit adipose-derived stem cells, when stimulated in vitro with 1, 10, and 100 ng/mL TIMP-1 supplementation compared to the corresponding cell culture without TIMP-1 (control). Furthermore, qPCR was performed and collagen I, ki67, tenomodulin and alkaline phosphatase gene expression data are presented for both cell types in vitro stimulated with 1, 10, and 100 ng/mL TIMP-1 supplementation, respectively, and data are presented as manifold induction compared to a TIMP-1-free cell culture medium (control).
期刊介绍:
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