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人骨髓间充质干细胞在细胞外基质和钛片上的黏附:比较激酶组谱分析。

Human mesenchymal stromal cells in adhesion to cell-derived extracellular matrix and titanium: Comparative kinome profile analysis.

机构信息

Department of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Department of Gastroenterology and Hepatology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

J Cell Physiol. 2019 Mar;234(3):2984-2996. doi: 10.1002/jcp.27116. Epub 2018 Jul 30.

Abstract

The extracellular matrix (ECM) physically supports cells and influences stem cell behaviour, modulating kinase-mediated signalling cascades. Cell-derived ECMs have emerged in bone regeneration as they reproduce physiological tissue-architecture and ameliorate mesenchymal stromal cell (MSC) properties. Titanium scaffolds show good mechanical properties, facilitate cell adhesion, and have been routinely used for bone tissue engineering (BTE). We analyzed the kinomic signature of human MSCs in adhesion to an osteopromotive osteoblast-derived ECM, and compared it to MSCs on titanium. PamChip kinase-array analysis revealed 63 phosphorylated peptides on ECM and 59 on titanium, with MSCs on ECM exhibiting significantly higher kinase activity than on titanium. MSCs on the two substrates showed overlapping kinome profiles, with activation of similar signalling pathways (FAK, ERK, and PI3K signalling). Inhibition of PI3K signalling in cells significantly reduced adhesion to ECM and increased the number of nonadherent cells on both substrates. In summary, this study comprehensively characterized the kinase activity in MSCs on cell-derived ECM and titanium, highlighting the role of PI3K signalling in kinomic changes regulating osteoblast viability and adhesion. Kinome profile analysis represents a powerful tool to select pathways to better understand cell behaviour. Osteoblast-derived ECM could be further investigated as titanium scaffold-coating to improve BTE.

摘要

细胞外基质 (ECM) 物理支撑细胞并影响干细胞行为,调节激酶介导的信号级联。细胞衍生的 ECM 在骨再生中出现,因为它们再现了生理组织架构并改善了间充质基质细胞 (MSC) 的特性。钛支架具有良好的机械性能,促进细胞黏附,已常规用于骨组织工程 (BTE)。我们分析了人 MSC 在黏附于促骨生成的成骨细胞衍生 ECM 时的激酶组学特征,并将其与在钛上的 MSC 进行了比较。PamChip 激酶阵列分析显示 ECM 上有 63 个磷酸化肽,钛上有 59 个,ECM 上的 MSC 激酶活性明显高于钛上的 MSC。两种基质上的 MSC 表现出重叠的激酶组谱,激活了类似的信号通路 (FAK、ERK 和 PI3K 信号)。在细胞中抑制 PI3K 信号显著降低了对 ECM 的黏附,并增加了两种基质上的非黏附细胞数量。总之,这项研究全面描述了 MSC 在细胞衍生的 ECM 和钛上的激酶活性,强调了 PI3K 信号在调节成骨细胞活力和黏附的激酶组变化中的作用。激酶组谱分析代表了一种选择途径以更好地理解细胞行为的强大工具。成骨细胞衍生的 ECM 可以进一步作为钛支架涂层进行研究,以改善 BTE。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25c2/6585805/309f1819c149/JCP-234-2984-g001.jpg

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