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聚多巴胺介导的蛋白质吸附改变原代人脂肪来源干细胞(hASCs)的表观遗传状态和分化。

Polydopamine-Mediated Protein Adsorption Alters the Epigenetic Status and Differentiation of Primary Human Adipose-Derived Stem Cells (hASCs).

作者信息

Harati Javad, Tao Xuelian, Shahsavarani Hosein, Du Ping, Galluzzi Massimiliano, Liu Kun, Zhang Zhen, Shaw Peter, Shokrgozar Mohammad Ali, Pan Haobo, Wang Peng-Yuan

机构信息

Shenzhen Key Laboratory of Biomimetic Materials and Cellular Immunomodulation, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China.

Shenzhen College of Advanced Technology, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Front Bioeng Biotechnol. 2022 Aug 10;10:934179. doi: 10.3389/fbioe.2022.934179. eCollection 2022.

Abstract

Polydopamine (PDA) is a biocompatible cell-adhesive polymer with versatile applications in biomedical devices. Previous studies have shown that PDA coating could improve cell adhesion and differentiation of human mesenchymal stem cells (hMSCs). However, there is still a knowledge gap in the effect of PDA-mediated protein adsorption on the epigenetic status of MSCs. This work used gelatin-coated cell culture surfaces with and without PDA underlayer (Gel and PDA-Gel) to culture and differentiate primary human adipose-derived stem cells (hASCs). The properties of these two substrates were significantly different, which, in combination with a variation in extracellular matrix (ECM) protein bioactivity, regulated cell adhesion and migration. hASCs reduced focal adhesions by downregulating the expression of integrins such as αV, α1, α2, and β1 on the PDA-Gel compared to the Gel substrate. Interestingly, the ratio of H3K27me3 to H3K27me3+H3K4me3 was decreased, but this only occurred for upregulation of and genes during chondrogenic differentiation. This result implies that the PDA-Gel surface positively affects the chondrogenic, but not adipogenic and osteogenic, differentiation. In conclusion, for the first time, this study demonstrates the sequential effects of PDA coating on the biophysical property of adsorbed protein and then focal adhesions and differentiation of hMSCs through epigenetic regulation. This study sheds light on PDA-mediated mechanotransduction.

摘要

聚多巴胺(PDA)是一种具有生物相容性的细胞粘附聚合物,在生物医学设备中有广泛应用。先前的研究表明,PDA涂层可以改善人间充质干细胞(hMSCs)的细胞粘附和分化。然而,关于PDA介导的蛋白质吸附对间充质干细胞表观遗传状态的影响,仍存在知识空白。这项工作使用了有无PDA底层的明胶包被的细胞培养表面(Gel和PDA-Gel)来培养和分化原代人脂肪来源干细胞(hASCs)。这两种底物的性质有显著差异,与细胞外基质(ECM)蛋白生物活性的变化相结合,调节细胞粘附和迁移。与Gel底物相比,hASCs在PDA-Gel上通过下调整合素如αV、α1、α2和β1的表达来减少粘着斑。有趣的是,H3K27me3与H3K27me3+H3K4me3的比值降低,但这仅发生在软骨形成分化过程中 和 基因上调时。这一结果表明,PDA-Gel表面对软骨形成分化有积极影响,但对脂肪形成和成骨分化没有影响。总之,本研究首次证明了PDA涂层对吸附蛋白的生物物理性质、进而对hMSCs的粘着斑和通过表观遗传调控的分化的顺序效应。这项研究揭示了PDA介导的机械转导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daa1/9399727/a81eb3c59c87/fbioe-10-934179-g001.jpg

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