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仿生同心微槽钛表面通过 H3K4 三甲基化表观遗传调控影响骨髓间充质干细胞成骨分化。

Biomimetic concentric microgrooved titanium surfaces influence bone marrow-derived mesenchymal stem cell osteogenic differentiation via H3K4 trimethylation epigenetic regulation.

机构信息

Department of Stomatology, Engineering Research Center of Fujian University for Stomatological Biomaterials, Xiamen Medical College.

Stomatological Hospital of Xiamen Medical college.

出版信息

Dent Mater J. 2024 Sep 28;43(5):683-692. doi: 10.4012/dmj.2023-327. Epub 2024 Aug 10.

Abstract

Material surface micromorphology can modulate cellular behavior and promote osteogenic differentiation through cytoskeletal rearrangement. Bone reconstruction requires precise regulation of gene expression in cells, a process governed by epigenetic mechanisms such as histone modifications, DNA methylation, and chromatin remodeling. We constructed osteon-mimetic concentric microgrooved titanium surfaces with different groove sizes and cultured bone marrow-derived mesenchymal stem cells (BMSCs) on the material surfaces to study how they regulate cell biological behavior and osteogenic differentiation through epigenetics. We found that the cells arranged in concentric circles along the concentric structure in the experimental group, and the concentric microgrooved surface did not inhibit cell proliferation. The results of a series of osteogenic differentiation experiments showed that the concentric microgrooves facilitated calcium deposition and promoted osteogenic differentiation of the BMSCs. Concentric microgrooved titanium surfaces that were 30 μm wide and 10 μm deep promoted osteogenic differentiation of BMSC by increasing WDR5 expression via H3K4 trimethylation upregulation.

摘要

材料表面的微观形貌可以通过细胞骨架重排来调节细胞行为并促进成骨分化。骨重建需要精确调节细胞中的基因表达,这个过程受到表观遗传机制的调控,如组蛋白修饰、DNA 甲基化和染色质重塑。我们构建了具有不同槽宽的仿生骨单元同心微槽钛表面,并在材料表面培养骨髓间充质干细胞(BMSCs),以研究它们如何通过表观遗传学调节细胞生物学行为和成骨分化。我们发现细胞沿着实验组的同心结构呈同心排列,而同心微槽表面并不抑制细胞增殖。一系列成骨分化实验的结果表明,同心微槽促进了钙沉积并促进了 BMSCs 的成骨分化。30μm 宽、10μm 深的同心微槽钛表面通过上调 H3K4 三甲基化来增加 WDR5 表达,从而促进 BMSC 的成骨分化。

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