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三维培养通过放松细胞骨架张力增加间充质干细胞中多能基因的表达。

3D culture increases pluripotent gene expression in mesenchymal stem cells through relaxation of cytoskeleton tension.

作者信息

Zhou Ying, Chen Haiyan, Li Hong, Wu Yaojiong

机构信息

School of Life Sciences, Tsinghua University, Beijing, China.

The Shenzhen Key Laboratory of Health Sciences and Technology, Graduate School at Shenzhen, Tsinghua University, Shenzhen, China.

出版信息

J Cell Mol Med. 2017 Jun;21(6):1073-1084. doi: 10.1111/jcmm.12946. Epub 2017 Mar 9.

Abstract

Three-dimensional (3D) culture has been shown to improve pluripotent gene expression in mesenchymal stem cells (MSCs), but the underlining mechanisms were poorly understood. Here, we found that the relaxation of cytoskeleton tension of MSCs in 3D culture was critically associated with the expressional up-regulation of Nanog. Cultured in spheroids, MSCs showed decreased integrin-based cell-matrix adhesion but increased cadherin-based cell-cell interaction. Different from that in 2D culture, where MSCs exhibited branched and multiple-directed F-actin stress bundles at the cell edge and strengthened stress fibres transversing the cell body, MSCs cultured in spheroids showed compact cell body, relaxed cytoskeleton tension with very thin cortical actin filament outlining the cell, and increased expression of Nanog along with reduced levels of Suv39h1 (H3K9 methyltransferase) and H3K9me3. Notably, pharmaceutical inhibition of actin polymerization with cytochalasin D or silencing Suv39h1 expression with siRNA in 2D-cultured MSCs elevated the expression of Nanog via H3K9 demethylation. Thus, our data suggest that 3D culture increases the expression of Nanog through the relaxation of actin cytoskeleton, which mediates reduced Suv39h1 and H3K9me3 levels.

摘要

三维(3D)培养已被证明可改善间充质干细胞(MSCs)中多能基因的表达,但其潜在机制尚不清楚。在这里,我们发现3D培养中MSCs细胞骨架张力的松弛与Nanog的表达上调密切相关。在球体中培养时,MSCs显示基于整合素的细胞-基质粘附减少,但基于钙粘蛋白的细胞-细胞相互作用增加。与二维培养不同,二维培养中MSCs在细胞边缘表现出分支且多向的F-肌动蛋白应力束,并加强了横穿细胞体的应力纤维,而在球体中培养的MSCs显示出紧密的细胞体,细胞骨架张力松弛,细胞周围有非常细的皮质肌动蛋白丝勾勒出细胞轮廓,并且Nanog表达增加,同时Suv39h1(H3K9甲基转移酶)和H3K9me3水平降低。值得注意的是,用细胞松弛素D对二维培养的MSCs进行肌动蛋白聚合的药物抑制或用siRNA沉默Suv39h1表达可通过H3K9去甲基化提高Nanog的表达。因此,我们的数据表明,3D培养通过肌动蛋白细胞骨架的松弛增加Nanog的表达,这介导了Suv39h1和H3K9me3水平的降低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a5e5/5431137/42e42951dbfd/JCMM-21-1073-g001.jpg

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