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细胞铺展面积对间充质干细胞成骨定向分化及表型维持的影响。

Influence of Cell Spreading Area on the Osteogenic Commitment and Phenotype Maintenance of Mesenchymal Stem Cells.

机构信息

Research Center for Functional Materials, National Institute for Materials Science, 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.

Department of Materials Science and Engineering, Graduate School of Pure and Applied Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8577, Japan.

出版信息

Sci Rep. 2019 May 3;9(1):6891. doi: 10.1038/s41598-019-43362-9.

Abstract

Osteogenic differentiation and commitment of mesenchymal stem cells (MSCs) is a complex process that is induced and regulated by various biological factors and biophysical cues. Although cell spreading area, as a biophysical cue, has been demonstrated to play a critical role in the regulation of osteogenic differentiation of MSCs, it is unclear how it affects the maintenance of the committed phenotype after osteogenic differentiation of MSCs. In this study, poly (vinyl alcohol) was micropatterned on a tissue culture polystyrene surface, and the micropatterns were used to culture MSCs to control their cell spreading area. The influence of cell spreading area on osteogenic differentiation and maintenance of the differentiated phenotype of MSCs was investigated. MSCs with a larger spreading area showed a higher degree of osteogenic differentiation, slower loss of differentiated phenotype and slower re-expression of stem cell markers compared with MSCs with a smaller spreading area. A large cell spreading area was beneficial for osteogenic differentiation of MSCs and maintenance of their differentiated phenotype.

摘要

成骨细胞分化和间充质干细胞(MSCs)的定向是一个复杂的过程,受到各种生物因子和生物物理线索的诱导和调节。尽管细胞铺展面积作为一种生物物理线索,已被证明在调节 MSC 的成骨分化中起着关键作用,但尚不清楚它如何影响 MSC 成骨分化后定向表型的维持。在这项研究中,将聚乙烯醇(PVA)微图案化到组织培养聚苯乙烯表面上,并用微图案来培养 MSC 以控制其细胞铺展面积。研究了细胞铺展面积对 MSC 成骨分化和分化表型维持的影响。与铺展面积较小的 MSC 相比,铺展面积较大的 MSC 表现出更高程度的成骨分化,较慢的分化表型丧失和较慢的干细胞标志物再表达。较大的细胞铺展面积有利于 MSC 的成骨分化和分化表型的维持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4fc5/6499796/4bf3c2cb340d/41598_2019_43362_Fig1_HTML.jpg

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