Development of a Method for Three-Dimensional Culturing of Human Mesenchymal Stem (Stromal) Cells Using a Cellulose Matrix

被引:0
|
作者
Kuneev I.K. [1 ]
Ivanova Y.S. [1 ]
Nashchekina Y.A. [1 ]
Patronova E.K. [1 ]
Sokolova A.V. [1 ]
Domnina A.P. [1 ]
机构
[1] Institute of Cytology, Russian Academy of Sciences, St. Petersburg
基金
俄罗斯科学基金会;
关键词
3D culturing; decellularized plants; decidual differentiation; endometrial mesenchymal stem (stromal) cells;
D O I
10.1134/S1990519X2304003X
中图分类号
学科分类号
摘要
Abstract: The development of cell-culture methods in 3D systems is important and necessary for the development of significant areas of modern cell biology. When cultivating in a 3D system, the tissue-specific architecture is reproduced, with the real microenvironment and cell behavior being more accurately recreated in vivo. Human mesenchymal stem/stromal cells (MSCs) are usually isolated and cultured as a monolayer 2D culture. In this work, we have developed a method for three-dimensional culturing and tissue-specific decidual differentiation of MSCs isolated from human endometrial tissue using a matrix obtained from a decellularized apple. Decellularized apple matrices have sufficient mechanical strength; are biocompatible, affordable, and easy to use; and have ample possibilities for surface modification. This system of cell culturing is suitable for studies using both confocal microscopy and flow cytometry. The model we have developed can become the basis for creating new cell products and tissue engineering structures for the needs of regenerative biomedicine. © 2023, Pleiades Publishing, Ltd.
引用
收藏
页码:388 / 397
页数:9
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