Human umbilical cord blood mesenchymal stem cells expansion via human fibroblast-derived matrix and their potentials toward regenerative application

被引:11
|
作者
Van, Se Young [1 ]
Noh, Yong Kwan [1 ,2 ]
Kim, Seong Who [3 ]
Oh, Yeon Mok [4 ]
Kim, Ik Hwan [2 ]
Park, Kwideok [1 ,5 ]
机构
[1] Korea Inst Sci & Technol, Ctr Biomat, Seoul 02792, South Korea
[2] Korea Univ, Dept Biotechnol, Seoul 02841, South Korea
[3] Univ Ulsan, Asan Med Ctr, Coll Med, Dept Biochem & Mol Biol, Seoul 05505, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Pulm & Crit Care Med, Seoul 05505, South Korea
[5] Korea Univ Sci & Technol UST, KIST Sch, Div Biomed Sci & Technol, Seoul 02792, South Korea
关键词
Extracellular matrix (ECM); Human fibroblast-derived matrix (hFDM); Umbilical cord blood-derived mesenchymal stem cells (UCB-MSCs); MSCs expansion; Emphysema; MULTI-LINEAGE DIFFERENTIATION; BONE-MARROW; EXTRACELLULAR-MATRIX; EX-VIVO;
D O I
10.1007/s00441-018-2971-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Large expansion of human mesenchymal stem cells (MSCs) is of great interest for clinical applications. In this study, we examine the feasibility of human fibroblast-derived extracellular matrix (hFDM) as an alternative cell expansion setting. hFDM is obtained from decellularized extracellular matrix (ECM) derived from in vitro cultured human lung fibroblasts. Our study directly compares conventional platforms (tissue culture plastic (TCP), fibronectin (FN)-coated TCP) with hFDM using umbilical cord blood-derived MSCs (UCB-MSCs). Early cell morphology shows a rather rounded shape on TCP but highly elongated morphology on hFDM. Cell proliferation demonstrates that MSCs on hFDM were significantly better compared to the others in both 10 and 2% serum condition. Cell migration assay suggests that cell motility was improved and a cell migration marker CXCR4 was notably up-regulated on hFDM. MSCs differentiation into osteogenic lineage on hFDM was also very effective as examined via gene expression, von Kossa staining and alkaline phosphatase activity. In addition, as the MSCs were expanded on each substrate, transferred to 3D polymer mesh scaffolds and then cultivated for a while, the data found better cell proliferation and more CXCR4 expression with MSCs pre-conditioned on hFDM. Moreover, higher gene expression of stemness and engraftment-related markers was noticed with the hFDM group. Furthermore when UCB-MSCs expanded on TCP or hFDM were injected into emphysema (a lung disease) animal model, the results indicate that MSCs pre-conditioned on hFDM (with 2% serum) retain more advanced therapeutic efficacy on the improvement of emphysema than those on TCP. Current works demonstrate that compared to the conventional platforms, hFDM can be a promising source of cell expansion with a naturally derived biomimetic ECM microenvironment and may find some practical applications in regenerative medicine.
引用
收藏
页码:233 / 245
页数:13
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