Wharton's jelly-derived mesenchymal cells as a new source for the generation of microtissues for tissue engineering applications

被引:13
作者
Durand-Herrera, D. [1 ,2 ,3 ]
Campos, F. [1 ,3 ]
Jaimes-Parra, B. D. [1 ]
Sanchez-Lopez, J. D. [4 ]
Fernandez-Valades, R. [3 ,5 ]
Alaminos, M. [1 ,3 ]
Campos, A. [1 ,3 ]
Carriel, V. [1 ,3 ]
机构
[1] Univ Granada, Tissue Engn Grp, Dept Histol, Granada, Spain
[2] Univ Granada, Doctoral Programme Biomed, Granada, Spain
[3] Inst Invest Biosanitaria Ibs GRANADA, Granada, Spain
[4] Univ Hosp Complex Granada, Div Maxillofacial Surg, Granada, Spain
[5] Univ Hosp Complex Granada, Div Pediat Surg, Granada, Spain
关键词
Tissue engineering; Human Wharton-jelly mesenchymal cells; Human fibroblast; Microtissues; Microaggregates; Mesenchymal stem cells; Natural biomaterial; STEM-CELLS; BIOMATERIALS; SUBSTITUTE; EXPRESSION; VIABILITY; CULTURE;
D O I
10.1007/s00418-018-1685-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microtissues (MT) are currently considered as a promising alternative for the fabrication of natural, 3D biomimetic functional units for the construction of bio-artificial substitutes by tissue engineering (TE). The aim of this study was to evaluate the possibility of generating mesenchymal cell-based MT using human umbilical cord Wharton's jelly stromal cells (WJSC-MT). MT were generated using agarose microchips and evaluated ex vivo during 28days. Fibroblasts MT (FIB-MT) were used as control. Morphometry, cell viability and metabolism, MT-formation process and ECM synthesis were assessed by phase-contrast microscopy, functional biochemical assays, and histological analyses. Morphometry revealed a time-course compaction process in both MT, but WJSC-MT resulted to be larger than FIB-MT in all days analyzed. Cell viability and functionality evaluation demonstrated that both MT were composed by viable and metabolically active cells, especially the WJSC during 4-21days ex vivo. Histology showed that WJSC acquired a peripheral pattern and synthesized an extracellular matrix-rich core over the time, what differed from the homogeneous pattern observed in FIB-MT. This study demonstrates the possibility of using WJSC to create MT containing viable and functional cells and abundant extracellular matrix. We hypothesize that WJSC-MT could be a promising alternative in TE protocols. However, future cell differentiation and in vivo studies are still needed to demonstrate the potential usefulness of WJSC-MT in regenerative medicine.
引用
收藏
页码:379 / 393
页数:15
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