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Wharton's jelly-derived mesenchymal cells as a new source for the generation of microtissues for tissue engineering applications.
Durand-Herrera, D; Campos, F; Jaimes-Parra, B D; Sánchez-López, J D; Fernández-Valadés, R; Alaminos, M; Campos, A; Carriel, V.
Affiliation
  • Durand-Herrera D; Department of Histology, Tissue Engineering Group, University of Granada, Granada, Spain.
  • Campos F; Doctoral Programme in Biomedicine, University of Granada, Granada, Spain.
  • Jaimes-Parra BD; Instituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
  • Sánchez-López JD; Department of Histology, Tissue Engineering Group, University of Granada, Granada, Spain.
  • Fernández-Valadés R; Instituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
  • Alaminos M; Department of Histology, Tissue Engineering Group, University of Granada, Granada, Spain.
  • Campos A; Division of Maxillofacial Surgery, University Hospital Complex of Granada, Granada, Spain.
  • Carriel V; Instituto de Investigación Biosanitaria ibs.GRANADA, Granada, Spain.
Histochem Cell Biol ; 150(4): 379-393, 2018 Oct.
Article in En | MEDLINE | ID: mdl-29931444
ABSTRACT
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 28 days. 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 4-21 days 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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tissue Engineering / Wharton Jelly / Mesenchymal Stem Cells Limits: Humans Language: En Journal: Histochem Cell Biol Journal subject: CITOLOGIA / HISTOCITOQUIMICA Year: 2018 Type: Article Affiliation country: Spain

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tissue Engineering / Wharton Jelly / Mesenchymal Stem Cells Limits: Humans Language: En Journal: Histochem Cell Biol Journal subject: CITOLOGIA / HISTOCITOQUIMICA Year: 2018 Type: Article Affiliation country: Spain