A promising approach for musculoskeletal repair and regeneration is mesenchymal-stem-cell- (MSC-)based tissue engineering. The aim of the study was to apply a simple protocol based on mincing the umbilical cord (UC), without removing any blood vessels or using any enzymatic digestion, to rapidly obtain an adequate number of multipotent UC-MSCs. We obtained, at passage 1 (P1), a mean value of 4,2 × 10 6 cells (SD 0,4) from each UC. At immunophenotypic characterization, cells were positive for CD73, CD90, CD105, CD44, CD29, and HLA-I and negative for CD34 and HLA-class II, with a subpopulation negative for both HLA-I and HLA-II. Newborn origin and multilineage potential toward bone, fat, cartilage, and muscle was demonstrated. Telomere length was similar to that of bone-marrow (BM) MSCs from young donors. The results suggest that simply collecting UC-MSCs at P1 from minced umbilical cord fragments allows to achieve a valuable population of cells suitable for orthopaedic tissue engineering. Copyright © 2012 A. Marmotti et al.
CITATION STYLE
Marmotti, A., Mattia, S., Bruzzone, M., Buttiglieri, S., Risso, A., Bonasia, D. E., … Peretti, G. M. (2012). Minced umbilical cord fragments as a source of cells for orthopaedic tissue engineering: An in vitro study. Stem Cells International. https://doi.org/10.1155/2012/326813
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