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Massive clonal selection and transiently contributing clones during expansion of mesenchymal stem cell cultures revealed by lentiviral RGB-barcode technology

 
: Selich, Anton; Daudert, Jannik; Hass, Ralf; Philipp, Friederike; Kaisenberg, Constantin von; Paul, Gabi; Cornils, Kerstin; Fehse, Boris; Rittinghausen, Susanne; Schambach, Axel; Rothe, Michael

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Stem cells translational medicine : SCTM 5 (2016), No.5, pp.591-601
ISSN: 2157-6564
ISSN: 2157-6580
European Commission EC
FP7-HEALTH; 261387; CELL-PID
Advanced Cell-based Therapies for the treatment of Primary ImmunoDeficiency
English
Journal Article
Fraunhofer ITEM ()
mesenchymal stem cells; umbilical cord; clonal evolution; DNA barcoding; reproducibility of results; stem cell niche

Abstract
Mesenchymal stem (or stromal) cells (MSCs) have been used in more than 400 clinical trials for the treatment of various diseases. The clinical benefit and reproducibility of results, however, remain extremely variable. During the in vitro expansion phase, which is necessary to achieve clinically relevant cell numbers, MSCs show signs of aging accompanied by different contributions of single clones to the mass culture. Here we used multicolor lentiviral barcode labeling to follow the clonal dynamics during in vitro MSC expansion from whole umbilical cord pieces (UCPs). The clonal composition was analyzed by a combination of flow cytometry, fluorescence microscopy, and deep sequencing. Starting with highly complex cell populations, we observed a massive reduction in diversity, transiently dominating populations, and a selection of single clones over time. Importantly, the first wave of clonal constriction already occurred in the early passages during MSC expansion. Consecutive MSC cultures from the same UCP implied the existence of more primitive, MSC culture-initiating cells. Our results show that microscopically homogenous MSC mass cultures consist of many subpopulations, which undergo clonal selection and have different capabilities. Among other factors, the clonal composition of the graft might have an impact on the functional properties of MSCs in experimental and clinical settings.

: http://publica.fraunhofer.de/documents/N-404296.html