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Isolating Pediatric Mesenchymal Stem Cells with Enhanced Expansion and Differentiation Capabilities
Author(s) -
Callie Knuth,
Caoimhe H. Kiernan,
Virginia Palomares Cabeza,
Johannes Lehmann,
Janneke WitteBouma,
Derk ten Berge,
Pieter A.J. Brama,
Eppo B. Wolvius,
Elske M. Strabbing,
Maarten J. Koudstaal,
Roberto Narcisi,
Eric Farrell
Publication year - 2018
Publication title -
tissue engineering part c methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.846
H-Index - 70
eISSN - 1937-3392
pISSN - 1937-3384
DOI - 10.1089/ten.tec.2018.0031
Subject(s) - mesenchymal stem cell , bone marrow , stem cell , microbiology and biotechnology , cellular differentiation , biology , immunology , genetics , gene
Mesenchymal stem cells/marrow stromal cells (MSCs) are attractive for applications ranging from research and development to use in clinical therapeutics. However, the most commonly studied MSCs, adult bone marrow MSCs (A-MSCs), are limited by significant donor variation resulting in inconsistent expansion rates and multilineage differentiation capabilities. We have recently obtained permission to isolate pediatric MSCs (P-MSCs) from surplus iliac crest bone chips. Here, we developed a simple and easily replicable isolation protocol yielding P-MSCs, which adhere to MSC defining guidelines. After confirming immunophenotypic marker expression, we compared expansion rates, senescence, morphology, and trilineage differentiation of P-MSCs to A-MSCs for multiple donors. We found P-MSCs have faster in vitro replication, consistently show significantly lower senescence, and are capable of more reproducible multilineage differentiation than A-MSCs. We, therefore, believe P-MSCs are a promising candidate for use in research applications and potentially as part of an allogeneic therapeutic treatment.

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