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Human Wharton's Jelly-Derived Stem Cells Display a Distinct Immunomodulatory and Proregenerative Transcriptional Signature Compared to Bone Marrow-Derived Stem Cells.

Authors :
Donders R
Bogie JFJ
Ravanidis S
Gervois P
Vanheusden M
Marée R
Schrynemackers M
Smeets HJM
Pinxteren J
Gijbels K
Walbers S
Mays RW
Deans R
Van Den Bosch L
Stinissen P
Lambrichts I
Gyselaers W
Hellings N
Source :
Stem cells and development [Stem Cells Dev] 2018 Jan 15; Vol. 27 (2), pp. 65-84. Date of Electronic Publication: 2017 Dec 21.
Publication Year :
2018

Abstract

Mesenchymal stromal cells (MSCs) are multipotent stem cells with immunosuppressive and trophic support functions. While MSCs from different sources frequently display a similar appearance in culture, they often show differences in their surface marker and gene expression profiles. Although bone marrow is considered the "gold standard" tissue to isolate classical MSCs (BM-MSC), MSC-like cells are currently also derived from more easily accessible extra-embryonic tissues such as the umbilical cord. In this study, we defined the best way to isolate MSCs from the Wharton's jelly of the human umbilical cord (WJ-MSC) and assessed the mesenchymal and immunological phenotype of BM-MSC and WJ-MSC. Moreover, the gene expression profile of established WJ-MSC cultures was compared to two different bone marrow-derived stem cell populations (BM-MSC and multipotent adult progenitor cells or MAPC <superscript>®</superscript> ). We observed that explant culturing of Wharton's jelly matrix is superior to collagenase tissue digestion for obtaining mesenchymal-like cells, with explant isolated cells displaying increased expansion potential. While being phenotypically similar to adult MSCs, WJ-MSC show a different gene expression profile. Gene ontology analysis revealed that genes associated with cell adhesion, proliferation, and immune system functioning are enriched in WJ-MSC. In vivo transplantation confirms their immune modulatory effect on T cells, similar to BM-MSC and MAPC. Furthermore, WJ-MSC intrinsically overexpress genes involved in neurotrophic support and their secretome induces neuronal maturation of SH-SY5Y neuroblastoma cells to a greater extent than BM-MSC. This signature makes WJ-MSC an attractive candidate for cell-based therapy in neurodegenerative and immune-mediated central nervous system disorders such as multiple sclerosis, Parkinson's disease, or amyotrophic lateral sclerosis.

Details

Language :
English
ISSN :
1557-8534
Volume :
27
Issue :
2
Database :
MEDLINE
Journal :
Stem cells and development
Publication Type :
Academic Journal
Accession number :
29267140
Full Text :
https://doi.org/10.1089/scd.2017.0029