Comparative study of the neural differentiation capacity of mesenchymal stromal cells from different tissue sources: An approach for their use in neural regeneration therapies
Journal
PLOS ONE
ISSN
1932-6203
Date Issued
2019
Author(s)
Daniela N. Urrutia
Pablo Caviedes
Rodrigo Mardones
José J. Minguell
ANA MARIA FERNANDA VEGA LETTER
Claudio M. Jofre
Type
Resource Types::text::journal::journal article
URL Institutional Repository
Cite this document
Urrutia, D. N., Caviedes, P., Mardones, R., Minguell, J. J., Vega-Letter, A. M., & Jofre, C. M. (2019). Comparative study of the neural differentiation capacity of mesenchymal stromal cells from different tissue sources: An approach for their use in neural regeneration therapies. PLOS ONE, 14(3), e0213032. https://doi.org/10.1371/journal.pone.0213032
Subjects
human bone-marrow
;
stem-cells
;
progenitor cells
;
adipose-tissue
;
rat model
;
in-vitro
;
expression
;
transplantation
;
populations
;
precursors
;
adipose tissue
;
adult
;
bone marrow cells
;
cell proliferation
;
cell- and tissue-based therapy
;
cells, cultured
;
central nervous system diseases
;
chile
;
female
;
humans
;
male
;
mesenchymal stem cells
;
nerve regeneration
;
neurogenesis
;
primary cell culture
;
regenerative medicine
;
skin
;
umbilical cord
;
young adult
;
5' nucleotidase
;
beta tubulin
;
beta1 integrin
;
cd11b antigen
;
cd19 antigen
;
cd34 antigen
;
cell marker
;
cell protein
;
disks large homolog 4
;
endoglin
;
hla dr antigen
;
messenger rna
;
nestin
;
neurotrophin 3
;
nuclear receptor related factor 1
;
protein nefl
;
protein nefm
;
protein s100b
;
receptor type tyrosine protein phosphatase c
;
synaptophysin
;
thy 1 membrane glycoprotein
;
tyrosine 3 monooxygenase
;
unclassified drug
;
adipogenesis
;
adipose tissue
;
adult
;
article
;
bone development
;
bone marrow
;
cell count
;
cell expansion
;
cell function
;
cell isolation
;
cell lineage
;
cell maturation
;
cell population
;
cell proliferation
;
cell selection
;
cell size
;
cell structure
;
cell therapy
;
cell transdifferentiation
;
cellular distribution
;
chondrogenesis
;
comparative study
;
controlled study
;
degenerative disease
;
ex vivo study
;
feasibility study
;
female
;
flow cytometry
;
gene
;
gene expression
;
human
;
human cell
;
human tissue
;
immunophenotyping
;
male
;
mesenchymal stem cell
;
mesenchymal stroma cell
;
nefl gene
;
nefm gene
;
nerve cell differentiation
;
nerve regeneration
;
nervous system development
;
neural stem cell
;
neurite outgrowth
;
neurofilament
;
newborn
;
nt 3 gene
;
nurr1 gene
;
protein expression
;
s100b gene
;
skin
;
spindle cell
;
synapse vesicle
;
tissue differentiation
;
tissue distribution
;
umbilical cord
;
biological therapy
;
bone marrow cell
;
cell culture
;
central nervous system disease
;
chile
;
cytology
;
nervous system development
;
physiology
;
primary cell culture
;
procedures
;
regenerative medicine
;
young adult