Publication: Seven days post-injury fate and effects of genetically labelled adipose-derived mesenchymal cells on a rat traumatic brain injury experimental model
Authors
Dori, Ioanna ; Petrakis, Spyros ; Giannakopoulou, Aggeliki ; Bekiari, Chryssa ; Grivas, Ioannis ; Siska, Evangelia K. ; Koliakos, Georgios ; Papadopoulos, Georgios C.
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-11-864
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info:eu-repo/semantics/article
Description
Abstract
Mesenchymal stromal cells (MSC) have been
suggested to have beneficial effects on animal models of
traumatic brain injury (TBI), owing to their neurotrophic
and immunomodulatory properties. Adipose tissuederived stromal cells (ASCs) are multipotent MSC that
can be harvested with minimally invasive methods, show
a high proliferative capacity, low immunogenicity if
allogeneic, and can be used in autologous or
heterologous settings. In the present study ASCs were
genetically labelled using the Sleeping Beauty
transposon to express the fluorescent protein Venus.
Venus+ASCs were transplanted intra-cerebroventricularly (ICV), on a rat TBI model and their
survival, fate and effects on host brain responses were
examined at seven days post-injury (7dPI). We provide
evidence that Venus+ASCs survived, migrated into the
periventricular striatum and were negative for neuronal
or glial lineage differentiation markers. Venus+ASCs
stimulated the proliferation of endogenous neural stem
cells (NSCs) in the brain neurogenic niches, the
subventricular zone (SVZ) and the hippocampal dentate
gyrus (DG). It was also evident that Venus+ASCs
modify the host brain’s cellular microenvironment both
at the injury site and at their localization area by
promoting a significant reduction of the lesion area, as
well as altering the post-injury, pro-inflammatory profile
of microglial and astrocytic cell populations. Our data
support the view that ICV transplantation of ASCs
induces alterations in the host brain’s cellular response to
injury that may be correlated to a reversal from a
detrimental to a beneficial state which is permissive for
regeneration and repair.
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Citation
Histology and Histopathology, Vol.32, nº10, (2017)
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