2011
DOI: 10.1016/j.brainres.2011.05.055
|View full text |Cite
|
Sign up to set email alerts
|

Human umbilical mesenchymal stem cells enhance the expression of neurotrophic factors and protect ataxic mice

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

3
51
2

Year Published

2012
2012
2017
2017

Publication Types

Select...
6
2

Relationship

1
7

Authors

Journals

citations
Cited by 77 publications
(56 citation statements)
references
References 38 publications
3
51
2
Order By: Relevance
“…However, the efficacy of hUC-MSCs on ataxic mice was related to their release of neuronal growth factors, not differentiation into neuronal cells [21]. This study showed that hUC-MSCs exerted immune modulatory effects by inducing a shift of T cells from Th1 proinflammatory cells to Th2 anti-inflammatory cells.…”
Section: Stem Cells Treatment For Eaementioning
confidence: 71%
See 1 more Smart Citation
“…However, the efficacy of hUC-MSCs on ataxic mice was related to their release of neuronal growth factors, not differentiation into neuronal cells [21]. This study showed that hUC-MSCs exerted immune modulatory effects by inducing a shift of T cells from Th1 proinflammatory cells to Th2 anti-inflammatory cells.…”
Section: Stem Cells Treatment For Eaementioning
confidence: 71%
“…Our previous study verified that hUC-MSCs can cross the blood-brain barrier via intravenous transplantation [21]. However, the efficacy of hUC-MSCs on ataxic mice was related to their release of neuronal growth factors, not differentiation into neuronal cells [21].…”
Section: Stem Cells Treatment For Eaementioning
confidence: 95%
“…Brain implanted marrow stromal cells also differentiate into glial cells [25] . Importantly, grafting MSCs in several brain lesion models reduces neuronal deficits [35][36][37][38][39][40][41][42] . However, current evidence suggests that in the experimental models used, the repair and functional improvements reported are primarily mediated by paracrine or cell-cell interactions rather than by the successful engraftment and the in situ transdifferentiation of implanted MSCs into neural cells [43][44][45][46][47] .…”
Section: Artifactsmentioning
confidence: 99%
“…Instead, trophic factors released from MSCs might act on neurons because hepatocyte growth factor (HGF), fibroblast growth factor-2 (FGF-2), insulin-like growth factor-1 (IGF-1), and vascular endothelial growth factor (VEGF) have all been detected in MSC-conditioned medium [30]. Indeed, human umbilical MSC-treated mice showed higher levels of IGF-1 and VEGF in the cerebellum and peripheral blood circulation in ataxic mice induced by cytosine beta-D-arabinofuranoside [28]. The extracellular matrix molecules produced by MSCs have also been shown to support neural cell attachment, growth, and axonal extension [36].…”
Section: Actions Of Administered Mscs On Neuronsmentioning
confidence: 96%
“…The first attempt was to use pharmacologically induced ataxic animals. Ataxic mice were induced by cytosine beta-D-arabinofuranoside, after which human umbilical MSCs were injected into these mice [28]. The ataxic mice were given an intravenous injection of 2 × 10 6 human umbilical MSCs once a week for three consecutive weeks.…”
Section: Efficacy Of Mscs In Treating Mouse Models For Cerebellar Ataxiamentioning
confidence: 99%