NFL-lipid nanocapsules for brain neural stem cell targeting in vitro and in vivo

2016 ◽  
Vol 238 ◽  
pp. 253-262 ◽  
Author(s):  
Dario Carradori ◽  
Patrick Saulnier ◽  
Véronique Préat ◽  
Anne des Rieux ◽  
Joel Eyer
2014 ◽  
Vol 175 ◽  
pp. 13-26 ◽  
Author(s):  
Yung-Kang Peng ◽  
Cathy N. P. Lui ◽  
Tsen-Hsuan Lin ◽  
Chen Chang ◽  
Pi-Tai Chou ◽  
...  

Neural stem cells (NSCs), which generate the main phenotypes of the nervous system, are multipotent cells and are able to differentiate into multiple cell types via external stimuli from the environment. The extraction, modification and re-application of NSCs have thus attracted much attention and raised hopes for novel neural stem cell therapies and regenerative medicine. However, few studies have successfully identified the distribution of NSCs in a live brain and monitored the corresponding extraction processes both in vitro and in vivo. To address those difficulties, in this study multi-functional uniform nanoparticles comprising an iron oxide core and a functionalized silica shell (Fe3O4@SiO2(FITC)-CD133, FITC: a green emissive dye, CD133: anti-CD133 antibody) have been strategically designed and synthesized for use as probe nanocomposites that provide four-in-one functionality, i.e., magnetic agitation, dual imaging (both magnetic resonance and optical) and specific targeting. It is shown that these newly synthesized Fe3O4@SiO2(FITC)-CD133 particles have clearly demonstrated their versatility in various applications. (1) The magnetic core enables magnetic cell collection and T2 magnetic resonance imaging. (2) The fluorescent FITC embedded in the silica framework enables optical imaging. (3) CD133 anchored on the outermost surface is demonstrated to be capable of targeting neural stem cells for cell collection and bimodal imaging.


2014 ◽  
Vol 54 (2) ◽  
pp. 199-210 ◽  
Author(s):  
Peng Zhang ◽  
Cuiying Wu ◽  
Ning Liu ◽  
Lijun Niu ◽  
Zhongjie Yan ◽  
...  

2020 ◽  
Vol 1735 ◽  
pp. 146717
Author(s):  
Jiyeon K. Denninger ◽  
Xi Chen ◽  
Altan M. Turkoglu ◽  
Patricia Sarchet ◽  
Abby R. Volk ◽  
...  

2014 ◽  
Vol 5 (4) ◽  
pp. 100 ◽  
Author(s):  
Joerg Hucklenbroich ◽  
Rebecca Klein ◽  
Bernd Neumaier ◽  
Rudolf Graf ◽  
Gereon Fink ◽  
...  

Cell Research ◽  
2007 ◽  
Vol 17 (1) ◽  
pp. 56-61 ◽  
Author(s):  
Ana I Teixeira ◽  
Joshua K Duckworth ◽  
Ola Hermanson

STEMedicine ◽  
2020 ◽  
Vol 1 (3) ◽  
pp. e59
Author(s):  
Ziyun Jiang ◽  
Mingliang Tang

Background: Ischemic stroke is the most common cause of ischemia-related death globally. Brain injuries due to stroke and trauma are typically followed by inflammation reactions within the central nervous system (CNS). Neural stem cell (NSC)-based therapeutic strategies show great potential for treating stroke and ischemia-mediated brain injuries, and migration of NSCs is a critical step involved in NSC-based therapy. Methods: In order to examine the effects of microglial activation upon ischemia and stroke on NSC behaviors, oxygen-glucose deprivation (OGD) in vitro model was established for mimicking in vivo stroke and ischemia pathological conditions in this study. By combining of enzyme-linked immunosorbent assay, migration assay, Western blot and immunostaining, we found that OGD insult induced microglial activation by releasing cytokines and chemokines. Results: The conditioned media (CM) of OGD-treated groups impaired the proliferation and capability of neurosphere formation. Moreover, we found the stromal cell-derived factor 1α/CXC chemokine receptor 4 (CXCR4) pathway was an active player that facilitated the migration of NSCs, since a CXCR4 specific antagonist AMD3100 was able to impair NSC migration both in vitro and in vivo. Conclusion: The current study presents a potential interaction between NSC behaviors and microglial activation underlying brain injuries, such as ischemia and stroke. More importantly, we reveal the underlying mechanisms of microglia-induced NSC migration under OGD conditions and it should be beneficial to stem cell-based therapies to treat acute brain injuries.


2021 ◽  
Author(s):  
Fabrizio Favaloro ◽  
Annina DeLeo ◽  
Ana Delgado ◽  
Fiona Doetsch

In the adult mouse brain, neural stem cells (NSCs) in the ventricular-subventricular zone (V-SVZ) generate neurons and glia throughout life. microRNAs are important regulators of cell states, frequently acting in a stage- or context-dependent manner. Here, miRNA profiling of FACS-purified populations identified miR-17~92 as highly upregulated in activated NSCs and transit amplifying cells (TACs) in comparison to quiescent NSCs. Conditional deletion of miR-17~92 in NSCs reduced stem cell proliferation both in vitro and in vivo. In contrast, in TACs, miR-17~92 deletion caused a selective shift from neurogenic DLX2+ TACs towards oligodendrogenic OLIG2+ TACs, resulting in increased oligodendrogenesis to the corpus callosum. miR-17~92 deletion also decreased proliferation and maturation of intraventricular oligodendrocyte progenitor cells. Together, these findings reveal stage- and cell-type- specific functions of the miR-17~92 cluster within adult V-SVZ neural stem cell lineages.


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