scholarly journals Getting the right stuff: Controlling neural stem cell state and fate in vivo and in vitro with biomaterials

Cell Research ◽  
2007 ◽  
Vol 17 (1) ◽  
pp. 56-61 ◽  
Author(s):  
Ana I Teixeira ◽  
Joshua K Duckworth ◽  
Ola Hermanson
2018 ◽  
Vol 32 (23-24) ◽  
pp. 1550-1561 ◽  
Author(s):  
Hideyuki Komori ◽  
Krista L. Golden ◽  
Taeko Kobayashi ◽  
Ryoichiro Kageyama ◽  
Cheng-Yu Lee

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 ◽  
...  

2016 ◽  
Vol 238 ◽  
pp. 253-262 ◽  
Author(s):  
Dario Carradori ◽  
Patrick Saulnier ◽  
Véronique Préat ◽  
Anne des Rieux ◽  
Joel Eyer

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

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.


Author(s):  
Satish Kumar Tiwari ◽  
Sudip Mandal

Over the years, Drosophila has served as a wonderful genetically tractable model system to unravel various facets of tissue-resident stem cells in their microenvironment. Studies in different stem and progenitor cell types of Drosophila have led to the discovery of cell-intrinsic and extrinsic factors crucial for stem cell state and fate. Though initially touted as the ATP generating machines for carrying various cellular processes, it is now increasingly becoming clear that mitochondrial processes alone can override the cellular program of stem cells. The last few years have witnessed a surge in our understanding of mitochondria’s contribution to governing different stem cell properties in their subtissular niches in Drosophila. Through this review, we intend to sum up and highlight the outcome of these in vivo studies that implicate mitochondria as a central regulator of stem cell fate decisions; to find the commonalities and uniqueness associated with these regulatory mechanisms.


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