scholarly journals TNF-α induces human neural progenitor cell survival after oxygen–glucose deprivation by activating the NF-κB pathway

2018 ◽  
Vol 50 (4) ◽  
Author(s):  
Miri Kim ◽  
Kwangsoo Jung ◽  
Il-Sun Kim ◽  
Il-Shin Lee ◽  
Younhee Ko ◽  
...  
2020 ◽  
Vol 14 ◽  
Author(s):  
Jixian Wang ◽  
Brian Wang ◽  
Lei Jiang ◽  
Kaijing Zhou ◽  
Guo-Yuan Yang ◽  
...  

Author(s):  
Lin Zhang ◽  
Irina Graf ◽  
Yaoyun Kuang ◽  
Xuan Zheng ◽  
Matteo Haupt ◽  
...  

Objective: Extracellular vesicles (EVs) derived from neural progenitor cells enhance poststroke neurological recovery, albeit the underlying mechanisms remain elusive. Since previous research described an enhanced poststroke integrity of the blood-brain barrier (BBB) upon systemic transplantation of neural progenitor cells, we examined if neural progenitor cell-derived EVs affect BBB integrity and which cellular mechanisms are involved in the process. Approach and Results: Using in vitro models of primary brain endothelial cell (EC) cultures as well as co-cultures of brain ECs (ECs) and astrocytes exposed to oxygen glucose deprivation, we examined the effects of EVs or vehicle on microvascular integrity. In vitro data were confirmed using a mouse transient middle cerebral artery occlusion model. Cultured ECs displayed increased ABCB1 (ATP-binding cassette transporter B1) levels when exposed to oxygen glucose deprivation, which was reversed by treatment with EVs. The latter was due to an EV-induced inhibition of the NF-κB (nuclear factor-κB) pathway. Using a BBB co-culture model of ECs and astrocytes exposed to oxygen glucose deprivation, EVs stabilized the BBB and ABCB1 levels without affecting the transcellular electrical resistance of ECs. Likewise, EVs yielded reduced Evans blue extravasation, decreased ABCB1 expression as well as an inhibition of the NF-κB pathway, and downstream matrix metalloproteinase 9 (MMP-9) activity in stroke mice. The EV-induced inhibition of the NF-κB pathway resulted in a poststroke modulation of immune responses. Conclusions: Our findings suggest that EVs enhance poststroke BBB integrity via ABCB1 and MMP-9 regulation, attenuating inflammatory cell recruitment by inhibition of the NF-κB pathway.


Stem Cells ◽  
2012 ◽  
Vol 30 (11) ◽  
pp. 2571-2583 ◽  
Author(s):  
Bing Zhu ◽  
Dongsheng Xu ◽  
Xiaobei Deng ◽  
Qiang Chen ◽  
Yunlong Huang ◽  
...  

2009 ◽  
pp. NA-NA ◽  
Author(s):  
Julia C. Knight ◽  
Eugene L. Scharf ◽  
Yang Mao-Draayer

PROTEOMICS ◽  
2019 ◽  
Vol 19 (3) ◽  
pp. 1970011
Author(s):  
Melissa K. Jones ◽  
Bin Lu ◽  
Dawn Zhaohui Chen ◽  
Weston R. Spivia ◽  
Augustus T. Mercado ◽  
...  

2014 ◽  
Vol 134 (5) ◽  
pp. 441-447 ◽  
Author(s):  
Fredrik Edin ◽  
Wei Liu ◽  
Marja Boström ◽  
Peetra U. Magnusson ◽  
Helge Rask-Andersen

Author(s):  
Orianne Mazemondet ◽  
Rayk Hubner ◽  
Jana Frahm ◽  
Dirk Koczan ◽  
Benjamin Bader ◽  
...  

AbstractReNcell VM is an immortalized human neural progenitor cell line with the ability to differentiate in vitro into astrocytes and neurons, in which the Wnt/β-catenin pathway is known to be involved. However, little is known about kinetic changes of this pathway in human neural progenitor cell differentiation. In the present study, we provide a quantitative profile of Wnt/β-catenin pathway dynamics showing its spatio-temporal regulation during ReNcell VM cell differentiation. We show first that T-cell factor dependent transcription can be activated by stabilized β-catenin. Furthermore, endogenous Wnt ligands, pathway receptors and signaling molecules are temporally controlled, demonstrating changes related to differentiation stages. During the first three hours of differentiation the signaling molecules LRP6, Dvl2 and β-catenin are spatio-temporally regulated between distinct cellular compartments. From 24 h onward, components of the Wnt/β-catenin pathway are strongly activated and regulated as shown by mRNA up-regulation of Wnt ligands (Wnt5a and Wnt7a), receptors including Frizzled-2, -3, -6, -7, and -9, and co-receptors, and target genes including Axin2. This detailed temporal profile of the Wnt/β-catenin pathway is a first step to understand, control and to orientate, in vitro, human neural progenitor cell differentiation.


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