scholarly journals Cytosolic phospholipase A 2 protein as a novel therapeutic target for spinal cord injury

2014 ◽  
Vol 75 (5) ◽  
pp. 644-658 ◽  
Author(s):  
Nai‐Kui Liu ◽  
Ling‐Xiao Deng ◽  
Yi Ping Zhang ◽  
Qing‐Bo Lu ◽  
Xiao‐Fei Wang ◽  
...  
2011 ◽  
Vol 25 (12) ◽  
pp. 4240-4252 ◽  
Author(s):  
Rubèn López‐Vales ◽  
Nader Ghasemlou ◽  
Adriana Redensek ◽  
Bradley J. Kerr ◽  
Efrosini Barbayianni ◽  
...  

2014 ◽  
Vol 34 (6) ◽  
pp. 519-526 ◽  
Author(s):  
Anandakumar Shunmugavel ◽  
Mushfiquddin Khan ◽  
Francis M. Hughes ◽  
J. Todd Purves ◽  
Avtar Singh ◽  
...  

2006 ◽  
Vol 169 (3) ◽  
pp. 1039-1047 ◽  
Author(s):  
Fei Qiao ◽  
Carl Atkinson ◽  
Hongbin Song ◽  
Ravinder Pannu ◽  
Inderjit Singh ◽  
...  

2008 ◽  
Vol 24 (4-5) ◽  
pp. 239-250 ◽  
Author(s):  
Jean R. Wrathall ◽  
Judith M. Lytle

Traumatic injury to the adult spinal cord results in a massive loss of cells and permanent functional deficits. However, recent studies demonstrate that there is a proliferative response of endogenous glial precursors and progenitors and perhaps also pluripotent neural stem cells. These cells may prove to be an important new therapeutic target to improve recovery after injury to the spinal cord and brain.


2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Jinsong Wei ◽  
Jiafeng Wang ◽  
Yulan Zhou ◽  
Shouquan Yan ◽  
Keshen Li ◽  
...  

MicroRNA-146a participates in spinal cord injury (SCI) recovery. Until recently, how miRNA-146a participates in SCI remained unclear. In this study, we tried to explore the roles of miRNA-146a in the recovery of SCI using a rat model. The expression of the probable target genes of miRNA-146a (including IRAK1 and TARF6) as well as proinflammation cytokines were measured until 7 days after surgery in the three groups (sham group, SCI group, and miRNA-146a antagomir injection group). Also, the animals’ motivations were estimated using Basso Beattie Bresnahan (BBB) during the whole experiment. A luciferase assay was performed to demonstrate that miRNA-146a could directly target the mRNAs of IRAK1 and TRAF6. Our experiments indicate that miRNA-146a inhibits proinflammatory cytokine secretion by suppressing IRAK1 and TRAF6 expression in the SCI model. In contrast, miRNA-146a may be upregulated by inflammatory mediators via the IRAK1/TRAF6 pathway in the spinal cord. As a negative feedback element, miRNA-146a could make sure that the expression of IRAK1- and TRAF6-mediated genes was under tight control. Thus, miRNA-146a may serve as a novel therapeutic target for SCI interventions.


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