Adjudin-preconditioned neural stem cells enhance neuroprotection after ischemia reperfusion in mice

• Published in: Stem cell research & therapy Vol. 8; no. 1; p. 248
• Main Authors: Zhang, Tingting, Yang, Xiao, Liu, Tengyuan, Shao, Jiaxiang, Fu, Ningzhen, Yan, Aijuan, Geng, Keyi, Xia, Weiliang
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 07-11-2017; BioMed Central; BMC
• Subjects: Adjudin; Animals; Blood–brain barrier; Brain Ischemia - therapy; Care and treatment; Hydrazines - pharmacology; Hydrazines - therapeutic use; Indazoles - pharmacology; Indazoles - therapeutic use; Inflammation; Ischemia; Mice; Neural stem cells; Neural Stem Cells - cytology; Neural Stem Cells - metabolism; Neuroprotection - genetics; Oxidative stress; Reperfusion Injury - metabolism; Risk factors; Stem cells; Stroke; Survival Analysis; Transplantation; China; Oxidative stress; Neural stem cells; Stroke; Inflammation; Adjudin; Blood–brain barrier
• ISSN: 1757-6512; 1757-6512
• DOI: 10.1186/s13287-017-0677-0

Transplantation of neural stem cells (NSCs) has been proposed as a promising therapeutic strategy for the treatment of ischemia/reperfusion (I/R)-induced brain injury. However, existing evidence has also challenged this therapy on its limitations, such as the difficulty for stem cells to survive after transplantation due to the unfavorable microenvironment in the ischemic brain. Herein, we have investigated whether preconditioning of NSCs with adjudin, a small molecule compound, could enhance their survivability and further improve the therapeutic effect for NSC-based stroke therapy.
We aimed to examine the effect of adjudin pretreatment on NSCs by measuring a panel of parameters after their transplantation into the infarct area of ipsilateral striatum 24 hours after I/R in mice.
We found that pretreatment of NSCs with adjudin could enhance the viability of NSCs after their transplantation into the stroke-induced infarct area. Compared with the untreated NSC group, the adjudin-preconditioned group showed decreased infarct volume and neurobehavioral deficiency through ameliorating blood-brain barrier disruption and promoting the expression and secretion of brain-derived neurotrophic factor. We also employed H
O
-induced cell death model in vitro and found that adjudin preconditioning could promote NSC survival through inhibition of oxidative stress and activation of Akt signaling pathway.
This study showed that adjudin could be used to precondition NSCs to enhance their survivability and improve recovery in the stroke model, unveiling the value of adjudin for stem cell-based stroke therapy.