scholarly journals Effects of acute versus post-acute systemic delivery of neural progenitor cells on neurological recovery and brain remodeling after focal cerebral ischemia in mice

2014 ◽  
Vol 5 (8) ◽  
pp. e1386-e1386 ◽  
Author(s):  
T R Doeppner ◽  
B Kaltwasser ◽  
M K Teli ◽  
E Bretschneider ◽  
M Bähr ◽  
...  
Circulation ◽  
2007 ◽  
Vol 116 (suppl_16) ◽  
Author(s):  
Soon-Tae Lee ◽  
Kon Chu ◽  
Keun-Hwa Jung ◽  
Hee-Kwon Park ◽  
Jeong-Min Kim ◽  
...  

Background and Objectives: Transplantation of neural progenitor cells (NPCs) has been studied to achieve the regeneration of damaged brain in experimental stroke models. Tissue ischemia induces systemic inflammatory activation, especially in spleen. However, the interaction between NPCs and immune/inflammatory cells has not been studied in ischemia models. In this study, we investigated whether NPC can attenuate cerebral and systemic inflammatory activation in focal cerebral ischemia. Methods: Focal cerebral ischemia was induced by intraluminal thread occlusion of the middle cerebral artery for 60 minutes (c57/bl6 adult male mice), and mouse NPC from primary neurosphere (1 million cells) or vehicle (PBS, control group) was injected via tail veins with cerebral reperfusion. Inflammatory cytokines were evaluated with RealTime-PCR at 22 hrs, and the weights of each spleen and thymus were measured. Results: Cerebral ischemia induced progressive atrophies of spleen and thymus when measured at 22 hr and 96 hr after ischemia. Intravenous injection of NPC accelerated these lymphoid organ atrophies, and the weights of spleen and thymus were significantly lower in NPC-injected mice at 96 hr after the ischemia compared to the vehicle injected mice. RealTime-PCR analysis using ischemic hemispheres and spleens showed reduced expressions of inflammatory cytokines, including TNF-alpha, IL-6, MIP-2, IL-13, FoxP3, IL-1beta, and IP10 in NPC-injected brains and spleens at 22 hr after the ischemia. Transplanted NPCs were detected in systemic organs, and mostly in spleen. NPC-injected mice showed reduced infarct volume and neurologic deficits. Conclusion: Intravenous transplantation of primary neuro-sphere cells in cerebral ischemia attenuated systemic inflammatory activation, which suggests that the immunomodulating property of neural progenitor cells can be applicable for preventing harmful inflammations after the tissue ischemia.


2008 ◽  
Vol 211 (1) ◽  
pp. 194-202 ◽  
Author(s):  
Nobuyuki Mochizuki ◽  
Norio Takagi ◽  
Koji Kurokawa ◽  
Chika Onozato ◽  
Yoshiyuki Moriyama ◽  
...  

2016 ◽  
Vol 54 (2) ◽  
pp. 1531-1540 ◽  
Author(s):  
Thorsten R. Doeppner ◽  
Viktorija Traut ◽  
Alexander Heidenreich ◽  
Britta Kaltwasser ◽  
Bert Bosche ◽  
...  

2009 ◽  
Vol 30 (3) ◽  
pp. 653-662 ◽  
Author(s):  
Lian Li ◽  
Quan Jiang ◽  
Guangliang Ding ◽  
Li Zhang ◽  
Zheng Gang Zhang ◽  
...  

We tested the hypotheses that administration routes affect the migration and distribution of grafted neural progenitor cells (NPCs) in the ischemic brain and that the ischemic lesion plays a role in mediating the grafting process. Male Wistar rats ( n=41) were subjected to 2-h middle cerebral artery occlusion (MCAo), followed 1 day later by administration of magnetically labeled NPCs. Rats with MCAo were assigned to one of three treatment groups targeted for cell transplantation intra-arterially (IA), intracisternally (IC), or intravenously (IV). MRI measurements consisting of T2-weighted imaging and three-dimensional (3D) gradient echo imaging were performed 24 h after MCAo, 4 h after cell injection, and once a day for 4 days. Prussian blue staining was used to identify the labeled cells, 3D MRI to detect cell migration and distribution, and T2 map to assess lesion volumes. Intra-arterial (IA) administration showed significantly increased migration, a far more diffuse distribution pattern, and a larger number of transplanted NPCs in the target brain than IC or IV administration. However, high mortality with IA delivery (IA: 41%; IC: 17%; IV: 8%) poses a serious concern for using this route of administration. Animals with smaller lesions at the time of transplantation have fewer grafted cells in the parenchyma.


2012 ◽  
Vol 3 (2) ◽  
pp. 43-53 ◽  
Author(s):  
Yoshiyuki Moriyama ◽  
Norio Takagi ◽  
Kanae Hashimura ◽  
Chisa Itokawa ◽  
Kouichi Tanonaka

2008 ◽  
Vol 368 (1) ◽  
pp. 151-156 ◽  
Author(s):  
Nobuyuki Mochizuki ◽  
Norio Takagi ◽  
Chika Onozato ◽  
Yoshiyuki Moriyama ◽  
Satoshi Takeo ◽  
...  

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