Bone marrow-derived mesenchymal stem cells reduce brain amyloid-β deposition and accelerate the activation of microglia in an acutely induced Alzheimer's disease mouse model

被引:164
作者
Lee, Jong Kil [2 ,3 ]
Jin, Hee Kyung [2 ,3 ]
Bae, Jae-sung [1 ,3 ]
机构
[1] Kyungpook Natl Univ, Sch Med & Brain Korea 21, Dept Physiol, Lab Alzheimers Dis & Stem Cell, Taegu 700422, South Korea
[2] Kyungpook Natl Univ, Coll Vet Med, Dept Lab Anim Med, Taegu 700422, South Korea
[3] Kyungpook Natl Univ, Stem Cell Neuroplast Res Grp, Taegu 700422, South Korea
关键词
Acutely induced Alzheimer's disease model; Bone marrow-derived mesenchymal stem cell; Amyloid-beta; Microglia; Transplantation; SYNAPTIC-TRANSMISSION; STROMAL CELLS; MICE; TRANSPLANTATION; PEPTIDE; NEURODEGENERATION; NEUROPROTECTION; PHAGOCYTOSIS; MECHANISMS; CLEARANCE;
D O I
10.1016/j.neulet.2008.11.059
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
The therapeutic potential of bone marrow-derived mesenchymal stem cells (BM-MSCs) has recently been explored in various pathological conditions of the central nervous system (CNS). However, the application of BM-MSCs in acutely induced Alzheimer's disease (AD) has not yet been reported. Herein the feasibility of using the BM-MSCs, as a therapeutic agent for AD has been tested. To assess this possibility, an acutely induced AD model induced by injecting amyloid-beta (A beta) into the dentate gyrus (DG) of hippocampus of C57BL/6 mice was used. Intracerebral transplantation of BM-MSCs into the brain of an induced AD model reduced their A beta levels when compared to sham-transplanted animals. The diminution of A beta deposits was accompanied by the activation of microglia. In addition, the activated microglia was located near the A beta deposits, and their morphology was changed from ramified to ameboid as a sign of microglial phagocytosis. This study provides evidence that BM-MSCs can promote the reduction of A beta through the microglial activation in this acutely induced AD brain, suggesting a potential therapeutic agent against AD. (C) 2008 Elsevier Ireland Ltd. All rights reserved
引用
收藏
页码:136 / 141
页数:6
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