Mesenchymal stem cells promote proliferation of endogenous neural stem cells and survival of newborn cells in a rat stroke model

被引:0
|
作者
Seung-Wan Yoo
Sung-Soo Kim
Soo-Yeol Lee
Hey-Sun Lee
Hyun-Soo Kim
Young-Don Lee
Haeyoung Suh-Kim
机构
[1] Ajou University School of Medicine,Department of Anatomy
[2] Suwon 443-749,Department of Molecular Science and Technology
[3] Korea.,Department of Hematology and Oncology
[4] Ajou University School of Medicine,Division of Cell Transformation and Restoration
[5] Suwon 443-749,Department of Biomedical Engineering
[6] Korea.,undefined
[7] Ajou University School of Medicine,undefined
[8] Suwon 443-749,undefined
[9] Korea.,undefined
[10] Center for Cell Death Regulating Biodrug,undefined
[11] Ajou University School of Medicine,undefined
[12] Suwon 443-749,undefined
[13] Korea.,undefined
[14] BK21,undefined
[15] Ajou University School of Medicine,undefined
[16] Suwon 443-749,undefined
[17] Korea.,undefined
[18] Brain Disease Research Center,undefined
[19] Ajou University School of Medicine,undefined
[20] Suwon 443-749,undefined
[21] Korea.,undefined
[22] Kyunghee University Youngin 446-701,undefined
[23] Korea.,undefined
来源
关键词
bromodeoxyuridine; doublecortin protein; mesenchymal stem cells; mesenchymal stem cell transplantation; stroke;
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学科分类号
摘要
Mesenchymal stem cells (MSCs) secrete bioactive factors that exert diverse responses in vivo. In the present study, we explored mechanism how MSCs may lead to higher functional recovery in the animal stroke model. Bone marrow-derived MSCs were transplanted into the brain parenchyma 3 days after induction of stroke by occluding middle cerebral artery for 2 h. Stoke induced proliferation of resident neural stem cells in subventricular zone. However, most of new born cells underwent cell death and had a limited impact on functional recovery after stroke. Transplantation of MSCs enhanced proliferation of endogenous neural stem cells while suppressing the cell death of newly generated cells. Thereby, newborn cells migrated toward ischemic territory and differentiated in ischemic boundaries into doublecortin+ neuroblasts at higher rates in animals with MSCs compared to control group. The present study indicates that therapeutic effects of MSCs are at least partly ascribed to dual functions of MSCs by enhancing endogenous neurogenesis and protecting newborn cells from deleterious environment. The results reinforce the prospects of clinical application using MSCs in the treatment of neurological disorders.
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页码:387 / 397
页数:10
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