Intracerebroventricular Transplantation of Human Mesenchymal Stem Cells Induced to Secrete Neurotrophic Factors Attenuates Clinical Symptoms in a Mouse Model of Multiple Sclerosis

被引:54
作者
Barhum, Yael [1 ]
Gai-Castro, Sharon [1 ]
Bahat-Stromza, Merav [1 ]
Barzilay, Ran [1 ]
Melamed, Eldad [1 ]
Offen, Daniel [1 ]
机构
[1] Tel Aviv Univ, Sackler Sch Med, Felsenstein Med Res Ctr, IL-49100 Petah Tiqwa, Israel
关键词
Multiple sclerosis (MS); Mesenchymal stem cells (MSCs); Experimental autoimmune encephalomyelitis (EAE); AUTOIMMUNE ENCEPHALOMYELITIS; STROMAL CELLS; GROWTH-FACTOR; REPAIR; NEUROPROTECTION; MIGRATION; IMMUNOMODULATION; EXPRESSION; INJECTION; CHEMOKINE;
D O I
10.1007/s12031-009-9302-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stem cell-based therapy holds great potential for future treatment of multiple sclerosis (MS). Bone marrow mesenchymal stem cells (MSCs) were previously reported to ameliorate symptoms in mouse MS models (experimental autoimmune encephalomyelitis, EAE). In this study, we induced MSCs to differentiate in vitro into neurotrophic factor-producing cells (NTFCs). Our main goal was to examine the clinical use of NTFCs on EAE symptoms. The NTFCs and MSCs were transplanted intracerebroventricularly (ICV) to EAE mice. We found that NTFCs transplantations resulted in a delay of symptom onset and increased animal survival. Transplantation of MSCs also exerted a positive effect but to a lesser extent. In vitro analysis demonstrated the NTFCs' capacity to suppress mice immune cells and protect neuronal cells from oxidative insult. Our results indicate that NTFCs-transplanted ICV delay disease symptoms of EAE mice, possibly via neuroprotection and immunomodulation, and may serve as a possible treatment to MS.
引用
收藏
页码:129 / 137
页数:9
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