Loss of RE-1 silencing factor in mesenchymal stem cell-derived dopamine progenitors induces functional maturity

被引:43
作者
Trzaska, Katarzyna A. [1 ,2 ]
Reddy, Bobby Y. [1 ,2 ]
Munoz, Jessian L. [4 ]
Li, Ke-Yong [3 ]
Ye, Jiang-Hong [3 ]
Rameshwar, Pranela [1 ]
机构
[1] Univ Med & Dent New Jersey, Dept Med Hematol Oncol, New Jersey Med Sch, Newark, NJ 07103 USA
[2] Univ Med & Dent New Jersey, Grad Sch Biomed Sci, New Jersey Med Sch, Newark, NJ 07103 USA
[3] Univ Med & Dent New Jersey, New Jersey Med Sch, Dept Anesthesiol, Newark, NJ 07103 USA
[4] Univ Puerto Rico Cayey, Dept Biol, Cayey, PR USA
关键词
REST/NRSF; Dopamine; Mesenchymal stem cells; Neural repair;
D O I
10.1016/j.mcn.2008.07.006
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Stem cell-derived dopamine (DA) neurons hold great promise for Parkinson's disease (PD). Mesenchymal stein cells (MSCs) have great potential for clinical applications. The generation of DA cells from MSCs using sonic hedgehog (SHH) and fibroblast growth factors (FGF8 and bFGF) has been reported. However, the DA cells showed weak electrical properties, representing DA neuron progenitors. Since RE-I Silencing Factor (REST), suppresses mature neuronal genes in neuronal progenitors, we Studied its role in the maturation of MSC-derived DA cells. REST expression did not change during the induction process, thus we knocked down REST and subjected MSCs to the same neural induction cocktail. We observed increases in the protein level of the Na+ voltage-gated channel and tyrosine hydroxylase (TH). Electrophysiological analyses showed spontaneous firings and spontaneous postsynaptic currents, similar to native DA neurons. Taken together, these results show REST as the limiting gene in the generation of functional mature neurons from MSCs. (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:285 / 290
页数:6
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