Liqing Yang, Jia Geng, Jiqing Cao, Ran Gu, Fei Chen, Jie Kong, Yanyun Wang, Cheng Zhang
Department of Neurology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China.
Neuroreport. 2011 Jun 11;22(8):370-3. doi: 10.1097/WNR.0b013e3283469615.
The capacity of human adipose-derived stem cells (hADSCs) to differentiate into motor neurons and the identity of molecular factors that confer hADSCs with the competence of motor neurons have yet to be elucidated. Here, retinoic acid and sonic hedgehog were applied to examine whether hADSCs could be differentiated into motor neurons. As early as 6 h after induction, hADSCs were changed toward neuronal morphology. After induction, hADSCs showed positive immunocytochemical staining for β-III-tubulin, choline acetyltransferase, and neuron-specific enolase. Reverse-transcriptase polymerase chain reaction characterization indicated that cells differentiated from hADSCs were restricted to the ventral spinal fate (Nkx2.2, Pax6, Hb9, and Olig2). Our results suggest that hADSCs may be a potential candidate in cellular therapy for motor neuron disease.
人脂肪来源干细胞(hADSCs)分化为运动神经元的能力以及赋予hADSCs运动神经元能力的分子因子的特性尚未阐明。在此,应用视黄酸和音猬因子来检测hADSCs是否可分化为运动神经元。早在诱导后6小时,hADSCs就向神经元形态转变。诱导后,hADSCs对β-III-微管蛋白、胆碱乙酰转移酶和神经元特异性烯醇化酶呈免疫细胞化学染色阳性。逆转录聚合酶链反应特征表明,从hADSCs分化而来的细胞局限于腹侧脊髓命运(Nkx2.2、Pax6、Hb9和Olig2)。我们的结果表明,hADSCs可能是运动神经元疾病细胞治疗的潜在候选者。