{"title":"Potential sources of stem cells as a regenerative therapy for Parkinson's disease.","authors":"Abir Oueida El-Sadik","doi":"10.2147/SCCAA.S14626","DOIUrl":null,"url":null,"abstract":"<p><p>Stem cells are believed to hold enormous promise as potential replacement therapy in the treatment of neurodegenerative diseases such as Parkinson's disease (PD). Stem cells were investigated to be the alternative therapeutic source capable of differentiating into dopamine (DA) neurons. Multiple important signaling factors were recorded for the induction of DA neuronal traits from mouse embryonic stem cells (ESCs) such as fibroblast growth factor 8, sonic hedgehog, and Wnt 1. Recent protocols were described for the differentiation of human ESCs into DA neurons, achieving high efficiency of DA neuronal derivation. Despite that, the use of human ESCs is still ethically controversial. The transcription factors necessary for DA neuron development from adult neural stem cells (NSCs), such as Pitx3, Nurr1, En-1, En-2, Lmx1a, Lmx1b, Msx1, and Ngn2, were investigated. In addition to replacement of lost DA neurons, adult NSCs were recorded to provide neuroprotective and neurogenic factors for the mesencephalon. In addition, induced pluripotent stem cells and bone marrow-derived mesenchymal stem cells represent reliable stem cell sources of DA neurons. Future studies are recommended to provide further insight into the regenerative capacity of stem cells needed for the treatment of PD. </p>","PeriodicalId":44934,"journal":{"name":"Stem Cells and Cloning-Advances and Applications","volume":"3 ","pages":"183-91"},"PeriodicalIF":1.7000,"publicationDate":"2010-12-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781753/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Stem Cells and Cloning-Advances and Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2147/SCCAA.S14626","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Stem cells are believed to hold enormous promise as potential replacement therapy in the treatment of neurodegenerative diseases such as Parkinson's disease (PD). Stem cells were investigated to be the alternative therapeutic source capable of differentiating into dopamine (DA) neurons. Multiple important signaling factors were recorded for the induction of DA neuronal traits from mouse embryonic stem cells (ESCs) such as fibroblast growth factor 8, sonic hedgehog, and Wnt 1. Recent protocols were described for the differentiation of human ESCs into DA neurons, achieving high efficiency of DA neuronal derivation. Despite that, the use of human ESCs is still ethically controversial. The transcription factors necessary for DA neuron development from adult neural stem cells (NSCs), such as Pitx3, Nurr1, En-1, En-2, Lmx1a, Lmx1b, Msx1, and Ngn2, were investigated. In addition to replacement of lost DA neurons, adult NSCs were recorded to provide neuroprotective and neurogenic factors for the mesencephalon. In addition, induced pluripotent stem cells and bone marrow-derived mesenchymal stem cells represent reliable stem cell sources of DA neurons. Future studies are recommended to provide further insight into the regenerative capacity of stem cells needed for the treatment of PD.
干细胞被认为是治疗帕金森病(PD)等神经退行性疾病的潜在替代疗法,前景广阔。研究发现,干细胞是能够分化成多巴胺(DA)神经元的替代疗法来源。研究记录了多种重要的信号因子,如成纤维细胞生长因子8、声波刺猬和Wnt 1,可诱导小鼠胚胎干细胞(ESCs)分化成多巴胺(DA)神经元。最近,有人描述了将人类胚胎干细胞分化成 DA 神经元的方案,实现了 DA 神经元的高效衍生。尽管如此,使用人类 ESCs 在伦理上仍存在争议。研究人员研究了成体神经干细胞(NSCs)发育DA神经元所需的转录因子,如Pitx3、Nurr1、En-1、En-2、Lmx1a、Lmx1b、Msx1和Ngn2。除了替代失去的 DA 神经元,记录的成体 NSCs 还能为间脑提供神经保护和神经源因子。此外,诱导多能干细胞和骨髓间充质干细胞是DA神经元的可靠干细胞来源。建议今后开展研究,进一步了解治疗帕金森病所需的干细胞再生能力。