Applied Science Department, Indian Institute of Information Technology, Allahabad, UP, India.
J Mol Neurosci. 2021 May;71(5):889-901. doi: 10.1007/s12031-020-01714-5. Epub 2020 Oct 13.
Neurodegenerative disorders have become the leading cause of chronic pain and death. Treatments available are not sufficient to help the patients as they only alleviate the symptoms and not the cause. In this regard, stem cells therapy has emerged as an upcoming option for the replacement of dead and damaged neurons. Stem cells, in general, are characterized as cells exhibiting potency properties, i.e., on being subjected to specific conditions they transform into cells of another lineage. Of all the types, mesenchymal stem cells (MSCs) are known for their pluripotent nature without the obstacle of ethical concern surrounding the procurement of other cell types. Although fibroblasts are quite similar to MSCs morphologically, certain markers like CD73, CD 90 are specific to MSCs, making both the cell types distinguishable from each other. This is implemented while procuring MSCs from a plethora of sources like umbilical cord blood, adipose tissue, bone marrow, etc. Among these, bone marrow MSCs are the most widely used type for neural regeneration. Neural regeneration is achieved via transdifferentiation. Several studies have either transplanted the stem cells into rodent models or have carried out transdifferentiation in vitro. The process involves a combination of growth factors, pre-treatment factors, and neuronal differentiation inducing mediums. The results obtained are characterized by neuron-like morphology, expression of markers, along with electrophysical activity in some. Recent attempts involve exploring biomaterials that may mimic the native ECM and therefore can be directly introduced at the site of interest. The review gives a brief description of MSCs, their sources and markers, and the different attempts that have been made towards achieving the goal of differentiating MSCs into neurons.
神经退行性疾病已成为慢性疼痛和死亡的主要原因。现有的治疗方法不足以帮助患者,因为它们只能缓解症状,而不能治疗病因。在这方面,干细胞疗法已成为替代死亡和受损神经元的一种新兴选择。干细胞通常具有多能性特征,即受到特定条件的影响,它们会转化为另一种谱系的细胞。在所有类型中,间充质干细胞(MSCs)因其多能性而闻名,而且不存在围绕获取其他细胞类型的伦理问题的障碍。尽管成纤维细胞在形态上与 MSCs 非常相似,但某些标记物,如 CD73、CD90,是 MSCs 特有的,这使得两种细胞类型能够相互区分。这是在从脐带血、脂肪组织、骨髓等多种来源中获取 MSCs 时实现的。其中,骨髓间充质干细胞是最常用于神经再生的类型。神经再生是通过转分化实现的。有几项研究将干细胞移植到啮齿动物模型中,或在体外进行转分化。该过程涉及生长因子、预处理因子和神经元分化诱导培养基的组合。获得的结果具有神经元样形态、标志物表达以及在某些情况下具有电生理活性的特点。最近的尝试涉及探索可能模拟天然细胞外基质的生物材料,因此可以直接引入感兴趣的部位。该综述简要描述了 MSCs、它们的来源和标记物,以及为实现将 MSCs 分化为神经元的目标而进行的不同尝试。