Department of Surgery and Translational Medicine, University of Milano-Bicocca, 20900 Monza, Italy.
Department of Biomedical, Surgical and Dental Sciences, University of Milan, 20129 Milano, Italy ; IRCCS Galeazzi Orthopaedic Institute, 20161 Milano, Italy.
J Immunol Res. 2014;2014:987678. doi: 10.1155/2014/987678. Epub 2014 Mar 5.
The spontaneous expression of neural markers, already demonstrated in bone marrow (BM) mesenchymal stem cells (MSCs), has been considered as evidence of the MSCs' predisposition to differentiate toward neural lineages, supporting their use in stem cell-based therapy for neural repair. In this study we have evaluated, by immunocytochemistry, immunoblotting, and flow cytometry experiments, the expression of neural markers in undifferentiated MSCs from different sources: human adipose stem cells (hASCs), human skin-derived mesenchymal stem cells (hS-MSCs), human periodontal ligament stem cells (hPDLSCs,) and human dental pulp stem cells (hDPSCs). Our results demonstrate that the neuronal markers β III-tubulin and NeuN, unlike other evaluated markers, are spontaneously expressed by a very high percentage of undifferentiated hASCs, hS-MSCs, hPDLSCs, and hDPSCs. Conversely, the neural progenitor marker nestin is expressed only by a high percentage of undifferentiated hPDLSCs and hDPSCs. Our results suggest that the expression of β III-tubulin and NeuN could be a common feature of stem cells and not exclusive to neuronal cells. This could result in a reassessment of the use of β III-tubulin and NeuN as the only evidence proving neuronal differentiation. Further studies will be necessary to elucidate the relevance of the spontaneous expression of these markers in stem cells.
骨髓(BM)间充质干细胞(MSCs)中已证实的神经标志物的自发表达被认为是 MSCs 向神经谱系分化的倾向性的证据,支持将其用于基于干细胞的神经修复治疗。在这项研究中,我们通过免疫细胞化学、免疫印迹和流式细胞术实验评估了来自不同来源的未分化 MSCs 中神经标志物的表达:人脂肪干细胞(hASCs)、人皮肤衍生的间充质干细胞(hS-MSCs)、人牙周膜干细胞(hPDLSCs)和人牙髓干细胞(hDPSCs)。我们的结果表明,神经元标志物 β III-微管蛋白和 NeuN 与其他评估的标志物不同,自发表达于非常高比例的未分化 hASCs、hS-MSCs、hPDLSCs 和 hDPSCs。相反,神经祖细胞标志物巢蛋白仅由高比例的未分化 hPDLSCs 和 hDPSCs 表达。我们的结果表明,β III-微管蛋白和 NeuN 的表达可能是干细胞的共同特征,而不仅仅是神经元细胞所特有的。这可能导致重新评估仅使用β III-微管蛋白和 NeuN 作为证明神经元分化的唯一证据。需要进一步的研究来阐明这些标记物在干细胞中自发表达的相关性。