嗅粘膜来源的间充质干细胞向许旺细胞样表型分化,为周围神经再生提供来源

Katelyn Neuman, Abigail N Koppes, Ryan A Koppes
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摘要

间充质干细胞(MSCs)是治疗周围神经损伤的一种前景广阔的干细胞来源。在这里,我们首次研究了嗅粘膜间充质干细胞(OM-MSC)向许旺细胞(SC)样表型的分化。嗅粘膜间充质干细胞是用于周围神经修复的潜在施旺细胞的有利来源,因为与自体神经采集和分离相比,它可以通过微创手术完成分离。在这里,将许旺细胞条件培养基(SCCM)或确定的生长因子补充培养基(GF)应用于 OM-MSC 21 天。通过免疫细胞化学和 RT-qPCR 鉴定了分化过程和所产生的细胞群。在体外共培养模型中对分化群体的功能进行了评估,以评估与并列于原生间充质干细胞的感觉神经元(背根神经节)之间的相互作用。与未分化的间充质干细胞相比,使用 SCCM 和 GF 培养基的分化方案导致了形态、基因表达和功能的显著变化,代表了间充质干细胞的关键特征。具体来说,在共培养模型中,分化后的种群表现出拉长的纺锤形形态、高度偏心、S-100、CD44 和 NGF 表达增加以及髓鞘碱性蛋白与神经元共定位。总之,这项工作凸显了 OM 间充质干细胞扩增和分化为 SCs 的潜力,从而改善合成支架或用于脱细胞异体移植的神经修复。
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Olfactory Mucosa-Derived Mesenchymal Stem Cells Differentiate Towards a Schwann Cell-Like Phenotype Towards Sourcing for Peripheral Nerve Regeneration
Mesenchymal stem cells (MSCs) are a promising source of stem cells for treating peripheral nerve injuries. Here, we present the first investigation of differentiation of olfactory mucosa-derived MSC (OM-MSC) towards a Schwann Cell (SC)-like phenotype. OM-MSCs are an advantageous potential source of SCs for peripheral nerve repair, as isolation can be accomplished with a minimally invasive procedure compared to autologous nerve harvest and isolation. Here, Schwann Cell Conditioned Media (SCCM) or a defined growth factor supplemented media (GF) was applied to OM-MSC for twenty-one days. The differentiation process and resulting populations were characterized by immunocytochemistry and RT-qPCR. Functionality of differentiated populations was assessed in an in vitro co-culture model to evaluate interaction with sensory neurons (dorsal root ganglia) juxtaposed to native SCs. Compared to undifferentiated MSCs, differentiation protocols resulted in significant changes in morphology, gene expression, and functionality using SCCM and GF media, representing key characteristics of SCs. Specifically, differentiated populations exhibit elongated, spindle-like morphologies, a high degree of eccentricity, increased S-100, CD44, and NGF expression, and colocalization of myelin basic proteins with neurites in the co-culture model. In conclusion, this work highlights the potential of OM-MSCs to be expanded and differentiated to SCs to improve synthetic scaffolds or for use in decellularized allografts for nerve repair.
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