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首页> 外文期刊>Cell transplantation >Toward defining the regenerative potential of olfactory mucosa: Establishment of schwann cell-free adult canine olfactory ensheathing cell preparations suitable for transplantation
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Toward defining the regenerative potential of olfactory mucosa: Establishment of schwann cell-free adult canine olfactory ensheathing cell preparations suitable for transplantation

机译:定义嗅觉粘膜的再生潜力:建立适合移植的无施万恩细胞的成年犬嗅鞘细胞制剂

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摘要

Olfactory mucosa (OM)-derived olfactory ensheathing cells (OECs) are attractive candidates for autologous cell transplantation-based therapy of nervous system injury. However, defining the regenerative capacity of OM-derived OECs is impeded by the fact that cell cultures used for transplantation may contain significant amounts of contaminating trigeminal nerve Schwann cells that escape identification by sharing in vitro expression of OEC markers. The aim of the present study, therefore, was to quantify contaminating Schwann cells in OEC preparations and to develop a protocol for their specific depletion. Based on the observation that freshly dissociated, but not cultured, OECs and Schwann cells display differential expression of HNK-1 and p75NTR, magnet-activated cell sorting (MACS) was used to deplete myelinating (HNK-1-positive) and nonmyelinating (p75NTR-positive) Schwann cells from primary cell suspensions containing HNK-1-/p75NTR-negative OECs. Upregulation of p75NTR expression in OECs during culturing allowed their subsequent MACS-based separation from fibroblasts. Immunofluorescence analysis of freshly dissociated OM prior to MACS depletion revealed that 21% of the total and 56% of all CNPase-positive cells, representing both OECs and Schwann cells, expressed the Schwann cell antigens HNK-1 or p75NTR, indicating that freshly dissociated OM prior to culturing contained as many Schwann cells as OECs, while olfactory bulb (OB) primary cell suspensions revealed lower levels of Schwann cell contamination. Interestingly, neurite growth of neonatal rat dorsal root ganglion (DRG) neurons cocultured with OM-OECs, OB-OECs, and fibular nerve (FN) Schwann cells used as control was significantly higher in the presence of OECs than of Schwann cells. The first report on identification and specific depletion of Schwann cells from OEC preparations provides a solid basis for future efforts to fully define the regenerative potential of nasal mucosa OECs. ? 2013 Cognizant Comm. Corp.
机译:嗅觉粘膜(OM)衍生的嗅鞘细胞(OEC)是基于自体细胞移植的神经系统损伤治疗的诱人候选物。但是,由于用于移植的细胞培养物中可能含有大量的污染性三叉神经雪旺细胞,而这些细胞通过共享OEC标记物的体外表达而逃避了鉴定,因此,无法定义OM衍生的OEC的再生能力。因此,本研究的目的是量化OEC制剂中污染的雪旺氏细胞,并开​​发一种针对其特定消耗的方案。基于观察到的是OEC和Schwann细胞在新鲜分离但未培养的情况下表现出HNK-1和p75NTR的差异表达,因此采用磁激活细胞分选(MACS)来消除髓鞘形成(HNK-1阳性)和非髓鞘形成(p75NTR阳性)来自含有HNK-1- / p75NTR阴性OEC的原代细胞悬液的雪旺氏细胞。在培养期间OEC中p75NTR表达的上调允许其随后基于MACS从成纤维细胞中分离出来。在MACS耗尽之前对新鲜离解的OM进行的免疫荧光分析表明,代表OEC和Schwann细胞的CNPase阳性细胞总数的21%和所有CNPase阳性细胞的56%表达了施旺细胞抗原HNK-1或p75NTR,这表明新鲜离解的OM培养前所含的雪旺氏细胞与OEC一样多,而嗅球(OB)的原代细胞悬浮液显示出较低水平的雪旺氏细胞污染。有趣的是,在存在OEC的情况下,与OM-OEC,OB-OEC和腓骨神经(FN)Schwann细胞共培养的新生大鼠背根神经节(DRG)神经元的神经突生长明显高于Schwann细胞。关于从OEC制剂中鉴定和特定清除雪旺细胞的第一份报告为未来努力充分确定鼻粘膜OEC的再生潜力提供了坚实的基础。 ? 2013 Cognizant Comm。公司

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