[Culture, purification and biological characters of olfactory ensheathing cells from adult transgenic mice].

Shi yan sheng wu xue bao Pub Date : 2005-08-01
Chun Ting Wang, Shi Hua He, Hao Yang, Ping Zhang, Ling Ling Fei, Si Wei You, Gong Ju
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Abstract

Several studies have demonstrated the potential of olfactory ensheathing cells (OECs) for the repair of central and peripheral nerve injury. In this work, ensheathing cells that express the receptor gene coding for enhanced green fluorescent protein (eGFP) from adult mice were isolated and purified, and then, its biological characters were examined in vitro. The work was based on combinations of fluorescence confocal, phase contrast, cell proliferation assay and immunolabeling identification. The results showed that (1) two major morphologically and immunohistochemically distinct types of cells were present after 15 days in the primary cultures of adult transgenic mice olfactory nerves and glomerular layers of the olfactory bulb. One cell type was bipolar or multipolar OECs and strained positively for P75 low affinity neurotrophic receptor (P75N), S100, and glial fibrillary acidic protein(GFAP). The other type was fibroblasts with flat or endothelial-like shape, and reacted with antibody against Thy1.1. (2) A simple, inexpensive method for purifying ensheathing cells, in which various harvested cell types showed different rates of attachment to the uncoated culture ware, was developed. This technique neither binds any antibodies nor requires any costly equipment, and yields a large number of highly purified cells. (3) In sequential observations over 22 days in culture, the population of purified cells was maintained and continued to proliferate for longer. This experiment not only supported and advanced the ensheathing cell research but also offered ideal materials of in vivo transplantation for the repair of CNS injury.

[成年转基因小鼠嗅鞘细胞的培养、纯化及生物学特性研究]。
一些研究已经证明了嗅鞘细胞(OECs)在中枢和周围神经损伤修复中的潜力。本文从成年小鼠中分离纯化了表达增强绿色荧光蛋白(eGFP)受体基因的鞘细胞,并对其体外生物学特性进行了研究。这项工作是基于荧光共聚焦、相衬、细胞增殖试验和免疫标记鉴定的组合。结果表明:(1)转基因成年小鼠嗅神经和嗅球肾小球原代培养15天后,在形态学和免疫组织化学上存在两种主要的细胞类型。一种细胞类型为双极或多极OECs, P75低亲和力神经营养受体(P75N)、S100和胶质原纤维酸性蛋白(GFAP)阳性。另一类是扁平或内皮样形状的成纤维细胞,与抗Thy1.1抗体反应。(2)开发了一种简单、廉价的纯化鞘细胞的方法,在这种方法中,各种收获的细胞类型对未包被的培养器皿的附着率不同。这种技术既不结合任何抗体,也不需要任何昂贵的设备,而且可以产生大量高度纯化的细胞。(3)在22天的连续培养观察中,纯化细胞的群体得以维持并持续增殖更长时间。该实验不仅支持和推进了鞘细胞的研究,而且为中枢神经系统损伤的修复提供了理想的体内移植材料。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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