胆管癌体外嗜神经生长的实验研究。

JRSM short reports Pub Date : 2013-09-13 eCollection Date: 2013-01-01 DOI:10.1177/2042533313476690
Yu-Xue Wang, Wei Liu, Xin-Yu Tan, Hui-Huan Tang
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引用次数: 0

摘要

目的:胆管癌的神经周围侵犯发生在疾病的早期,但往往要到晚期才被发现。迫切需要研究胆管癌侵袭神经周围的行为和机制,以建立一个有用的新模型。这项工作的目的是建立一个新的模型来解决这个问题。设计:神经细胞和胆管癌细胞共培养,模拟胆管癌的嗜神经性侵袭。实验环境:用神经胶质细胞源性神经营养因子和维甲酸诱导人胚胎干细胞形成神经细胞;神经细胞与胆管癌细胞在Transwell室共培养。实验对象:采用人胚胎干细胞和胆管癌细胞。主要观察指标:采用配对t检验比较共培养组与对照组穿透性胆管癌细胞计数。结果:诱导后24 h和48 h分别观察到神经球和神经样细胞的形成;孵育96 h后,突触从神经样细胞体中突出。孵育48 h后,细胞免疫细胞化学染色显示神经元样细胞和胶质细胞样细胞中分别表达突触素和胶质原纤维酸性蛋白。共培养组通过基质/聚对苯二甲酸乙二醇酯膜从Transwell的上腔渗透到下腔的胆管癌细胞数量明显多于对照组(68±8.3个/场比46±5.7个/场,P < 0.05)。结论:该模型是研究胆管癌神经周浸润的有效工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

In vitro neuraotropic growth of cholangiocarcinoma: an experimental study.

In vitro neuraotropic growth of cholangiocarcinoma: an experimental study.

In vitro neuraotropic growth of cholangiocarcinoma: an experimental study.

In vitro neuraotropic growth of cholangiocarcinoma: an experimental study.

Objective: Perineural invasion of cholangiocarcinoma happens in the early stage of the disease but is often not recognized until its later stages. Research about the behaviour and mechanism of perineural invasion by cholangiocarcinoma is urgently needed for a useful new model. The aim of this work is to establish a novel model to address the problem.

Design: Neural cells and cholangiocarcinoma cells were co-cultured to mimic the neurotropic invasion of cholangiocarcinoma.

Setting: Human embryonic stem cells were induced to form neural cells by glial cell-derived neurotropic factor and retinoic acid; neural cells and cholangiocarcinoma cells were co-cultured in Transwell chamber.

Participants: Human embryonic stem cells and cholangiocarcinoma cells were applied.

Main outcome measures: Paired t-test was used to compare the counts of penetrating cholangiocarcinoma cells in co-culture and control group.

Results: Formation of neurospheres and neural-like cells were observed following induction at 24 and 48 h, respectively; synapses were viewed to protrude from neural-like cell bodies after incubation for 96 h. Forty-eight hours after incubation, immunocytochemical staining of the cells showed that synaptophysin and glial fibrillary acidic protein were expressed in the neuron-like cells and gliocytes-like cells, respectively. The cholangiocarcinoma cells that had penetrated through the Matrigel/polyethylene terephthalate membrane from the upper chamber to the lower chamber of the Transwell in the co-culture group were significantly more numerous than those in the control group (68 ± 8.3/field versus 46 ± 5.7/field, P < 0.05).

Conclusion: The novel model is a valuable tool to study the perineural invasion of cholangiocarcinoma.

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