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1.400038 重庆,陆军军医大学(第三军医大学)第一附属医院:神经内科
2.400038 重庆,陆军军医大学(第三军医大学)第一附属医院:神经外科
[李学刚,E-mail:67433433@qq.comLI Xuegang, E-mail:67433433@qq.com
收稿:2018-08-30,
修回:2018-11-20,
纸质出版:2019-03-15
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王必佳, 周振华, 陈康宁, 等. 自体荧光技术筛选恶性胶质瘤干细胞的优势分析[J]. 第三军医大学学报, 2019,41(5):437-441.
Bijia WANG, Zhenhua ZHOU, Kangning CHEN, et al. Analysis on advantages of autofluorescence technique in screening malignant of glioma stem cells[J]. Journal of Third Military Medical University, 2019, 41(5): 437-441.
王必佳, 周振华, 陈康宁, 等. 自体荧光技术筛选恶性胶质瘤干细胞的优势分析[J]. 第三军医大学学报, 2019,41(5):437-441. DOI: 10.16016/j.1000-5404.201808195.
Bijia WANG, Zhenhua ZHOU, Kangning CHEN, et al. Analysis on advantages of autofluorescence technique in screening malignant of glioma stem cells[J]. Journal of Third Military Medical University, 2019, 41(5): 437-441. DOI: 10.16016/j.1000-5404.201808195.
目的
2
探讨利用自体荧光技术筛选胶质瘤干细胞的效果。
方法
2
利用胶质瘤干细胞嗜核黄素的特点,在体外普通胶质瘤干细胞中加入核黄素培养,利用流式细胞仪筛选具有自发荧光的胶质瘤干细胞。CCK-8检测其体外增殖能力。建立小鼠模型,观察小鼠生存能力,观察肿瘤体积、质量。检测肿瘤组织Ki67、PCNA和Nestin的表达水平。
结果
2
通过流式细胞仪筛选出具有自发荧光的胶质瘤干细胞;CCK-8结果显示荧光胶质瘤干细胞的增殖能力更强(
P
<
0.01);体外荷瘤实验表明,荷有荧光干细胞的小鼠,其生存时间明显降低,肿瘤体积和质量明显增大(
P
<
0.01)。肿瘤石蜡切片免疫组化显示,载有荧光干细胞肿瘤切片中Ki67、PCNA和Nestin含量明显增高(
P
<
0.05)。荧光干细胞的增殖和恶性程度高于目前GL261肿瘤干细胞,同时也能筛选出部分CD133
-
的具有高恶性程度高和高侵袭性的胶质瘤干细胞。
结论
2
自体荧光技术能较好地筛选出恶性程度高的胶质瘤干细胞。
Objective
2
To determine the efficiency of autofluorescence technique in screening of glioma stem cells (GSCs).
Methods
2
Since GSCs favor riboflavin
the agent was added to the culture medium of normal glioma stem cells. Then flow cytometry was employed to screen glioma stem cells with autofluorescence. Subsequently
the proliferation of the obtained cells was detected by CCK-8 assay. Finally
a mouse model of xenograft was established to observe the survive and tumor size and weight. The expression of Ki67
PCNA and Nestin in the tumor mass was detected by immunohistochemical assay.
Results
2
Glioma stem cells with autofluorescence were successfully screened out by flow cytometry. CCK-8 assay indicated that the proliferation of autofluorescence glioma stem cells was significantly stronger (
P
<
0.01). In vitro tumor-bearing experiments suggested that mice with xenograft of fluorescent stem cells had significantly reduced survival time and increased tumor volume and weight (
P
<
0.01). Immunohistochemical assay showed that the expression levels of Ki67
PCNA and Nestin in the tumor mass were significantly increased (
P
<
0.05). The proliferation and malignancy of the autofluorescence GSCs were stronger than glioma stem GL261 cells screened by CD133
+
labeling. The CD133
-
GSCs with higher malignancy and invasion were also screened out with this method.
Conclusion
2
Autofluorescence technique can screen GSCs with high malignancy.
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