陈朋
,刘睿
,骆翔
,喻志源
,王伟
,陈雪.小胶质细胞培养上清液对鼻咽癌细胞迁移和侵袭能力的影响[J].神经损伤功能重建,2020,15(3):125-128 |
小胶质细胞培养上清液对鼻咽癌细胞迁移和侵袭能力的影响 |
Effect of Microglia Cell Supernatant on Migration and Invasion of Nasopharyngeal CarcinomaCells |
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DOI: |
中文关键词: 人小胶质细胞 鼻咽癌细胞 迁移 侵袭 |
英文关键词: microglia nasopharyngeal carcinoma migration invasion |
基金项目:国家自然科学基
金(No.81771341);
湖北省自然科学
基金(No.2017CFB
705) |
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中文摘要: |
目的:研究未活化和活化态人小胶质细胞系CHME-5培养上清液对鼻咽癌细胞CNE-2迁移、侵袭能
力的影响。方法:采用1 μg/mL LPS活化人小胶质细胞系CHME-5,收集未活化和LPS活化的CHME-5培养
上清液。分为对照组(无血清培养基)、45%上清组、90%上清组、LPS组(LPS干预的小胶质细胞上清)、45%
LPS上清组、90%LPS上清组。使用划痕实验和Transwell小室建立鼻咽癌细胞CNE-2的迁移模型,观察不
同浓度的未活化/活化小胶质细胞培养上清液对鼻咽癌细胞迁移能力的影响;使用Transwell小室建立鼻咽
癌细胞CNE-2的侵袭模型,用结晶紫染色观察不同浓度的未活化/活化小胶质细胞培养上清液对鼻咽癌细
胞侵袭能力的影响。结果:低浓度(45%)和高浓度(90%)未活化/活化的小胶质细胞培养上清液均促进鼻咽
癌细胞迁移和侵袭。结论:无论小胶质细胞是否活化,其培养上清液均促进鼻咽癌细胞的迁移和侵袭。 |
英文摘要: |
To study the effect of unactivated/activated human microglia cell line CHME-5 on the
migration and invasion of nasopharyngeal carcinoma cell line CNE-2. Methods: Human microglia cell line
CHME-5 was cultured, and 1 μg/mL LPS was used to activate cells. Unactivated/activated cell supernatant was
collected. For the experiment, we established 6 groups: control group, 45% supernatant group, 90% supernatant
group, LPS group (LPS activated microglia supernatant), 45% LPS supernatant group, and 90% LPS supernatant
group. The wound healing assay and Transwell inserts were used to establish the nasopharyngeal carcinoma cell
line CNE-2 migration model, and the effect of unactivated/activated microglia supernatant on the migration of
the cell was observed. Transwell inserts were used to establish the nasopharyngeal carcinoma cell line CNE-2 invasion model, and crystal violet staining was used to observe the effect of microglia supernatant on the migration
of the cell. Results: Low (45%) and high (90%) concentrations of unactivated/activated microglia supernatant
promoted the migration and invasion of nasopharyngeal cancer cells. Conclusion: Both unactivated and activated microglia supernatant promote the migration and invasion of nasopharyngeal carcinoma cells. |
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