基础医学与临床 ›› 2025, Vol. 45 ›› Issue (1): 38-43.doi: 10.16352/j.issn.1001-6325.2025.01.0038

• 研究论文 • 上一篇    下一篇

姜黄素对嗜铬细胞瘤细胞系PC12增殖及侵袭的影响

张文倩1,2, 周玥2, 任卫东1,3*, 童安莉2*   

  1. 1.河北北方学院 研究生院,河北 张家口 075000;
    2.中国医学科学院 北京协和医学院 北京协和医院 内分泌科 国家卫生健康委员会内分泌重点实验室,北京 100730;
    3.河北北方学院附属第一医院 内分泌科,河北 张家口 075000
  • 收稿日期:2024-07-24 修回日期:2024-09-27 出版日期:2025-01-05 发布日期:2024-12-25
  • 通讯作者: *15530396532@126.com; tonganli@hotmail.com
  • 基金资助:
    国家重点研发计划(2021YFC2501600, 2021YFC2501603);中央高水平医院临床研究专项(2022-PUMCH-C-028);中国医学科学院医学与健康科技创新工程(2021-I2M-C&T-B-002,2021-I2M-1-007)

Effects of curcumin on the proliferation and invasiveness of pheochromocytoma cell line PC12

ZHANG Wenqian1,2, ZHOU Yue2, REN Weidong1,3*, TONG Anli2*   

  1. 1. Graduate School, Hebei North University, Zhangjiakou 075000;
    2. Departmentof Endocrinology, Key Laboratory of Endocrinology of National Health Commission, Peking Union Medical College Hospital, CAMS & PUMC, Beijing 100730;
    3. Department of Endocrinology, the First Hospital Affiliated to Hebei North University, Zhangjiakou 075000,China
  • Received:2024-07-24 Revised:2024-09-27 Online:2025-01-05 Published:2024-12-25
  • Contact: *15530396532@126.com; tonganli@hotmail.com

摘要: 目的 研究姜黄素对嗜铬细胞瘤细胞增殖、迁移、侵袭、凋亡的作用。方法 用不同浓度的姜黄素处理大鼠嗜铬细胞瘤 PC12细胞,采用CCK-8法检测细胞增殖,计算IC50;采用划痕实验检测细胞迁移能力,Transwell小室法检测细胞侵袭能力;采用流式细胞测量术检测细胞凋亡;qPCR检测细胞凋亡和抗凋亡基因(Bax和Bcl-2)的mRNA表达,Western blot检测Bax和Bcl-2蛋白表达。结果 姜黄素(10~80 μmol/L)呈浓度依赖性抑制 PC12细胞增殖,IC50为29 μmol/L。姜黄素呈浓度依赖性抑制PC12细胞迁移,对照组迁移率为66%,姜黄素10 μmol/L组、20 μmol/L组和30 μmol/L组迁移率分别为51%、5%和0.5%。姜黄素(20~30 μmol/L)能显著抑制PC12细胞侵袭(P<0.000 1)。此外,姜黄素显著促进PC12细胞凋亡,姜黄素10、20和30 μmol/L组凋亡细胞比对照组分别升高2.25%、18.53%和26.89%。姜黄素处理后,Bax基因mRNA和蛋白表达显著升高,Bcl-2基因mRNA和蛋白表达显著降低(P<0.05)。结论 姜黄素可显著抑制PC12细胞增殖、迁移、侵袭,促进细胞凋亡,其促凋亡作用可能与Bax和Bcl-2基因表达改变有关。

关键词: 姜黄素, PC12细胞, 凋亡, 侵袭, 迁移

Abstract: Objective To investigate the effects of curcumin on the proliferation, migration, invasion, and apoptosis of pheochromocytomacell line PC12. Methods PC12 cells were incubated with different concentrations of curcumin. Cell proliferation was assessed using the CCK-8 assay to determine the IC50. The scratch assay was used to evaluate cell migration and Transwell chambers were employed to assess cell invasiveness. Flow cytometry was used to analyze apoptosis. qPCR was conducted to measure the mRNA expression of pro-apoptotic (Bax) and anti- apoptotic (Bcl-2) genes, and Western blot was performed to detect Bax and Bcl-2 protein expressions. Results Curcumin(10-80 μmol/L) inhibited PC12 cell proliferation in a concentration-dependent manner, with an IC50 as 29 μmol/L. Curcumin also suppressed PC12 cell migration in a concentration-dependent mode; the migration rate decreased from 66% in the control group down to 51%, 5%, and 0.5% in the 10, 20, and 30 μmol/L curcumin groups, respectively. Curcumin at concentrations of 20-30 μmol/L significantly reduced PC12 cell invasiveness(P<0.000 1). Moreover, curcumin significantly promoted PC12 cell apoptosis; the percentage of apoptotic cells increased by 2.25%, 18.53%, and 26.89% in the 10, 20, and 30 μmol/L curcumin groups as compared to those of control group, respectively. Curcumin treatment resulted in a significant up-regulation of Bax mRNA and protein expression, and a significant down-regulation of Bcl-2 mRNA and protein expression(P<0.05). Conclusions Curcumin may significantly inhibit the proliferation, migration, and invasion of PC12 cells and arouse cell apoptosis. Its pro-apoptotic effect may be associated with alterations in the expression of Bax and Bcl-2 genes.

Key words: curcumin, PC12 cell, apoptosis, invasion, migration

中图分类号: