Zhang Xuefeng, Ren Zuyuan, Zuo Jin, Su Changbao, Wang Renzhi, Chang Yongsheng, Fang Fude
Neurosurgery Department, Peking Union Medical College Hospital, CAMS & PUMC, Beijing 100730.
Chin Med Sci J. 2002 Mar;17(1):22-6.
To illuminate the regulating effect of all-trans retinoic acid (ATRA) on gap junctional intercellular communication (GJIC) and connexin 43 (Cx43) gene expression in glioma cells, which is tissue- and organ-specific.
Rat C6 glioma cells were exposed to ATRA at a concentration of 1, 10, 100 micromol/L and the GJIC function of the cells was examined with scrape-loading dye transfer assay 24 hours, 48 hours and 72 hours after ATRA treatment. The effect of ATRA on Cx43 gene expression was measured with semiquantitative reverse transcription polymerase chain reaction (RT-PCR) 24 hours after ATRA exposure.
The GJIC function of C6 glioma cells was significantly increased by ATRA at each concentration applied. The dye passed 4 to 5 rows of cells from the scraping edge in ATRA treated cells, but only 1 or 2 rows in the control. The augment effect was observed 24 hours after each concentration ATRA treatment, and lasted till 72 hours after treatment with 1 micromol/L and 10 micromol/L ATRA. Forty-eight hours after exposed to 100 micromol/L ATRA, the enhancement of GJIC was less obvious. There was no significant increase induced by ATRA on the transcription of Cx43 gene, as demonstrated by semiquantitative RT-PCR.
ATRA turned out to be a potent enhancer on GJIC function in C6 glioma cells, andthe enhancement effect was most probable at post-transcriptional level.
阐明全反式维甲酸(ATRA)对胶质瘤细胞间隙连接细胞间通讯(GJIC)及连接蛋白43(Cx43)基因表达的调节作用,该调节作用具有组织和器官特异性。
将大鼠C6胶质瘤细胞分别暴露于浓度为1、10、100 μmol/L的ATRA中,在ATRA处理后24小时、48小时和72小时,采用刮伤-加载染料转移试验检测细胞的GJIC功能。在ATRA处理24小时后,用半定量逆转录聚合酶链反应(RT-PCR)检测ATRA对Cx43基因表达的影响。
在所应用的各浓度ATRA作用下,C6胶质瘤细胞的GJIC功能均显著增强。在经ATRA处理的细胞中,染料从刮伤边缘穿过4至5排细胞,而在对照细胞中仅穿过1或2排。在各浓度ATRA处理后24小时观察到增强作用,在用1 μmol/L和10 μmol/L ATRA处理后持续至72小时。在暴露于100 μmol/L ATRA 48小时后,GJIC的增强作用不太明显。半定量RT-PCR结果表明,ATRA对Cx43基因转录无显著增加作用。
ATRA是C6胶质瘤细胞GJIC功能的有效增强剂,其增强作用最可能发生在转录后水平。