Fu Xiao-Rui, Sun Zhen-Chang, Zhang Ming-Zhi
Department of Oncology, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.
Zhong Yao Cai. 2012 Mar;35(3):433-8.
To investigate the effects of extract from Prunella vulgaris on proliferation of human B lymphoma cell line Raji cells anf T lymphoma cell line Jurkat cells and discuss the mechanism.
Used different concentrations of extract from Prunella vulgaris to treat Raji and Jurkat cells and collected cells after 48 h respectively, the proliferation inhibition rate, the DNA Ladder and the apoptosis rate of Raji and Jurkat cells were examined by MTT assay, agarose gel electrophoresis and flow cytometry respectively; Western blot was used to detect the change of BCL-2, BAX protein.
Different concentrations of the extract from Prunella vulgaris could inhibit the proliferation of both Raji and Jurkat cells remarkably (P < 0.01), the IC50 of Raji cells, 18.01 +/- 0.92 microg/mL, was lower than that of Jurkat, the difference was significant statistically (P < 0.05); Apoptosis related DNA Ladder appeared after treated Raji and Jurkat cells with the extract from Prunella vulgaris; Compared with the control group, with the increase of the concentration of the extract from Prunella vulgaris, the early cell apoptosis rate of Raji and Jurkat were all increased,the early cell apoptosis rate of the extract from Prunella vulgaris of 15, 20 and 25 microg/mL treated Raji and Jurkat cells were (9.46 +/- 0.25)%, (21.68 +/- 0.46)%, (35.03 +/- 0.35)% and (4.06 +/- 0.14)%, (13.59 +/- 0.23)%, (22.92 +/- 0.20)% respectively. With the same concentration, the early apoptosis rate of Raji cells was higher than that of Jurkat cells significantly (P < 0.01); Compared with the control group, with the in- crease of the concentration of the extract from Prunella vulgaris, the expression of BCL-2 protein was down-regulated and BAX up-regulated, With the same concentration, the decline degree of BCL-2 protein expression and the increase degree of BAX protein expression in Raji cells was more remarkable than that in Jurkat cells, the difference was significant (P < 0.05).
The extract from Prunella vulgaris can inhibit the proliferation of lymphoma cells and the inhibition is realized by inducing apoptosis, the mechanism of inducing cell apoptosis with extract from Prunella vulgaris is probably related with the BAX and BCL-2 protein expression, the inhibition effect on Raji cells is greater than that of Jurkat cells.
探讨夏枯草提取物对人B淋巴瘤细胞系Raji细胞和T淋巴瘤细胞系Jurkat细胞增殖的影响并探讨其机制。
用不同浓度的夏枯草提取物分别处理Raji细胞和Jurkat细胞,48 h后收集细胞,分别采用MTT法、琼脂糖凝胶电泳法及流式细胞术检测Raji细胞和Jurkat细胞的增殖抑制率、DNA Ladder及凋亡率;采用Western blot法检测BCL-2、BAX蛋白的变化。
不同浓度的夏枯草提取物均能显著抑制Raji细胞和Jurkat细胞的增殖(P<0.01),Raji细胞的IC50为18.01±0.92 μg/mL,低于Jurkat细胞,差异有统计学意义(P<0.05);夏枯草提取物处理Raji细胞和Jurkat细胞后出现凋亡相关的DNA Ladder;与对照组比较,随着夏枯草提取物浓度的增加,Raji细胞和Jurkat细胞的早期细胞凋亡率均升高,夏枯草提取物15、20、25 μg/mL处理Raji细胞和Jurkat细胞的早期细胞凋亡率分别为(9.46±0.25)%、(21.68±0.46)%、(35.03±0.35)%和(4.06±0.14)%、(13.59±0.23)%、(22.92±0.20)%。相同浓度时,Raji细胞的早期凋亡率显著高于Jurkat细胞(P<0.01);与对照组比较,随着夏枯草提取物浓度的增加,BCL-2蛋白表达下调,BAX蛋白表达上调,相同浓度时,Raji细胞BCL-2蛋白表达下降程度及BAX蛋白表达增加程度均较Jurkat细胞更显著,差异有统计学意义(P<0.05)。
夏枯草提取物能抑制淋巴瘤细胞增殖,其抑制作用是通过诱导凋亡实现的,夏枯草提取物诱导细胞凋亡的机制可能与BAX、BCL-2蛋白表达有关,对Raji细胞的抑制作用大于Jurkat细胞。