Chen Nan, Zhang Jie, Xu Min, Wang Ting, Wang Yu-ling, Pei Ying-hua
Department of Pulmonary Medicine, Beijing TianTan Hospital, Capital Medical University, Beijing 100050, China.
Department of Pulmonary Medicine, Beijing TianTan Hospital, Capital Medical University, Beijing 100050, China. Email:
Zhonghua Jie He He Hu Xi Za Zhi. 2013 Sep;36(9):655-60.
To observe the inhibitory effect and potential mechanism of mitomycin C and paclitaxel on the proliferation of Human Pulmonary Fibroblast in vitro. So as to providing an experimental reference for the design of drug eluting airway stents.
Cell viability was measured by MTT assay after different concentrations of mitomycin C or paclitaxel varying from 10(-1)1 mol/L to 10(-4) mol/L had been applied to the fibroblasts for 24, 48 or 72 h, respectively. Cell apoptosis was assessed by flow cytometry using dual staining with annexin V-FITC and propidium iodide 48 h after administering mitomycin C or paclitaxel at a concentration of 5×10(-6), 10(-5), 5×10(-5), 10(-4), 2×10(-4) mol/L, respectively. And the morphological character of cell apoptosis was observed by Hoechst 33342 fluorescent staining.
The results of MTT revealed that cell proliferation were inhibited by mitomycin C and paclitaxel at all concentrations and exposure times. Among them, the inhibitory effect of mitomycin C were weak when the concentrations were between 10(-1)1 mol/L to 10(-8) mol/L. And within this context, the inhibitory ratio didn't correspond to the elevation of the concentration or the prolongation of the exposure times.However, when the concentration were between 10(-7) mol/L to 10(-4) mol/L, the inhibitory ratio rise progressively as the elevation of the concentration at all exposure times. The inhibitory ratio were 53.52%, 60.23%, 89.81% and 96.47% respectively when cells were treated by 10(-7), 10(-6), 10(-5) mol/L and 10(-4) mol/L mitomycin C for 72 h. An apparent "threshold dose effect" was observed in the paclitaxel treated groups.It's worth noting that the inhibitory ratio was only 48.22% when the cells had already been treated by 10(-5) mol/L paclitaxel for 72 h.However, when the concentration had reached 10(-4) mol/L, the inhibitory ratio sharply climbed to 93.38% even the cells had only been treated for 24 h. And the inhibitory ratio continued to rise as time prolonged. The results of cell apoptosis were consistent with MTT.When a significant inhibitory effect were detected by MTT, remarkable cell apoptosis could be observed by flow cytometry, and typical apoptotic cell could be identified by Hoechst 33342 fluorescent staining.
A certain concentration of mitomycin C or paclitaxel can inhibit Human Pulmonary Fibroblast proliferation in vitro. Both of these two drugs have potential value for the preparation of drug eluting airway stents. In order to ensure the inhibitory effect, the eluting concentration of mitomycin C and paclitaxel should not be less than 10(-7) mol/L and 10(-5) mol/L. But the eluting concentration of these two drugs should not exceed 10(-4) mol/L when both of the inhibitory ratio of these two drugs were higher than 95%.On this basis, elevating the drug concentration has little significance for improving the inhibitory effect, but increase the risk of systemic toxicity. Inducing cell apoptosis is one of the potential mechanisms of mitomycin C and paclitaxel in inhibiting cell proliferation.
观察丝裂霉素C和紫杉醇对人肺成纤维细胞体外增殖的抑制作用及其潜在机制,为药物洗脱气道支架的设计提供实验参考。
分别用浓度为10⁻¹¹mol/L至10⁻⁴mol/L的丝裂霉素C或紫杉醇作用于人肺成纤维细胞24、48或72小时后,采用MTT法检测细胞活力。分别用浓度为5×10⁻⁶、10⁻⁵、5×10⁻⁵、10⁻⁴、2×10⁻⁴mol/L的丝裂霉素C或紫杉醇作用于人肺成纤维细胞48小时后,采用膜联蛋白V-FITC和碘化丙啶双染,通过流式细胞术评估细胞凋亡情况。并用Hoechst 33342荧光染色观察细胞凋亡的形态学特征。
MTT结果显示,在所有浓度和作用时间下,丝裂霉素C和紫杉醇均能抑制细胞增殖。其中,当浓度在10⁻¹¹mol/L至10⁻⁸mol/L之间时,丝裂霉素C的抑制作用较弱,在此范围内,抑制率与浓度升高或作用时间延长不相关。然而,当浓度在10⁻⁷mol/L至10⁻⁴mol/L之间时,在所有作用时间下,抑制率均随浓度升高而逐渐升高。当细胞分别用10⁻⁷、10⁻⁶、10⁻⁵mol/L和10⁻⁴mol/L的丝裂霉素C处理72小时后,抑制率分别为53.52%、60.23%、89.81%和96.47%。在紫杉醇处理组中观察到明显的“阈值剂量效应”。值得注意的是,当细胞用10⁻⁵mol/L紫杉醇处理72小时后,抑制率仅为48.22%。然而,当浓度达到10⁻⁴mol/L时,即使细胞仅处理24小时,抑制率也急剧攀升至93.38%,且抑制率随时间延长继续升高。细胞凋亡结果与MTT结果一致。当MTT检测到显著抑制作用时,流式细胞术可观察到明显的细胞凋亡,Hoechst 33342荧光染色可鉴定出典型的凋亡细胞。
一定浓度的丝裂霉素C或紫杉醇可抑制人肺成纤维细胞体外增殖。这两种药物在制备药物洗脱气道支架方面均具有潜在价值。为确保抑制效果,丝裂霉素C和紫杉醇的洗脱浓度不应低于10⁻⁷mol/L和10⁻⁵mol/L。但当两种药物的抑制率均高于95%时,这两种药物的洗脱浓度不应超过10⁻⁴mol/L。在此基础上,提高药物浓度对提高抑制效果意义不大,但会增加全身毒性风险。诱导细胞凋亡是丝裂霉素C和紫杉醇抑制细胞增殖的潜在机制之一。