夏春輝,王玉,陳宇航,孫東升,付雙,李紅梅
齊齊哈爾醫(yī)學(xué)院藥學(xué)院,黑龍江齊齊哈爾161006
MTT法檢測(cè)異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用
夏春輝,王玉,陳宇航,孫東升,付雙,李紅梅
齊齊哈爾醫(yī)學(xué)院藥學(xué)院,黑龍江齊齊哈爾161006
目的研究異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用。方法采用四甲基偶氮唑藍(lán)染色法(MTT法)測(cè)定異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用。結(jié)果異咯嗪光動(dòng)力能明顯抑制Bel-7402細(xì)胞。結(jié)論異咯嗪是一種很有潛力抗癌光敏劑。
異咯嗪;光動(dòng)力;凋亡;Bel-7402細(xì)胞
腫瘤光動(dòng)力治療(photodynamic therapy)是一種新型的治療腫瘤技術(shù)。該技術(shù)是基于特定波長(zhǎng)的光激發(fā)腫瘤細(xì)胞攝入的光敏劑,生成活性很強(qiáng)的活性氧,從而殺死腫瘤細(xì)胞[1-3]。光敏劑是光動(dòng)力治療的關(guān)鍵。由于異咯嗪毒副作用小,表現(xiàn)出較強(qiáng)的光敏特性,因而它可能是很有前途的抗腫瘤光敏劑[4-6]。該文采用四甲基偶氮唑藍(lán)染色法(MTT染色法)研究了異咯嗪(結(jié)構(gòu)見(jiàn)圖1)光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用,以期為其臨床應(yīng)用奠定基礎(chǔ)。
1.1 材料
異咯嗪與MTT為Sigma公司產(chǎn)品;DMEM培養(yǎng)基Gibco公司產(chǎn)品;牛血清為PAA公司產(chǎn)品;其他試劑為國(guó)產(chǎn)分析純;Bel-7402人肝癌細(xì)胞為哈爾濱醫(yī)科大學(xué)腫瘤研究所提供。
1.2 儀器及設(shè)備
VS-1300L-U凈化工作臺(tái);3111二氧化碳培養(yǎng)箱;SB-100P黑光燈;DSZ-5000X倒置生物顯微鏡,680全自動(dòng)酶標(biāo)儀。
1.3 細(xì)胞培養(yǎng)
在37℃,含5%CO2的培養(yǎng)箱內(nèi),Bel-7402人肝癌細(xì)胞用含10%小牛血清的DMEM培養(yǎng)基(鏈霉素與青霉素的終濃度為100 mg/L)培養(yǎng)。
1.4 MTT染色法測(cè)定異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用
取對(duì)數(shù)生長(zhǎng)期細(xì)胞,胰蛋白酶消化后,調(diào)整濃度約為4×104個(gè)/mL,然后接種于96孔培養(yǎng)板中。在培養(yǎng)孔中加入濃度為4 μg/mL的異咯嗪新培養(yǎng)液,用SB-100P燈照射60 min。在37℃下加入PBS配制的MTT溶液(5 g/L),培養(yǎng)4 h,在倒置顯微鏡下觀察經(jīng)異咯嗪光動(dòng)力作用后的細(xì)胞。吸取上清,加入200 μL DMSO,在波長(zhǎng)570 nm處測(cè)定吸光度值A(chǔ)。然后根據(jù)公式:細(xì)胞抑制率=(1-A實(shí)驗(yàn)孔/A空白對(duì)照孔)×100%進(jìn)行計(jì)算。
圖1 異咯嗪光敏劑的結(jié)構(gòu)
MTT法研究了異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制率影響。圖2顯示異咯嗪光動(dòng)力能明顯抑制Bel-7402細(xì)胞,在光照60 min后,異咯嗪表現(xiàn)出對(duì)Bel-7402細(xì)胞極強(qiáng)的殺傷能力,其抑制率達(dá)到70%左右。此外,MTT染色顯示:未經(jīng)異咯嗪光動(dòng)力處理的Bel-7402細(xì)胞MTT染色后,在細(xì)胞內(nèi)及細(xì)胞周?chē)煞植急容^均勻的紫藍(lán)色Formazan結(jié)晶(圖3A);而B(niǎo)el-7402細(xì)胞經(jīng)過(guò)經(jīng)異咯嗪光動(dòng)力作用后,細(xì)胞數(shù)目明顯降低,細(xì)胞結(jié)構(gòu)遭到破壞,細(xì)胞失去了還原MTT能力,導(dǎo)致紫藍(lán)色結(jié)晶明顯減少,細(xì)胞處于調(diào)亡和壞死狀態(tài)(圖3B)。
圖2 MTT法分析異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制率
圖3 MTT染色分析異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用
一些研究顯示異咯嗪光動(dòng)力對(duì)腫瘤細(xì)胞的抑制作用[7-8],然而異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞的抑制作用還鮮見(jiàn)報(bào)道。因此,在該研究通過(guò)MTT染色法研究了異咯嗪光動(dòng)力對(duì)Bel-7402細(xì)胞作用。結(jié)果顯示,異咯嗪光動(dòng)力能明顯抑制Bel-7402細(xì)胞增殖。作用機(jī)理可能是:腫瘤細(xì)胞攝入的異咯嗪(A)在特定波長(zhǎng)激發(fā)后,通過(guò)系間竄躍,基態(tài)的A變?yōu)榧ぐl(fā)三線態(tài)(3A*);3A*與H2O和O2反應(yīng),或與三線態(tài)氧(3O2)反應(yīng),產(chǎn)生過(guò)氧化氫(H2O2)、羥自由基(·OH)、超氧負(fù)離子自由基(·O-2)、單線態(tài)氧(1O2)等活性氧(reactive oxygen species,ROS);ROS與細(xì)胞膜內(nèi)外的生物大分子(如蛋白質(zhì)、酶類(lèi)和脂類(lèi)等)發(fā)生氧化反應(yīng),從而導(dǎo)致Bel-7402細(xì)胞凋亡或壞死。該過(guò)程可用如下反應(yīng)式表示:
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Inhibition Effect of MTT Method in Detecting the Isoalloxazine Photodynamic on the Bel-7402 Cells
XIA Chun-hui,WANG Yu,CHEN Yu-hang,SUN Dong-sheng,FU Shuang,LI Hong-mei
Pharmacy College,Qiqihar Medical University,Qiqihar,Heilongjiang Province,161006 China
ObjectiveTo research the inhibition effect of MTT method in detecting the isoalloxazine photodynamic on the Bel-7402 cells.MethodsThe inhibition effect of isoalloxazine photodynamic on the Bel-7402 cells was measured by the MTT method.ResultsThe isoalloxazine photodynamic can obviously inhibit the Bel-7402 cells.ConclusionIsoalloxazine is a potential photosensitizer.
Isoalloxazine;Photodynamic;Apoptosis;Bel-7402 cells
R735.7
A
1672-5654(2017)01(c)-0047-02
10.16659/j.cnki.1672-5654.2017.03.047
2016-10-23)
齊齊哈爾市科學(xué)技術(shù)計(jì)劃項(xiàng)目(SFGG-201206)。
夏春輝(1969.12-),男,黑龍江齊齊哈爾人,碩士,教授,研究方向:功能材料制備與抗腫瘤機(jī)制研究。