慢病毒介導(dǎo)的shRNA干擾人C1GALT1胃癌穩(wěn)定細(xì)胞株的建立及其生物學(xué)特性
發(fā)布時間:2021-04-10 12:16
目的:構(gòu)建特異的靶向人C1GALT1基因的RNA干擾(RNAinterference,RNAi)慢病毒載體,建立C1GALT1基因穩(wěn)定沉默的胃癌MGC803細(xì)胞株。對慢病毒介導(dǎo)的shRNA靶向干擾C1GALT1胃癌MGC803穩(wěn)定細(xì)胞株生物學(xué)特性進行初步觀察,檢測沉默C1GALT1基因表達(dá)對MGC803細(xì)胞增殖、遷移、侵襲、周期、凋亡功能的影響。方法:1.設(shè)計C1GALT1基因的特異性shRNA靶點,構(gòu)建pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1干擾慢病毒包裝載體,包裝慢病毒并侵染MGC803細(xì)胞,構(gòu)建C1GALT1基因穩(wěn)定沉默的胃癌MGC803細(xì)胞株。用轉(zhuǎn)染空載體的穩(wěn)轉(zhuǎn)細(xì)胞作為陰性對照。采用qPCR方法檢測MGC803細(xì)胞中C1GALT1的mRNA水平變化,Western Blot方法檢測C1GALT1蛋白水平的表達(dá),以鑒定C1GALT1基因沉默的效果。2.采用CCK8增殖實驗、細(xì)胞劃痕實驗、Transwell實驗、流式細(xì)胞術(shù)檢測C1GALT1基因沉默后對胃癌MGC803細(xì)胞的增殖、遷移、侵襲、周期、凋亡能力的影響。結(jié)果:1.成功構(gòu)建了特異...
【文章來源】:南華大學(xué)湖南省
【文章頁數(shù)】:60 頁
【學(xué)位級別】:碩士
【部分圖文】:
h-C1GALT1shRNA1測序結(jié)果比對圖(綠色區(qū)域為與目的序列匹配部分)
17第三章實驗結(jié)果3.1pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1重組質(zhì)粒的構(gòu)建和測序鑒定將siRNA1單鏈的引物退火,再連接入雙酶切線性化的RNA干擾載體(pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO)中,挑選菌落送至測序公司進行測序,測序結(jié)果正確(見圖3.1,3.2),證明構(gòu)建pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1重組質(zhì)粒成功。圖3.1h-C1GALT1shRNA1測序結(jié)果比對圖(綠色區(qū)域為與目的序列匹配部分)圖3.2測序峰圖3.2pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1慢病毒感染MGC803細(xì)胞及構(gòu)建穩(wěn)定沉默細(xì)胞系將pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1慢病毒感染人胃癌MGC803細(xì)胞,并添加助感染試劑增加感染率,再進行C1GALT1基因穩(wěn)定沉默的胃癌MGC803細(xì)胞的單克隆培養(yǎng),使用Puromycin篩選感染細(xì)胞,然后對其放大培養(yǎng),用倒置熒光顯微鏡觀察細(xì)胞呈現(xiàn)出綠色熒光,表明穩(wěn)定感染的細(xì)胞株構(gòu)建成功。
18單克隆MGC803-h-C1GALT1干擾擴大培養(yǎng)后的熒光圖,選取1個視野進行熒光和白光拍照,結(jié)果如下:見圖3.3。圖3.3MGC-803細(xì)胞系中沉默C1GALT1表達(dá)的細(xì)胞株(×20)3.3ReRlRRmePCR法檢測C1GALT1表達(dá)結(jié)果C1GALT1基因穩(wěn)定沉默細(xì)胞系MGC-803中經(jīng)過單克隆培養(yǎng)及篩選最終挑取MGC803-sh-C1GALT1-1、MGC803-sh-C1GALT1-2、MGC803-sh-C1GALT1-3這3株細(xì)胞,和空載體組細(xì)胞(MGC-803-NC)一共4株分別進行RNA提取,利用紫外分光光度計其質(zhì)量,見表3.1。使用實時熒光定量PCR儀進行熒光定量PCR反應(yīng)并繪制溶解曲線及擴增曲線,GAPDH和h-C1GALT1溶解曲線較好,證明RNA抽提和QPCR過程無問題,見圖3.4、3.5。C1GALT1基因穩(wěn)定沉默組的C1GALT1的mRNA比陰性對照組明顯降低(p<0.05),h-C1GALT1在MGC-803細(xì)胞中有干擾效果,其中C1GALT1-shRNA1單克隆3干擾下調(diào)73%,見圖3.6。表3.1紫外分光光度計檢測RNA提取質(zhì)量檢測結(jié)果樣品名稱OD260/OD280OD260/OD230RNA濃度(ng/uL)MGC-803-NC1.911.99546sh-C1GALT1-11.891.96560sh-C1GALT1-21.861.94551sh-C1GALT1-31.881.95544
【參考文獻(xiàn)】:
期刊論文
[1]Long noncoding RNA HOXA11-AS promotes gastric cancer cell proliferation and invasion via SRSF1 and functions as a biomarker in gastric cancer[J]. Yun Liu,Yu-Mei Zhang,Feng-Bo Ma,Su-Rong Pan,Bao-Zhen Liu. World Journal of Gastroenterology. 2019(22)
[2]Prognostic significance of preoperative and postoperative CK19 and CEA m RNA levels in peripheral blood of patients with gastric cardia cancer[J]. Yu-Feng Qiao,Chuan-Gui Chen,Jie Yue,Ming-Quan Ma,Zhao Ma,Zhen-Tao Yu. World Journal of Gastroenterology. 2017(08)
[3]New advances in targeted gastric cancer treatment[J]. Daniela Cornelia Laz?r,Sorina T?ban,Marioara Cornianu,Alexandra Faur,Adrian Goldi?. World Journal of Gastroenterology. 2016(30)
[4]Nitrosamine and related food intake and gastric and oesophageal cancer risk: A systematic review of the epidemiological evidence[J]. Paula Jakszyn,Carlos Alberto González. World Journal of Gastroenterology. 2006(27)
本文編號:3129623
【文章來源】:南華大學(xué)湖南省
【文章頁數(shù)】:60 頁
【學(xué)位級別】:碩士
【部分圖文】:
h-C1GALT1shRNA1測序結(jié)果比對圖(綠色區(qū)域為與目的序列匹配部分)
17第三章實驗結(jié)果3.1pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1重組質(zhì)粒的構(gòu)建和測序鑒定將siRNA1單鏈的引物退火,再連接入雙酶切線性化的RNA干擾載體(pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO)中,挑選菌落送至測序公司進行測序,測序結(jié)果正確(見圖3.1,3.2),證明構(gòu)建pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1重組質(zhì)粒成功。圖3.1h-C1GALT1shRNA1測序結(jié)果比對圖(綠色區(qū)域為與目的序列匹配部分)圖3.2測序峰圖3.2pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1慢病毒感染MGC803細(xì)胞及構(gòu)建穩(wěn)定沉默細(xì)胞系將pHBLV-U6-MCS-CMV-ZsGreen-PGK-PURO-h-C1GALT1慢病毒感染人胃癌MGC803細(xì)胞,并添加助感染試劑增加感染率,再進行C1GALT1基因穩(wěn)定沉默的胃癌MGC803細(xì)胞的單克隆培養(yǎng),使用Puromycin篩選感染細(xì)胞,然后對其放大培養(yǎng),用倒置熒光顯微鏡觀察細(xì)胞呈現(xiàn)出綠色熒光,表明穩(wěn)定感染的細(xì)胞株構(gòu)建成功。
18單克隆MGC803-h-C1GALT1干擾擴大培養(yǎng)后的熒光圖,選取1個視野進行熒光和白光拍照,結(jié)果如下:見圖3.3。圖3.3MGC-803細(xì)胞系中沉默C1GALT1表達(dá)的細(xì)胞株(×20)3.3ReRlRRmePCR法檢測C1GALT1表達(dá)結(jié)果C1GALT1基因穩(wěn)定沉默細(xì)胞系MGC-803中經(jīng)過單克隆培養(yǎng)及篩選最終挑取MGC803-sh-C1GALT1-1、MGC803-sh-C1GALT1-2、MGC803-sh-C1GALT1-3這3株細(xì)胞,和空載體組細(xì)胞(MGC-803-NC)一共4株分別進行RNA提取,利用紫外分光光度計其質(zhì)量,見表3.1。使用實時熒光定量PCR儀進行熒光定量PCR反應(yīng)并繪制溶解曲線及擴增曲線,GAPDH和h-C1GALT1溶解曲線較好,證明RNA抽提和QPCR過程無問題,見圖3.4、3.5。C1GALT1基因穩(wěn)定沉默組的C1GALT1的mRNA比陰性對照組明顯降低(p<0.05),h-C1GALT1在MGC-803細(xì)胞中有干擾效果,其中C1GALT1-shRNA1單克隆3干擾下調(diào)73%,見圖3.6。表3.1紫外分光光度計檢測RNA提取質(zhì)量檢測結(jié)果樣品名稱OD260/OD280OD260/OD230RNA濃度(ng/uL)MGC-803-NC1.911.99546sh-C1GALT1-11.891.96560sh-C1GALT1-21.861.94551sh-C1GALT1-31.881.95544
【參考文獻(xiàn)】:
期刊論文
[1]Long noncoding RNA HOXA11-AS promotes gastric cancer cell proliferation and invasion via SRSF1 and functions as a biomarker in gastric cancer[J]. Yun Liu,Yu-Mei Zhang,Feng-Bo Ma,Su-Rong Pan,Bao-Zhen Liu. World Journal of Gastroenterology. 2019(22)
[2]Prognostic significance of preoperative and postoperative CK19 and CEA m RNA levels in peripheral blood of patients with gastric cardia cancer[J]. Yu-Feng Qiao,Chuan-Gui Chen,Jie Yue,Ming-Quan Ma,Zhao Ma,Zhen-Tao Yu. World Journal of Gastroenterology. 2017(08)
[3]New advances in targeted gastric cancer treatment[J]. Daniela Cornelia Laz?r,Sorina T?ban,Marioara Cornianu,Alexandra Faur,Adrian Goldi?. World Journal of Gastroenterology. 2016(30)
[4]Nitrosamine and related food intake and gastric and oesophageal cancer risk: A systematic review of the epidemiological evidence[J]. Paula Jakszyn,Carlos Alberto González. World Journal of Gastroenterology. 2006(27)
本文編號:3129623
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