轉(zhuǎn)錄因子ZBTB38靶向修復(fù)繼發(fā)性脊髓損傷的機(jī)制研究
【文章頁數(shù)】:125 頁
【學(xué)位級(jí)別】:博士
【部分圖文】:
圖1.TG誘導(dǎo)SH-SY5Y細(xì)胞內(nèi)質(zhì)網(wǎng)應(yīng)激的發(fā)生(A)1μMTG處理SH-SY5Y24h后QRT-PCR的實(shí)驗(yàn)結(jié)果;(B)TG處理后與對(duì)照組相比細(xì)胞凋亡率檢測(cè);p*<0.05,p**<0.01
圖1.TG誘導(dǎo)SH-SY5Y細(xì)胞內(nèi)質(zhì)網(wǎng)應(yīng)激的發(fā)生(A)1μMTG處理SH-SY5Y24h后QRT-PCR的實(shí)驗(yàn)結(jié)果;(B)TG處理后與對(duì)照組相比細(xì)胞凋亡率檢測(cè);p*<0.05,p**<0.01。N(C)DMSO對(duì)照組;TG:TG處理實(shí)驗(yàn)組。Figure1.TG....
圖2.ZBTB38敲低后的SH-SY5Y細(xì)胞增殖與活率下降(A)3條ZBTB38siRNA(siRNA1、siRNA2和siRNA3)轉(zhuǎn)染SH-SY5Y細(xì)胞72h后WesternBlot的實(shí)驗(yàn)結(jié)果;(B)基于β-actin的WesternBlot灰度值比對(duì)分析結(jié)果;(C)細(xì)胞增殖率
圖1.TG誘導(dǎo)SH-SY5Y細(xì)胞內(nèi)質(zhì)網(wǎng)應(yīng)激的發(fā)生A)1μMTG處理SH-SY5Y24h后QRT-PCR的實(shí)驗(yàn)結(jié)果;(B)TG處理后與對(duì)照組相比胞凋亡率檢測(cè);p*<0.05,p**<0.01。N(C)DMSO對(duì)照組;TG:TG處理實(shí)驗(yàn)組。Figure1.TGin....
圖3.ZBTB38表達(dá)下調(diào)加劇了SH-SY5Y細(xì)胞的促凋亡(A)ZBTB38敲低后Westernblot檢測(cè)結(jié)果;(B)基于GAPDH的Westernblot結(jié)果灰度值比值分析;(C)ZBTB38敲低后促凋亡基因的QRT-PCR結(jié)果
圖3.ZBTB38表達(dá)下調(diào)加劇了SH-SY5Y細(xì)胞的促凋亡A)ZBTB38敲低后Westernblot檢測(cè)結(jié)果;(B)基于GAPDH的Westernblot結(jié)果灰度值分析;(C)ZBTB38敲低后促凋亡基因的QRT-PCR結(jié)果。NC,NC-1,NC-2:空載siRNSH....
圖5ZBTB38敲低后SH-SY5Y細(xì)胞中自噬小體的形成被抑制
圖5ZBTB38敲低后SH-SY5Y細(xì)胞中自噬小體的形成被抑制。白色箭頭指示自噬小體.Figure5.Transmissionelectronmicroscopyshowedthatthereweresignificantlylessphagosomesp....
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