MiR-21协同BMP9促进间充质干细胞C3H10T1/2成骨分化
发布时间:2021-11-26 20:17
目的:探讨miR-21与BMP9之间的关系,明确miR-21在BMP9诱导间充质干细胞成骨分化中的作用。方法:(1)Ad-BMP9感染C3H10T1/2细胞,Real-time-PCR检测miR-21表达。RTPCR检测ALP的表达。(2)MiR-21转染C3H10T1/2细胞,Real-time-PCR检测miR-21和BMP9表达。(3)MiR-21和BMP9-CM处理C3H10 T1/2细胞,ALP活性和染色实验检测C3H10 T1/2细胞早期成骨能力。茜素红S染色实验检测钙盐沉积情况。(4)MiR-21和BMP9-CM处理C3H10T1/2细胞,Real-time-PCR检测成骨分化相关因子ALP,OCN的表达。(5)MiR-21和BMP9-CM处理C3H10T1/2细胞,Western blot检测p-Smad1/5蛋白水平的表达。结果:(1)BMP9暂时降低miR-21的表达。MiR-21也可以暂时降低BMP9的表达。(2)MiR-21可以协同BMP9增强ALP和钙盐沉积。(3)MiR-21协同BMP9增加了p-Smad1/5蛋白水平的表达。结论:MiR-21与BMP9存在...
【文章来源】:中国生物工程杂志. 2016,36(02)北大核心CSCD
【文章页数】:8 页
【部分图文】:
miR-21在BMP9诱导C3H10T1/2细胞成骨分化中的表达Fig.1ThetemporarydownregulationofmiR-21duringBMP9-inducedosteogenicdifferentiationofC3H10T1/2cell(a)Ad-BMP9andAd-GFPcaninfectC3H10T1/2cell(×100)(b)ExpressionofALPdetectedbyRT-PCR(c)ExpressionofmiR-21*****
2016,36(2)宋琪玲等:MiR-21协同BMP9促进间充质干细胞C3H10T1/2成骨分化图2过表达miR-21,BMP9在C3H10T1/2细胞中的表达变化Fig.2ThetemporarydownregulationofBMP9mRNAbytransferringmiR-21intoC3H10T1/2cell(a)ExpressionofmiR-21detectedbyReal-timePCR***P<0.001comparedwithNCgroup(b)ExpressionofBMP9at1daydetectedbyReal-timePCR**P<0.01comparedwithNCgroup(c)ExpressionofBMP9at5daydetectedbyReal-timePCR*P<0.5comparedwithNCgroup图3miR-21促进了BMP9诱导的C3H10T1/2细胞早期成骨分化Fig.3OverexpressionmiR-21enhancesBMP9-inducedearlyosteogenicdifferentiantionofC3H10T1/2cell(a)ALPstainingresultswererecordedinhighermagnifications(×100)(b)ALPstainingresultswererecordedinlowermagnifications(c)ALPactivitydeterminedbyALPquantitativeassay*P<0.5comparedwithNC+BMP9group;**P<0.01comparedwithmiR-21group25
2016,36(2)宋琪玲等:MiR-21协同BMP9促进间充质干细胞C3H10T1/2成骨分化图2过表达miR-21,BMP9在C3H10T1/2细胞中的表达变化Fig.2ThetemporarydownregulationofBMP9mRNAbytransferringmiR-21intoC3H10T1/2cell(a)ExpressionofmiR-21detectedbyReal-timePCR***P<0.001comparedwithNCgroup(b)ExpressionofBMP9at1daydetectedbyReal-timePCR**P<0.01comparedwithNCgroup(c)ExpressionofBMP9at5daydetectedbyReal-timePCR*P<0.5comparedwithNCgroup图3miR-21促进了BMP9诱导的C3H10T1/2细胞早期成骨分化Fig.3OverexpressionmiR-21enhancesBMP9-inducedearlyosteogenicdifferentiantionofC3H10T1/2cell(a)ALPstainingresultswererecordedinhighermagnifications(×100)(b)ALPstainingresultswererecordedinlowermagnifications(c)ALPactivitydeterminedbyALPquantitativeassay*P<0.5comparedwithNC+BMP9group;**P<0.01comparedwithmiR-21group25
【参考文献】:
期刊论文
[1]TGF-β/BMP signaling and other molecular events: regulation of osteoblastogenesis and bone formation[J]. Md Shaifur Rahman,Naznin Akhtar,Hossen Mohammad Jamil,Rajat Suvra Banik,Sikder M Asaduzzaman. Bone Research. 2015(01)
[2]Spry1在miR-21调控人骨髓间充质干细胞成骨分化中的作用[J]. 杨楠,周威,王光,丁寅,金岩. 中国组织工程研究. 2014(32)
[3]miR-30a抑制BMP9诱导间充质干细胞C3H10T1/2的成骨分化[J]. 李宝林,白慧丽,张汝益,严树涓,何方,杨丹丹,刘晨,施琼. 中国生物工程杂志. 2013(11)
本文编号:3520853
【文章来源】:中国生物工程杂志. 2016,36(02)北大核心CSCD
【文章页数】:8 页
【部分图文】:
miR-21在BMP9诱导C3H10T1/2细胞成骨分化中的表达Fig.1ThetemporarydownregulationofmiR-21duringBMP9-inducedosteogenicdifferentiationofC3H10T1/2cell(a)Ad-BMP9andAd-GFPcaninfectC3H10T1/2cell(×100)(b)ExpressionofALPdetectedbyRT-PCR(c)ExpressionofmiR-21*****
2016,36(2)宋琪玲等:MiR-21协同BMP9促进间充质干细胞C3H10T1/2成骨分化图2过表达miR-21,BMP9在C3H10T1/2细胞中的表达变化Fig.2ThetemporarydownregulationofBMP9mRNAbytransferringmiR-21intoC3H10T1/2cell(a)ExpressionofmiR-21detectedbyReal-timePCR***P<0.001comparedwithNCgroup(b)ExpressionofBMP9at1daydetectedbyReal-timePCR**P<0.01comparedwithNCgroup(c)ExpressionofBMP9at5daydetectedbyReal-timePCR*P<0.5comparedwithNCgroup图3miR-21促进了BMP9诱导的C3H10T1/2细胞早期成骨分化Fig.3OverexpressionmiR-21enhancesBMP9-inducedearlyosteogenicdifferentiantionofC3H10T1/2cell(a)ALPstainingresultswererecordedinhighermagnifications(×100)(b)ALPstainingresultswererecordedinlowermagnifications(c)ALPactivitydeterminedbyALPquantitativeassay*P<0.5comparedwithNC+BMP9group;**P<0.01comparedwithmiR-21group25
2016,36(2)宋琪玲等:MiR-21协同BMP9促进间充质干细胞C3H10T1/2成骨分化图2过表达miR-21,BMP9在C3H10T1/2细胞中的表达变化Fig.2ThetemporarydownregulationofBMP9mRNAbytransferringmiR-21intoC3H10T1/2cell(a)ExpressionofmiR-21detectedbyReal-timePCR***P<0.001comparedwithNCgroup(b)ExpressionofBMP9at1daydetectedbyReal-timePCR**P<0.01comparedwithNCgroup(c)ExpressionofBMP9at5daydetectedbyReal-timePCR*P<0.5comparedwithNCgroup图3miR-21促进了BMP9诱导的C3H10T1/2细胞早期成骨分化Fig.3OverexpressionmiR-21enhancesBMP9-inducedearlyosteogenicdifferentiantionofC3H10T1/2cell(a)ALPstainingresultswererecordedinhighermagnifications(×100)(b)ALPstainingresultswererecordedinlowermagnifications(c)ALPactivitydeterminedbyALPquantitativeassay*P<0.5comparedwithNC+BMP9group;**P<0.01comparedwithmiR-21group25
【参考文献】:
期刊论文
[1]TGF-β/BMP signaling and other molecular events: regulation of osteoblastogenesis and bone formation[J]. Md Shaifur Rahman,Naznin Akhtar,Hossen Mohammad Jamil,Rajat Suvra Banik,Sikder M Asaduzzaman. Bone Research. 2015(01)
[2]Spry1在miR-21调控人骨髓间充质干细胞成骨分化中的作用[J]. 杨楠,周威,王光,丁寅,金岩. 中国组织工程研究. 2014(32)
[3]miR-30a抑制BMP9诱导间充质干细胞C3H10T1/2的成骨分化[J]. 李宝林,白慧丽,张汝益,严树涓,何方,杨丹丹,刘晨,施琼. 中国生物工程杂志. 2013(11)
本文编号:3520853
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