首页> 外文期刊>Journal of biomedical science. >LncRNA {'type':'entrez-nucleotide','attrs':{'text':'DQ786243','term_id':'110631570','term_text':'DQ786243'}}DQ7
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LncRNA {'type':'entrez-nucleotide','attrs':{'text':'DQ786243','term_id':'110631570','term_text':'DQ786243'}}DQ7

机译:LncRNA {“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id”:“ 110631570”,“ term_text”:“ DQ786243”}}} DQ7

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BackgroundLong non-coding RNAs (lncRNAs) have different functions in cells. They work as signals, decoys, guides, and scaffolds. Altered lncRNA levels can affect the expression of gene products. There are seldom studies on the role of lncRNAs in inflammatory bowel disease (IBD).ResultsQuantitative RT-PCR showed that {"type":"entrez-nucleotide","attrs":{"text":"DQ786243","term_id":"110631570","term_text":"DQ786243"}}DQ786243 was significantly overexpressed in clinical active CD patients compared with clinical inactive CD patients (P?=?0.0118) or healthy controls (P?=?0.002). CREB was also more highly expressed in active CD than in inactive CD (P?=?0.0034) or controls (P?=?0.0241). Foxp3 was interestingly lower in inactive CD than in active CD (P?=?0.0317) or controls (P?=?0.0103), but there were no apparent differences between active CD and controls. CRP was well correlated with {"type":"entrez-nucleotide","attrs":{"text":"DQ786243","term_id":"110631570","term_text":"DQ786243"}}DQ786243 (r?=?0.489, P?=?0.034), CREB (r?=?0.500, P?=?0.029) and Foxp3 (r?=?0.546, P?=?0.016). At 48?hours after {"type":"entrez-nucleotide","attrs":{"text":"DQ786243","term_id":"110631570","term_text":"DQ786243"}}DQ786243 transfection, qRT-PCR showed both CREB (P?=?0.017) and Foxp3 (P?=?0.046) had an increased mRNA expression in Jurkat cells. Western blot showed the same pattern. After {"type":"entrez-nucleotide","attrs":{"text":"DQ786243","term_id":"110631570","term_text":"DQ786243"}}DQ786243 transfection, CREB phosphorylation ratio (p-CREB/t-CREB) was increased (P?=?0.0043).Conclusion{"type":"entrez-nucleotide","attrs":{"text":"DQ786243","term_id":"110631570","term_text":"DQ786243"}}DQ786243 can be related with severity of CD. It can affect the expression of CREB and Foxp3 through which regulates the function of Treg. CREB itself seems not the mediator of {"type":"entrez-nucleotide","attrs":{"text":"DQ786243","term_id":"110631570","term_text":"DQ786243"}}DQ786243 to up-regulate Foxp3. The phosphorylation of CREB might play a more important role in the process.
机译:背景长非编码RNA(lncRNA)在细胞中具有不同的功能。它们充当信号,诱饵,指南和脚手架。改变的lncRNA水平会影响基因产物的表达。关于lncRNA在炎症性肠病(IBD)中的作用的研究很少。结果定量RT-PCR显示{“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id” :“ 110631570”,“ term_text”:“ DQ786243”}} DQ786243在临床活动性CD患者中明显高于临床非活动性CD患者(P <= 0.0118)或健康对照组(P <= 0.002)。 CREB在活性CD中的表达也比无活性CD(P = 0.0034)或对照(P = 0.0241)高。有趣的是,非活性CD中的Foxp3低于活性CD(P≥0.0317)或对照组(P≥0.0103),但是活性CD与对照之间没有明显差异。 CRP与{“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id”:“ 110631570”,“ term_text”:“ DQ786243”}} DQ786243(r? = 0.489,P = 0.034,CREB(r = 0.500,P = 0.029)和Foxp3(r = 0.546,P = 0.016)。在{“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id”:“ 110631570”,“ term_text”:“ DQ786243”}} DQ786243转染,qRT后48小时-PCR表明,CREB(P≥0.017)和Foxp3(P = 0.046)在Jurkat细胞中均具有增加的mRNA表达。蛋白质印迹显示相同的模式。在{“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id”:“ 110631570”,“ term_text”:“ DQ786243”}}} DQ786243转染后,CREB磷酸化率(p -CREB ​​/ t-CREB)增加(P?=?0.0043)。结论{“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id”:“ 110631570”, “ term_text”:“ DQ786243”}} DQ786243与CD的严重程度有关。它可以影响CREB和Foxp3的表达,从而调节Treg的功能。 CREB本身似乎不是{“ type”:“ entrez-nucleotide”,“ attrs”:{“ text”:“ DQ786243”,“ term_id”:“ 110631570”,“ term_text”:“ DQ786243”}} DQ786243的介体上调Foxp3。 CREB的磷酸化可能在此过程中发挥更重要的作用。

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