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施万细胞凋亡与p75神经营养因子受体(p75(NTR))小干扰RNA

Schwann cell apoptosis and p75(NTR) siRNA.

作者信息

Firouzi Masoumeh, Sabouni Farzaneh, Deezagi Abdolkhaleg, Pirbasti Zahra Hassannejad, Poorrajab Fatemeh, Rahimi-Movaghar Vafa

机构信息

Department of Biochemistry, National Institute of Genetic Engineering and Biotechnology, Tehran, Iran.

出版信息

Iran J Allergy Asthma Immunol. 2011 Mar;10(1):53-9.

Abstract

The p75 pan-neurotrophin receptor (p75(NTR)) plays a pivotal role in linking the immune system with the nervous system. p75(NTR) is required for the development of several characteristic features of allergic asthma. Also p75(NTR) upregulated by reactive Schwann cells after peripheral nerve injury. Moreover p75(NTR) and RhoA play a critical role in the regulation of apoptosis. To determine whether the designed siRNA for p75(NTR) can downregulates both p75(NTR) and Rho-A at RNA level in rats and, if so, at what magnitude, Schwann cell apoptosis occurs. Isolation and purification of neonate Schwann cells were prepared from rat sciatic nerve. Specific siRNA duplex was designed for p75(NTR) . To investigate the role of siRNA-mediated knockdown of p75(NTR) , the gene expression in p75(NTR) was examined with reverse transcription-polymerase chain reaction (RT-PCR) and Real-Time RT-PCR. Schwann cell apoptosis was performed by Annexin and TUNEL assays after 24 hours. Following p75(NTR) Transfection siRNA, p75(NTR) gene, compared with control, was downregulated by 73%. Without using siRNA for Rho-A, Rho-A gene was downregulated by 89% at the same time. Based on Annexin assay, apoptosis of Schwann cells occurred in siRNA+NGF and control+NGF by 16.76%±2.27 and 92.39%±1.82, respectively. TUNEL data showed that apoptosis of Schwann cells occurred in siRNA and control by 12.91%±6.39 and 78.55%±11.85, respectively. Thus, p75-siRNA downregulated both p75(NTR) and Rho-A at RNA level in rats and showed a role on decreased cell apoptosis compared to the controls.

摘要

p75泛神经营养因子受体(p75(NTR))在连接免疫系统和神经系统方面发挥着关键作用。p75(NTR)是过敏性哮喘若干特征发展所必需的。此外,外周神经损伤后,反应性雪旺细胞会使p75(NTR)上调。而且,p75(NTR)和RhoA在细胞凋亡调控中起关键作用。为了确定设计的针对p75(NTR)的小干扰RNA(siRNA)是否能在RNA水平下调大鼠体内的p75(NTR)和Rho - A,若能下调,下调幅度如何,以及雪旺细胞凋亡是否会发生。从大鼠坐骨神经制备新生雪旺细胞的分离和纯化。针对p75(NTR)设计了特异性siRNA双链体。为了研究siRNA介导的p75(NTR)敲低的作用,用逆转录 - 聚合酶链反应(RT - PCR)和实时RT - PCR检测p75(NTR)中的基因表达。24小时后通过膜联蛋白和TUNEL检测进行雪旺细胞凋亡检测。转染p75(NTR) siRNA后,与对照组相比,p75(NTR)基因下调了73%。在未使用针对Rho - A的siRNA的情况下,Rho - A基因同时下调了89%。基于膜联蛋白检测,siRNA + NGF组和对照组 + NGF组雪旺细胞凋亡率分别为16.76%±2.27和92.39%±1.82。TUNEL数据显示,siRNA组和对照组雪旺细胞凋亡率分别为12.91%±6.39和78.55%±11.85。因此,p75 - siRNA在RNA水平下调了大鼠体内的p75(NTR)和Rho - A,与对照组相比,显示出降低细胞凋亡的作用。

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