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二硝基苯酚调节骨髓间充质干细胞中血管生成、细胞存活和心肌生成因子的基因表达水平。

Dinitrophenol modulates gene expression levels of angiogenic, cell survival and cardiomyogenic factors in bone marrow derived mesenchymal stem cells.

作者信息

Ali Anwar, Akhter Muhammad Aleem, Haneef Kanwal, Khan Irfan, Naeem Nadia, Habib Rakhshinda, Kabir Nurul, Salim Asmat

机构信息

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi-75270, Pakistan.

Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical and Biological Sciences, University of Karachi, Karachi-75270, Pakistan.

出版信息

Gene. 2015 Jan 25;555(2):448-57. doi: 10.1016/j.gene.2014.10.045. Epub 2014 Oct 28.

Abstract

Various preconditioning strategies influence regeneration properties of stem cells. Preconditioned stem cells generally show better cell survival, increased differentiation, enhanced paracrine effects, and improved homing to the injury site by regulating the expression of tissue-protective cytokines and growth factors. In this study, we analyzed gene expression pattern of growth factors through RT-PCR after treatment of mesenchymal stem cells (MSCs) with a metabolic inhibitor, 2,4 dinitrophenol (DNP) and subsequent re-oxygenation for periods of 2, 6, 12 and 24h. These growth factors play important roles in cardiomyogenesis, angiogenesis and cell survival. Mixed pattern of gene expression was observed depending on the period of re-oxygenation. Of the 13 genes analyzed, ankyrin repeat domain 1 (Ankrd1) and GATA6 were downregulated after DNP treatment and subsequent re-oxygenations. Ankrd1 expression was, however, increased after 24h of re-oxygenation. Placental growth factor (Pgf), endoglin (Eng), neuropilin (Nrp1) and jagged 1 (Jag1) were up-regulated after DNP treatment. Gradual increase was observed as re-oxygenation advances and by the end of the re-oxygenation period the expression started to decrease and ultimately regained normal values. Epiregulin (Ereg) was not expressed in normal MSCs but its expression increased gradually from 2 to 24h after re-oxygenation. No change was observed in the expression level of connective tissue growth factor (Ctgf) at any time period after re-oxygenation. Kindlin3, kinase insert domain receptor (Kdr), myogenin (Myog), Tbx20 and endothelial tyrosine kinase (Tek) were not expressed either in normal cells or cells treated with DNP. It can be concluded from the present study that MSCs adjust their gene expression levels under the influence of DNP induced metabolic stress. Their levels of expression vary with varying re-oxygenation periods. Preconditioning of MSCs with DNP can be used for enhancing the potential of these cells for better regeneration.

摘要

多种预处理策略会影响干细胞的再生特性。经过预处理的干细胞通常表现出更好的细胞存活率、增强的分化能力、更强的旁分泌效应,并且通过调节组织保护细胞因子和生长因子的表达,改善归巢至损伤部位的能力。在本研究中,我们在用代谢抑制剂2,4-二硝基苯酚(DNP)处理间充质干细胞(MSC)并随后分别复氧2小时、6小时、12小时和24小时后,通过逆转录聚合酶链反应(RT-PCR)分析了生长因子的基因表达模式。这些生长因子在心肌生成、血管生成和细胞存活中发挥重要作用。根据复氧时间的不同,观察到了基因表达的混合模式。在所分析的13个基因中,锚蛋白重复结构域1(Ankrd1)和GATA6在DNP处理及随后的复氧后表达下调。然而,复氧24小时后Ankrd1的表达增加。胎盘生长因子(Pgf)、内皮糖蛋白(Eng)、神经纤毛蛋白(Nrp1)和锯齿蛋白1(Jag1)在DNP处理后上调。随着复氧时间的延长观察到逐渐增加,到复氧期结束时,表达开始下降并最终恢复到正常值。表皮调节素(Ereg)在正常MSC中不表达,但复氧后2至24小时其表达逐渐增加。复氧后任何时间段内,结缔组织生长因子(Ctgf)的表达水平均未观察到变化。Kindlin3、激酶插入结构域受体(Kdr)、生肌调节因子(Myog)、Tbx20和内皮酪氨酸激酶(Tek)在正常细胞或用DNP处理的细胞中均未表达。从本研究可以得出结论,间充质干细胞在DNP诱导的代谢应激影响下会调整其基因表达水平。它们的表达水平随复氧时间的不同而变化。用DNP对间充质干细胞进行预处理可用于增强这些细胞更好再生的潜力。

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