关键词： activating transcription factor 3   lentiviral vectors of overexpression   cytological mechanism   PROTEIN SUPPRESSES   SIGNALING PATHWAYS   PROSTATE-CANCER   RESPONSE GENE   UP-REGULATION   DNA-DAMAGE   ER STRESS   KEY ROLE   ATF3   EXPRESSION  

摘要： The present study observed and compared the biological behaviour of HepG2 cells prior and subsequent to the overexpression of activating transcription factor 3 (ATF3). Experiments investigating the cytological function by which ATF3 affects liver cancer cells were also performed. MTT, Transwell and flow cytometry assays were used to observe and detect the biological behaviour of HepG2 cells with and without lentivirus (LV)-ATF3-enhanced green fluorescent protein (EGFP) infection. The effects of ATF3 overexpression on cell proliferation, migration, apoptosis and cell cycle progression were evaluated. The LV-ATF3-EGFP overexpression vector was successfully constructed, and the HepG2 cells were successfully infected with the vector. Following ATF3 overexpression, cell proliferation was decreased, the rate of cell apoptosis was accelerated and cell cycle progression was slowed (P<0.05). There were no marked changes in cell migration (P>0.05), although there was a trend towards a gradual decrease. In conclusion, ATF3 exerted suppressive effects in HepG2 cells, potentially by inhibiting cancer cell growth, accelerating cell apoptosis, and blocking cell cycle progression. Intervention targeting ATF3 expression may represent a novel approach for the prevention and treatment of human liver cancer.

关键词： TRANSCRIPTION factors   PARTICULATE matter  

关键词： Spinal cord injury (SCI)   TREM1   Inflammation   Oxidative stress   HO-1   ANTIOXIDANT THERAPIES   FUNCTIONAL RECOVERY   MICROGLIA   ACTIVATION   PAIN   RESPONSES   ATF3  

摘要： Spinal cord injury (SCI) is a devastating event, leading to the progression of chronic neuropathic pain syndrome. Triggering receptor expressed on myeloid cells 1 (TREM1) is an innate immune receptor expressed on neutrophils and monocytes/macrophages. TREM1 enhances inflammatory response in various models of diseases, but its significance in SCI remains unclear. In the present study, we attempted to explore the effects of TREM1 on the regulation of SCI. Spinal cord contusion injury was performed in wild type (WT) and TREM1-knockout (TREM1(KO)) mice, and real time-quantitative PCR (RT-qPCR), western blot, and immunofluorescent (IF) staining were used to calculate TREM1, inflammation and oxidative stress in spinal cord tissues 42 days after SPII. In vitro, astrocytes (AST) and BV2 cells were transfected TREM siRNA or the negative control (NC) siRNA to knockdown (KD) TREM1 expressions, followed by lipopolysaccharide (LPS) stimulation to verify the role od TREM1 in modulating SPI. The results suggested that TREM1 was highly expressed in the spinal cord tissues of WT mice after SCI. TREM1(KO) mice exhibited improved locomotor function, mechanical and thermal hypersensitivity in the hindpaws after SCI. In addition, peripheral nerve injury-related biomarkers were down-regulated by TREM1(KO) in SCI mice. TREM1(KO) increased NeuN-stained cells, and decreased GFAP and Iba-1 expressions in spinal cord tissues of mice after SCI. TREM1(KO) mice showed reduced expressions of inflammation-related regulators in the injured spinal cord. Further, toll like receptors (TLR-2, -3, -4, and -9), p-I kappa B alpha and pnuclear factor-kappa B (NF-kappa B) protein expression levels were markedly decreased by TREM1(KO) in mice after SCI injury. Moreover, TREM-deficiency suppressed oxidative stress markers, while enhanced anti-oxidants, such as superoxide dismutase-1 (SOD1), NAD(P) H: quinone oxidoreductase-1 (NQO-1), heme oxygenase-1 (HO-1) and nuclear factor E2-related factor 2 (Nrf2) in the

关键词： Leiomyomas   Leiomyosarcomas   Sarcomas   Uterus   Mesenchymal tumours   MS-HRM   ABERRANT DNA METHYLATION   PROMOTER METHYLATION   MATRIX METALLOPROTEINASES   DOWN-REGULATION   NECROSIS-FACTOR   CANCER   EXPRESSION   LEIOMYOMA   DIAGNOSIS   RECEPTOR  

摘要： Mesenchymal tumours of the corpus uteri comprise common benign lesions - leiomyomas and very rare malignant variants - sarcomas. It can be difficult to distinguish between the particular types of mesenchymal tumours pre-surgically. Primarily, leiomyomas and the very aggressive leiomyosarcomas can be easily mis-diagnosed when using only imaging devices. Therefore, a reliable non-invasive marker for these tumour types would provide greater certitude for patients that the lesion remains benign. Our collection comprises 76 native leiomyomas, an equal number of healthy myometrium samples and 49 FFPE samples of various types of sarcomas. The methylation level was assessed by MS-HRM method and we observed differences in the methylation level between healthy, benign and (semi)malignant tissues in the KLF4 and DLEC1 genes. The mean methylation levels of leiomyomas compared to myometrium and leiomyosarcomas were 70.7% vs. 6.5% vs. 39.6 % (KLF4) and 66.1% vs. 14.08% vs. 37.5% (DLEC1). The ATF3 gene was differentially methylated in leiomyomatous and myometrial tissues with 98.1% compared to 76.6%. The AUC values of the predictive logistic regression model for discrimination between leiomyomas and leiomyosarcomas based on methylation levels were 0.7829 (KLF4) and 0.7719 (DLEC1). Finally, our results suggest that there should be distinct models for the methylation events in benign leiomyomas and sarcomas, and that the KLF4 and DLEC1 genes can be considered potential methylation biomarkers for uterine leiomyomas.

关键词： DUSP1   缺氧   RAW264.7   炎症反应   ATF3  

摘要： 研究背景:高原病(high altitude disease,HAD)是由高原低压缺氧引起的一种高原特发性疾病,根据发病急缓分为急性高原病和慢性高原病两大类。近年来的研究显示,缺氧诱导的炎症反应参与高原病的发生发展,缺氧引起的炎性血管反应是急性高原病的重要机制,而缺氧诱导的炎性增生则是慢性高原病的重要机制。巨噬细胞是一种重要的固有免疫细胞,广泛存在于机体不同的器官组织中,执行多种不同的功能,包括对抗入侵的病原体和肿瘤细胞、协调伤口愈合、参与获得性免疫应答中的抗原提呈等。许多巨噬细胞参与的病理过程(如炎症、伤口愈合、动脉粥样硬化和肿瘤)也都以缺氧为特征。巨噬细胞对缺氧十分敏感,被激活的巨噬细胞可通过表达和分泌某些炎症细胞因子和趋化因子,活化和招募其它炎症细胞,从而参与缺氧引起的组织和机体损伤或重塑。研究显示,缺氧诱导的巨噬细胞炎症反应与高原病的发生发展密切相关。因此,深入认识缺氧诱导的巨噬细胞炎症反应及其调控机制,对于进一步阐明高原病的发病机制和研发防治药物具有重要意义。目前为止,缺氧诱导的巨噬细胞炎症反应调控的具体机制仍不完全清楚。双特异性磷酸酶1(Dual specificity phosphatase 1,DUSP1),也被称作丝裂素活化蛋白激酶磷酸酶1(Mitogen-activated Protein Kinase Phosphatase-1,MKP-1),是DUSP家族中最早被鉴定并且也是其中最重要的成员。DUSP1主要催化细胞内已激活的丝裂原活化蛋白激酶(Mitogen-activated protein kinases,MAPKs)家族成员(p38、JNK与ERK)中特异性基序TXY磷酸基团的水解,从而抑制它们的活性,进而阻断其下游相关生物学反应。Dusp1基因最初是作为在培养的小鼠细胞G0/G1转化过程中表达的一组基因之一而被鉴定的,后来的研究发现,多种应激因素如紫外线、病原体蛋白、缺氧等可以诱导DUSP1表达上调。本研究室前期对平原人急进5300m高原前后全血转录组学的研究结果显示,进入高原后DUSP1的转录水平表达较进入高原前明显升高。关于进入高原后DUSP1表达升高在高原病发生发展中的生物学意义尚并不清楚。鉴于DUSP1在负调控TLR配体诱导的巨噬细胞炎症反应中的重要作用及缺氧诱导的巨噬细胞炎症反应在高原病发生发展中的重要作用,DUSP1可能通过调控缺氧诱导的巨噬细胞炎症反应从而参与到高原病发生发展的调节中。目前关于缺氧引起DUSP1表达升高的机制以及DUSP1是否参与调控缺氧诱导的巨噬细胞炎症反应尚不清楚。采用生物信息学分析的结果显示,活化转录因子3(Activating transcription factor 3,ATF3)可能是调节Dusp1表达的关键分子。因此,我们推测缺氧巨噬细胞可能通过转录因子ATF3上调DUSP1的表达,进而调节缺氧RAW264.7巨噬细胞中部分炎症相关细胞因子的表达,从而防止自身过度炎症免疫反应。本研究使用炎症反应研究中广泛使用的小鼠RAW264.7巨噬细胞建立缺氧巨噬细胞模型,初步探讨DUSP1在缺氧巨噬细胞中的表达机制及其在缺氧诱导的巨噬细胞炎症免疫反应调控中的作用,旨在为高原缺氧损伤的发病机制及防治提供新的思路及部分理论和实验依据。方法:以小鼠RAW264.7巨噬细胞作为研究模型。根据不同的实验目的,分为常氧(21%O)组、缺氧(1%O)组;缺氧+干扰序列对照组(si-C)、缺氧+siRNA组。缺氧组细胞置于缺氧工作站(1%O)中培养,常氧(21%O)组则置于普通培养箱中培养。采用实时荧光定量PCR(Quantitative Real-time PCR,qRT-PCR)、蛋白质印迹法(Western blot,WB)检测缺氧(1%O2)处理不同时间RAW264.7巨噬细胞中DUSP1和ATF3的mRNA和蛋白表达水平。采用qRT-PCR和酶联免疫吸附测定(Enzyme linked immunosorbent assay,ELISA)检测缺氧(1%O)处理不同时间RAW264.7巨噬细胞中炎症相关细胞因子IL-1β、IL-10和TNF-α的mRNA和分泌水平。采用RNA干扰技术干扰Dusp1表达,采用qRT-PCR、WB检测干扰效果;采用qRT-PCR和ELISA检测转染si-Dusp1后缺氧(1%O)处理24h RAW264.7巨噬细胞中IL-1β、IL-10和TNF-α的mRNA和分泌水平。采用RNA干扰技术干扰Atf3表达,采用qRT-PCR、WB检测干扰效果;采用qRT-PCR和WB检测转染si-Atf3后缺氧(1%O)处理24h RAW264.7巨噬细胞中DUSP1的mRNA和蛋白表达水平。采用qRT-PCR和ELISA检测转染si-Atf3后缺氧(1%O

关键词： 黄韧带骨化   ncRNA   成骨细胞分化   miR-342-3p   ATF3  

摘要： 已有研究表明非编码RNA可参与多种生理病理过程,其在疾病的发生发展中发挥重要作用。黄韧带骨化症及骨质疏松症是常见的慢性骨科疾病,如不能得到及时的诊断和治疗,将严重影响患者的生存质量。目前,鲜有报道非编码RNA在黄韧带骨化症或骨质疏松症中的功能及机制。本研究旨在通过基因芯片或测序筛选出骨化黄韧带组织(Ossification of ligamentum flavum,OLF)中显著差异表达的m RNA、lnc RNA、mi RNA及circ RNA,并对差异RNA进行关联分析及功能探究;同时明确mi R-342-3p在成骨分化中的功能及机制,为黄韧带骨化和骨质疏松症的诊断和治疗提供新思路。方法:1.标本采集:收集术中取出的新鲜骨化的黄韧带组织和正常黄韧带组织。用液氮研磨法快速提取组织样本RNA,并通过RNA电泳和2100质量检测法进行检测。从中分别选4个合格的正常黄韧带组织和4个合格的骨化黄韧带组织的RNA进一步实验。2.筛选OLF中差异表达的m RNA:通过基因芯片分析,OLF与正常黄韧带组织(ligamentum flavum,LF)相比,筛选出差异倍数>2,p<0.05的差异m RNAs。随机挑选10个m RNAs在扩大样本中进行q PCR检测表达差异,确证芯片结果可信。进一步做差异m RNAs的GO和KEGG分析,确证这些差异m RNAs是否参与成骨分化。3.筛选OLF中差异表达的lnc RNA:通过基因芯片分析,OLF与LF相比,筛选出差异倍数>2,p<0.05的差异lnc RNAs。随机挑选10个lnc RNAs在扩大样本中进行q PCR检测表达差异,确证芯片结果可信。选择两个上调的lnc RNAs,在h MSCs向成骨分化过程中,分别敲低lnc RNA后,通过q PCR检测促成骨分化相关基因表达量的改变,并进行ALP染色,确证差异lnc RNAs在细胞成骨分化中的作用。在m RNAs芯片结果中挑选10个已知的与骨化或成骨分化相关的差异m RNAs,联合m RNAs和lnc RNAs芯片结果,筛选出与上述m RNAs共表达的差异lnc RNAs,构建共表达(conding-non-coding,CNC)网。4.筛选OLF中差异表达的mi RNA:通过基因测序技术,OLF与LF相比,筛选出差异倍数>2,p<0.05的差异mi RNAs。随机挑选10个mi RNAs在扩大样本中进行q PCR检测表达差异,确证芯片结果可信。选定一个下调的mi RNA,在h MSCs向成骨分化过程中过表达,通过q PCR检测促成骨分化相关基因的表达变化,同时进行ALP染色,确证差异mi RNA在细胞成骨分化中的作用。通过Target Scan,mi RBase和mi Randa数据库,预测差异mi RNAs的靶基因;同时与m RNAs芯片结果中差异m RNAs取交集,进一步再筛选出与mi RNAs负性差异表达关联的m RNAs。进行上述筛选出的m RNAs的GO和KEGG分析,确证其是否与骨化相关。5.筛选OLF中差异表达的circ RNA:通过基因芯片技术,OLF与LF相比,筛选出差异倍数>2,p<0.05的差异circ RNAs。随机挑选10个circ RNAs在扩大样本中进行q PCR检测表达差异,确证芯片结果可信。选择一个上调的circ RNA进行功能验证。在h MSCs向成骨分化过程中,敲低选定的circ RNA后,通过q PCR检测ALP、Col1α1、Bglap及RUNX2的表达量变化,并进行ALP染色,确证差异circ RNA在细胞成骨分化中的作用。软件预测验证的lnc RNAs、circ RNA及mi RNA是否存在关联,以此进一步构建ce RNA调节网。6.确定成骨分化过程中mi R-342-3p的表达水平:在OLF和正常黄韧带样本中,健康体检者、OLF及骨质疏松患者的血标本中,骨质疏松模型小鼠股骨组织中及细胞成骨分化诱导过程中,通过q PCR检测ALP、OCN及mi R-342-3p的水平。7.确定mi R-342-3p在细胞成骨分化中的功能:分别用mi R-342-3p抑制剂(antagomir-342-3p)或mi R-342-3p激动剂(agomir-342-3p)转染原代人骨髓间充质干细胞h MSCs,q PCR确保mi R-342-3p的干扰和过表达效果,进一步成骨诱导培养3天或6天后,提取RNA和蛋白质,通过q PCR和Western Blot检测促成骨分化相关基因的表达;诱导6天时,通过ALP染色和活性检测测定ALP的沉积和活性,茜素红染色检测钙结节的形成。同时检测mi R-342-3p在小鼠前成骨细胞MC3T3-E1向成骨细胞分化过程中的作用。8.确定mi R-342-3p的作用机制:通过mi RWal

关键词： 脂蛋白脂肪酶   藻蓝蛋白   miR-10a-5p   TAK1   JNK   ATF3  

摘要： [背景与目的]动脉粥样硬化(As)是由脂质代谢紊乱等多种因素引起的一种血管退行性病变,严重危害人类健康。在As众多的发病机理中,巨噬细胞源性泡沫细胞的形成构成其核心环节。因此,减少巨噬细胞源性泡沫细胞形成对As的防治具有重要意义。以往研究表明,脂蛋白脂酶(LPL)是水解血浆甘油三酯的关键限速酶,对降低血浆甘油三酯水平至关重要。然而,LPL在巨噬细胞中却通过介导细胞内脂质蓄积促进泡沫细胞形成,从而发挥促As的作用。探索调控LPL表达的作用机制,减少巨噬细胞脂质蓄积,对于防治As具有重要意义。藻蓝蛋白(PC)是一种存在于藻类中的色素蛋白,在螺旋藻中的含量约为10%0%,常温下结构稳定。研究表明,PC在抗氧化、抗肿瘤、免疫应答等方面发挥着多种生物学功能,但其是否通过减少巨噬细胞脂质蓄积从而影响泡沫细胞形成的机制尚未阐明。丝裂原活化蛋白激酶激酶激酶7(TAK1),能够调节细胞的增殖与凋亡,介导多种促炎症和促存活信号通路的激活,参与As的病理进程。应激活化蛋白激酶(JNK)是位于TAK1下游的因子,TAK1表达升高可增加磷酸化JNK水平,从而引起JNK下游因子的激活或抑制。转录激活因子3(ATF3),是ATF/环磷腺苷效应元件结合蛋白转录因子家族的成员,位于JNK下游,它是富含甘油三酯的脂蛋白脂解产物的关键反应基因,能够诱导促炎因子聚集,促进As的发生。然而,TAK1/JNK/ATF3信号途径是否参与PC调控巨噬细胞LPL表达及脂质蓄积的机制尚不清楚。miR-10a-5p是新近发现的一个RNA分子,与肿瘤的发生、炎症反应密切相关。研究发现,miR-10a-5p能够靶向结合TAK1,从而增加As斑块的面积,加速As的发生。但miR-10a-5p是否参与PC调控巨噬细胞LPL表达及脂质蓄积的机制尚不明确。因此,本研究的目的是从脂质代谢的角度,探究PC对巨噬细胞LPL表达及脂质蓄积的影响机制。[方法]THP-1细胞置于10%胎牛血清(PBS)的RPMI 1640培养基(含10U/mL青霉素和10U/mL链霉素)中培养,将细胞培养箱温度保持在37℃,同时保证箱内5%的CO浓度。用160nmol/L的佛波醇(PMA)孵育THP-1细胞48小时,促进其分化,转变为巨噬细胞,50μg/ml的氧化低密度脂蛋白(ox-LDL)无血清培养基处理细胞。首先,PC(5、10、20μg/ml)或PBS孵育巨噬细胞6、12、24小时,然后用RT-PCR和Western Blot检测LPL mRNA及表达,LPL活性比色法定量检测试剂盒检测LPL活性,高效液相色谱(HPLC)用于检测细胞内脂质含量变化情况;染色质免疫共沉淀(ChIP)和荧光素酶报告基因(Luciferase)分别检测PC对转录因子ATF3与LPL启动子区结合以及LPL启动子活性的影响,RT-PCR和Western Blot分别检测PC对ATF3 mRNA及表达,LPL mRNA及表达的影响;接着,使用TAK1过表达质粒,JNK激活剂茴香霉素和ATF3过表达质粒处理后,RT-PCR和Western Blot分别检测PC对TAK1 mRNA及表达、JNK及其磷酸化水平、ATF3 mRNA及表达,LPL mRNA及表达的影响,验证PC是否通过TAK1/JNK/ATF3信号通路影响LPL的表达。最后,利用生物信息学分析手段预测并比对不同物种间miR-10a-5p的序列、保守性及其靶标基因,以此为基础确定miR-10a-5p与TAK1存在结合位点,借助MicroRNA靶标预测网站对两者的结合自由能进行评分。荧光素酶报告基因检测miR-10a-5p与TAK1 3’UTR靶向结合情况,miR-10a-5p抑制剂转染巨噬细胞24小时,同时加入PC进行处理,RT-PCR和Western Blot检测相关基因及蛋白的表达情况。[结果]RT-PCR,Western Blot和HPLC检测发现,PC处理的巨噬细胞中LPL mRNA及表达、总胆固醇、游离胆固醇,胆固醇酯的水平呈浓度和时间依赖性显著降低;通过生物信息学预测分析发现转录因子ATF3与LPL的启动子之间可能存在结合位点;荧光素酶报告基因和ChIP的结果表明,转录激活因子ATF3能够增强LPL启动子的活性,PC明显抑制ATF3与LPL启动子的结合;RT-PCR和Western Blot检测发现,PC减少ATF3 mRNA及表达并下调LPL mRNA及表达,但当过表达ATF3后,能够逆转PC对LPL的抑制作用,表明ATF3是参与调控LPL的关键因子。接下来检测PC对JNK的影响,结果发现PC能够抑制JNK的激活,并且在使用JNK激活剂茴香霉素处理后,恢复了ATF3与LPL mRNA及表达;JNK是MAPK信号通路的另一亚类,其中TAK1是JNK的上游,进一步检测PC对

关键词： ATF3   ferroptosis   SLC7A11   system Xc~-   metabolic stress   erastin   p53  

摘要： OBJECTIVE The amino acid antiporter system Xc;is important for the synthesis of glutathione（GSH） that functions to prevent lipid peroxidation and protect cells from nonapoptotic, iron-dependent death（ie, ferroptosis）. Inhibition of system Xc;activity by small molecules（eg, erastin） can cause a decrease in the intracellular GSH level, leading to ferroptotic cell death. While the activity of system Xc;is mainly determined by the expression level of its subunit encoded by the gene SLC7A11, the mechanism by which system Xc;is regulated during ferroptosis remains largely unknown. The goal of this study is to determine whether ATF3, a common stress sensor, can regulate system Xc;activity and promote ferroptosis. METHODS Ferroptosis was evaluated by cell viability assays and confirmed by treating cells with ferrostatin-1. Lipid peroxidation was measured by flow cytometry after cell staining with BODIPY 581/591C11. The activity of system Xc;was measured by glutamate release and GSH assay. The binding of ATF3 to the SLC7A11 promoter was determined by chromatin immunoprecipitation and DNA affinity precipitation assays. The activity of SLC7A11 promoter or mutated promoters was measured by dual luciferase reporter assays. RESULTS Overexpression of ATF3 in various cancer cells（eg, HT1080） promoted lipid peroxidation and ferroptosis induced by erastin and other ferroptosis inducers（eg, RSL3）. Conversely, knockout of ATF3 expression blocked the accumulation of lipid peroxides and prevented cells from undergoing ferroptosis. ATF3 appeared to promote ferroptosis by inhibiting system Xc;,as ATF3 expression decreased, while ATF3 knockout increased, the amount of released glutamate and the intracellular GSH level. Moreover, bypassing system Xc;by treating cells with 2-mercaptoethanol（2-ME） or N-acetylcysteine（NAC） could alleviate the effects of ATF3 on ferroptosis. Mechanistically, ATF3 strongly bound to the SLC7 A11 promoter and repressedits activity. Mutating the putative ATF3-bindin

关键词： Deoxynivalenol   Cell cycle   ATF3   EGR1   Histone acetylation   GENE-EXPRESSION   T-2 TOXIN   ATF3   EXPOSURE   TRICHOTHECENES   MODULATION   REDUCTION   VOMITOXIN   APOPTOSIS   UPDATE  

摘要： Deoxynivalenol (DON) is a type B trichothecene mycotoxin that exerts multiple toxic effects on plants, animals and humans. Several reports have shown that DON leads to G2/M cell cycle arrest. However, its molecular mechanism is still unclear. In this study, we showed that DON induced strong G2/M cell cycle arrest in HepG2 cells, and the cell cycle-inhibitory protein p21 was highly upregulated by DON. Further analysis showed that the cell cycle regulating gene EGR1 was highly induced by DON and that EGR1 knockdown abolished the upregulation of p21 and G2/M cell cycle arrest. Furthermore, we showed that the induction of EGR1 was regulated by the stressresponsive transcription factor ATF3. ATF3 Delta Zip2a/2b, which is a DNA binding domain truncated isoform of ATF3, was upregulated by DON. ATF3 knockdown weakened the expression induction of EGR1 and G2/M cell cycle arrest by DON. Moreover, the upregulation of ATF3 Delta Zip2a/2 highly depended on the enhanced presence of histones H3K9ac and H3K27ac. H3K9ac and H3K27ac were enriched at the promoter region of ATF3 following the DON treatment, and the knocking down of the genes responsible for H3K9ac and H3K27ac abolished the upregulation of ATF3 by DON. In summary, we found that DON induced G2/M cell cycle arrest by sequentially inducing the expression of ATF3 Delta Zip2a/2b, EGR1 and p21, and EGR1 played an essential role in this process, which is a novel molecular mechanism of cell cycle arrest by DON and is important for understanding its toxicology.