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Gene profile in the spleen under massive partial hepatectomy using complementary DNA microarray and pathway analysis

机译:使用互补DNA微阵列和通路分析的大部分肝切除术后脾脏的基因谱

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Background and Aim: In general, the spleen is one of the abdominal organs connected by the portal system, and a splenectomy improves hepatic functions in the settings of partial hepatectomy (Hx) for portal hypertensive cases or living donor liver transplantation with excessive portal vein flow. Those precise mechanisms remain still unclear; therefore, we investigated the DNA expression profile in the spleen after 90% Hx in rats using complementary DNA microarray and pathway analysis. Methods: Messenger RNAs (mRNAs) were prepared from three rat spleens at each time point (0, 3, and 6h after 90% Hx). Using the gene chip, mRNA was hybridized to Affymetrix GeneChip Rat Genome 230 2.0 Array (Affymetrix?) and pathway analysis was done with Ingenuity Pathway Analysis (IPA?). Results: We determined the 3-h or 6-h/0-h ratio to assess the influence of Hx, and cut-off values were set at more than 2.0-fold or less than 1/2 (0.5)-fold. Chemokine activity-related genes including Cxcl1 (GRO1) and Cxcl2 (MIP-2) related pathway were upregulated in the spleen. Also, immediate early response genes including early growth response-1 (EGR1), FBJ murine osteosarcoma (FOS) and activating transcription factor 3 (ATF3) related pathway were upregulated in the spleen. Conclusions: We concluded that in the spleen the expression of numerous inflammatory-related genes would occur after 90% Hx. The spleen could take a harmful role and provide a negative impact during post Hx phase due to the induction of chemokine and transcription factors including GRO1 and EGR1.
机译:背景与目的:脾脏通常是门静脉系统连接的腹部器官之一,对于门静脉高压病例或活体供体肝移植,门静脉血流量过多,脾切除术可改善部分肝切除(Hx)的肝功能。 。这些确切的机制仍然不清楚。因此,我们使用互补DNA微阵列和通路分析研究了90%Hx后大鼠脾脏中的DNA表达谱。方法:在每个时间点(90%Hx后的0、3和6h)从三个大鼠脾脏制备Messenger RNA(mRNA)。使用该基因芯片,将mRNA与Affymetrix GeneChip Rat Genome 230 2.0 Array(Affymetrix?)杂交,并通过“独创性途径分析”(IPA?)进行途径分析。结果:我们确定3小时或6小时/ 0小时的比率来评估Hx的影响,并且临界值设置为大于2.0倍或小于1/2(0.5)倍。脾脏中与Cxcl1(GRO1)和Cxcl2(MIP-2)相关途径相关的趋化因子活性相关基因被上调。此外,脾脏中的早期早期反应基因,包括早期生长反应-1(EGR1),FBJ鼠骨肉瘤(FOS)和激活转录因子3(ATF3)相关途径也被上调。结论:我们得出结论,在90%Hx后,脾脏中会出现许多炎症相关基因的表达。由于诱导趋化因子和转录因子(包括GRO1和EGR1),脾脏可能在Hx后阶段起有害作用并产生负面影响。

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