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Identification of novel target genes in human lung tissue involved in chronic obstructive pulmonary disease

机译:鉴定慢性阻塞性肺疾病涉及的人肺组织中的新靶基因

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Introduction: As part of a study aimed at illuminating at least some of the complex molecular events taking place in COPD, we screened tissues by means of transcriptome analyses. Materials and methods: Tissues were subjected to transcriptome analysis. Candidate genes were identified and validated by immunohistochemistry. Primary human lung cells were subjected to stimulation with cigarette smoke extract for further validation by real time PCR. Results: Six candidate genes were selected for further investigations: Aquaporin 3 ( AQP3 ), extracellular matrix protein 1 ( ECM1 ), four and a half LIM domain 1 ( FHL1 ), milk fat globule epidermal growth factor 8 ( MFGE8 , lactadherin), phosphodiesterase 4D-interacting protein ( PDE4DIP ), and creatine transporter SLC6A8 . All six proteins were allocated to distinct cell types by immunohistochemistry. Upon stimulation with cigarette smoke extract, human type II pneumocytes showed a dose-dependent down-regulation of MFGE8 , while ECM1 and FHL1 also tended to be down-regulated. Although present, none of the candidates was regulated by cigarette smoke extract in primary human macrophages. Discussion: MFGE8 turned out to be an interesting new candidate gene in COPD deserving further studies.
机译:简介:作为旨在阐明COPD中发生的至少一些复杂分子事件的研究的一部分,我们通过转录组分析筛选了组织。材料和方法:对组织进行转录组分析。通过免疫组织化学鉴定和验证候选基因。用香烟烟雾提取物刺激原代人肺细胞,以通过实时PCR进一步验证。结果:选择了六个候选基因进行进一步研究:水通道蛋白3(AQP3),细胞外基质蛋白1(ECM1),四个半LIM结构域1(FHL1),乳脂球表皮生长因子8(MFGE8,乳粘附素),磷酸二酯酶4D相互作用蛋白(PDE4DIP)和肌酸转运蛋白SLC6A8。通过免疫组织化学将所有六个蛋白质分配给不同的细胞类型。在用香烟烟雾提取物刺激后,人类II型肺细胞显示了MFGE8的剂量依赖性下调,而ECM1和FHL1也趋于下调。尽管存在,但没有候选人受原代人类巨噬细胞中香烟烟雾提取物的调节。讨论:MFGE8成为COPD中有趣的新候选基因,值得进一步研究。

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