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首页> 外文期刊>Modern Pathology >Gene expression and clonality analysis of the androgen receptor and phosphoglycerate kinase genes in polygonal cells and cuboidal cells in so-called pulmonary sclerosing hemangioma
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Gene expression and clonality analysis of the androgen receptor and phosphoglycerate kinase genes in polygonal cells and cuboidal cells in so-called pulmonary sclerosing hemangioma

机译:雄激素受体和磷酸甘油糖激酶基因在多边形细胞中的基因表达和克隆性分析及所谓的肺结核血管瘤中的立方体细胞

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The histogenesis of polygonal cells and cuboidal cells in so-called pulmonary sclerosing hemangioma remains unclear. To understand their histogenesis, polygonal and cuboidal cells were obtained from pulmonary sclerosing hemangioma tissue using a laser capture microdissection technique. Genomic DNA and total RNA were extracted and mRNA levels of cytokeratin, epithelial membrane antigen, vimentin, surfactant protein B, thyroid transcription factor-1, synaptophysin, and chromogranin-A were analyzed by RT-PCR. DNA was digested with the methylation-sensitive enzymes HhaI or HpaII, followed by nested PCR of the androgen receptor and phosphoglycerate kinase genes. Samples with polymorphisms were identified and a clonality analysis was performed. The cytokeratin, epithelial membrane antigen, and surfactant protein B genes were clearly expressed in cuboidal cells, while the vimentin and synaptophysin genes were clearly expressed and the epithelial membrane antigen gene was weakly expressed in polygonal cells. Thyroid transcription factor-1 was expressed in both cell types, while neither cell type expressed chromogranin-A. Clonality analysis showed the same loss of allele in both cell types (clonality ratio=0) or an unbalanced methylation pattern (clonality ratio <0.25). Polygonal and cuboidal cells in pulmonary sclerosing hemangioma exhibited a uniform pattern of monoclonality, indicating that both cell types are highly likely to originate from a common precursor. The differences in their morphological phenotype might result from their different mature status.
机译:多边形细胞的组织和立方体细胞中所谓的肺硬化血管瘤的组织诱发仍不清楚。为了了解它们的组织发生,使用激光捕获微量碎裂技术从肺硬化血管瘤组织获得多边形和立方体细胞。通过RT-PCR提取基因组DNA和总RNA,细胞角蛋白,上皮膜抗原,Vimentin,表面活性剂蛋白B,甲状腺转录因子-1,Sypaptophysin和Chromogranin-A的mRNA水平。用甲基化敏感酶Hai或HPAII消化DNA,然后嵌套PCR的雄激素受体和磷酸甘油糖激酶基因。鉴定具有多态性的样品并进行克隆性分析。在立方体细胞中清楚地表达了细胞角蛋白,上皮膜抗原和表面活性剂蛋白B基因,而显然表达了平方和突触蛋白基因,并且上皮膜抗原基因在多边形细胞中弱。在两种细胞类型中表达甲状腺转录因子-1,而既不表达细胞型表达染色体素-A。克隆性分析表明,在细胞类型(克隆性比率= 0)或不平衡甲基化模式(克隆性比<0.25)中相同的等位基因丧失。肺硬化血管瘤中的多边形和立方体细胞表现出均匀的单蛋白石模式,表明两种细胞类型很可能来自常见前体。它们的形态表型的差异可能是由于其不同的成熟地位。

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