Atherosclerosis Research Unit, Center for Molecular Medicine, Department of Medicine, Karolinska Institutet, Stockholm, Sweden.
J Mol Med (Berl). 2013 Jan;91(1):129-39. doi: 10.1007/s00109-012-0942-8. Epub 2012 Aug 18.
Individuals with bicuspid aortic valve (BAV) are at significantly higher risk of developing serious aortic complications than individuals with tricuspid aortic valves (TAV). Studies have indicated an altered aortic blood flow in patients with BAV; however, the extent to which altered flow influences the pathological state of BAV aorta is unclear. In the present study, we dissected flow-mediated aortic gene expression in patients undergoing elective open heart surgery. A large collection of public microarray data sets were firstly screened for consistent co-expression with five well-characterized flow-regulated genes (query genes). Genes with co-expression probability of >0.5 were selected and further analysed in expression profiles (127 arrays) from ascending aorta of BAV and TAV patients. Forty-four genes satisfied two filtering criteria: a significant correlation with one or more of the query genes (R > 0.40) and differential expression between patients with BAV and TAV. No gene fulfilled the criteria in mammary artery (88 arrays), an artery not in direct contact with the valve. Fifty-five percent of the genes significantly altered between BAV and TAV patients showed differential expression between two identified flow regions in the rat aorta. A large proportion of the identified genes were related to angiogenesis and/or wound healing, with pro-angiogenesis genes downregulated and inhibitory genes upregulated in patients with BAV. Moreover, differential expression of ZFP36, GRP116 and PKD2 was confirmed using immunohistochemistry. Implementing a new strategy, we have demonstrated an angiostatic gene expression signature in patients with BAV, indicating impaired wound healing in these patients, potentially involved in BAV-associated aortopathy.
二叶式主动脉瓣(BAV)个体发生严重主动脉并发症的风险明显高于三叶式主动脉瓣(TAV)个体。研究表明,BAV 患者的主动脉血流发生改变;然而,血流改变对 BAV 主动脉病理状态的影响程度尚不清楚。在本研究中,我们对接受择期心脏直视手术的患者进行了血流介导的主动脉基因表达分析。首先筛选了大量公共微阵列数据集,以寻找与五个特征明确的流量调节基因(查询基因)一致的共表达。选择共表达概率>0.5 的基因,并在 BAV 和 TAV 患者升主动脉的表达谱(127 个数组)中进一步分析。44 个基因符合两个过滤标准:与一个或多个查询基因呈显著相关(R>0.40),并且在 BAV 和 TAV 患者之间存在差异表达。在不直接与瓣膜接触的乳内动脉(88 个数组)中没有基因符合该标准。在 BAV 和 TAV 患者之间显著改变的 44 个基因中,有 55%在大鼠主动脉的两个确定的血流区域之间表现出差异表达。鉴定出的基因中有很大一部分与血管生成和/或伤口愈合有关,BAV 患者的促血管生成基因下调,抑制性基因上调。此外,使用免疫组织化学证实了 ZFP36、GRP116 和 PKD2 的差异表达。通过实施一种新策略,我们在 BAV 患者中展示了一个血管生成抑制基因表达谱,表明这些患者的伤口愈合受损,这可能与 BAV 相关的主动脉病变有关。