Mourino-Alvarez Laura, Iloro Ibon, de la Cuesta Fernando, Azkargorta Mikel, Sastre-Oliva Tamara, Escobes Iraide, Lopez-Almodovar Luis F, Sanchez Pedro L, Urreta Harkaitz, Fernandez-Aviles Francisco, Pinto Angel, Padial Luis R, Akerström Finn, Elortza Felix, Barderas Maria G
Department of Vascular Physiopathology, Hospital Nacional de Parapléjicos, SESCAM, Toledo, Spain.
Proteomics Platform, CIC bioGUNE, CIBERehd, ProteoRed-ISCIII, Bizkaia Science and Technology Park, Derio, Spain.
Sci Rep. 2016 Jun 3;6:27106. doi: 10.1038/srep27106.
Aortic stenosis (AS) is the most common form of valve disease. Once symptoms develop, there is an inexorable deterioration with a poor prognosis; currently there are no therapies capable of modifying disease progression, and aortic valve replacement is the only available treatment. Our goal is to study the progression of calcification by matrix-assisted laser desorption ionization imaging mass spectrometry (MALDI-IMS) and get new insights at molecular level that could help in the understanding of this disease. In this work, we analyzed consecutive slices from aortic valve tissue by MALDI-IMS, to establish the spatial distribution of proteins and peptides directly from the surface of the histological sections. The analysis showed different structures corresponding to regions observed in conventional histology, including large calcification areas and zones rich in collagen and elastic fibers. Peptide extraction from the tissue, followed by liquid chromatography mass spectrometry analysis, provided the identification of collagen VI α-3 and NDRG2 proteins which correlated with the masses obtained by MALDI-IMS and were confirmed by immunohistochemistry. These results highlighted the molecular mechanism implied in AS using MALDI-IMS, a novel technique never used before in this pathology. In addition, we can define specific regions proving a complementary resolution of the molecular histology.
主动脉瓣狭窄(AS)是最常见的瓣膜疾病形式。一旦出现症状,病情就会不可避免地恶化,预后较差;目前尚无能够改变疾病进展的治疗方法,主动脉瓣置换是唯一可用的治疗手段。我们的目标是通过基质辅助激光解吸电离成像质谱(MALDI-IMS)研究钙化的进展,并在分子水平上获得新的见解,以帮助理解这种疾病。在这项工作中,我们通过MALDI-IMS分析了主动脉瓣组织的连续切片,以直接从组织学切片表面确定蛋白质和肽的空间分布。分析显示出与传统组织学中观察到的区域相对应的不同结构,包括大的钙化区域以及富含胶原蛋白和弹性纤维的区域。从组织中提取肽,然后进行液相色谱质谱分析,鉴定出了与MALDI-IMS获得的质量相关的胶原蛋白VIα-3和NDRG2蛋白,并通过免疫组织化学得到了证实。这些结果突出了使用MALDI-IMS研究AS所涉及的分子机制,这是一种此前从未在该病理学中使用过的新技术。此外,我们可以定义特定区域,证明分子组织学具有互补性分辨率。