Tanriover Gamze, Sozen Berna, Seker Askin, Kilic Turker, Gunel Murat, Demir Necdet
Department of Histology and Embryology, Akdeniz University, School of Medicine, Antalya 07070, Turkey.
Clin Neurol Neurosurg. 2013 Apr;115(4):438-44. doi: 10.1016/j.clineuro.2012.06.023. Epub 2012 Jul 7.
Investigation of the structure of vascular malformations highlights the pathogenic mechanisms underlying their clinical behavior. One of the vascular malformations is called cerebral cavernous malformation (CCM). However, the ultrastructural features of the vascular malformations are not defined in detail.
We aimed to investigate the ultrastructural features of CCMs using transmission (TEM), scanning (SEM) electron microscopy, and also immunohistochemistry methods with antibodies against CCM proteins such as CCM2 and CCM3. CCM tissues (n=6) microsurgically excised from patients for conventional indications.
CCM2 and CCM3 were strongly detected in the vascular endothelium. However, there was a very weak immunostaining in stroma. SEM observations revealed that there were ruptures and damages in the luminal endothelium, possibly due to the damage of intercellular junctions. TEM observations also showed a few ruptures and detachments between the endothelium and basal lamina as observed with partially damages and disconnections. The architecture of pericytes showed protrusions and shrinkages. Our results suggest that the thin vessel walls of CCMs were lacking of subendothelial support and intact basal lamina underlying the endothelial cells.
This study is so far the first study attempting to show human CCM lesions with SEM. We believe that an understanding of the ultrastructural features of these lesions by light and electron microscopy techniques would help to understand the pathology of these diseases.
对血管畸形结构的研究突出了其临床行为背后的致病机制。其中一种血管畸形称为脑海绵状畸形(CCM)。然而,血管畸形的超微结构特征尚未得到详细界定。
我们旨在使用透射电子显微镜(TEM)、扫描电子显微镜(SEM)以及针对CCM蛋白(如CCM2和CCM3)的抗体进行免疫组织化学方法来研究CCM的超微结构特征。CCM组织(n = 6)是从患者身上通过显微手术切除的,用于常规适应症。
在血管内皮中强烈检测到CCM2和CCM3。然而,在基质中免疫染色非常弱。SEM观察显示管腔内内皮存在破裂和损伤,可能是由于细胞间连接的破坏。TEM观察还显示,在内皮细胞与基膜之间存在一些破裂和分离,观察到部分损伤和断开。周细胞的结构显示出突起和收缩。我们的结果表明,CCM的薄壁血管缺乏内皮下支持以及内皮细胞下方完整的基膜。
本研究是迄今为止首次尝试用SEM展示人类CCM病变的研究。我们相信,通过光学和电子显微镜技术了解这些病变的超微结构特征将有助于理解这些疾病的病理学。