Arismendi-Morillo Gabriel, Castellano Alan
Biological Researches Institute, Faculty of Medicine, University of the Zulia, Apartado 526, Maracaibo, 4003-A, Venezuela.
J Neurooncol. 2005 Jul;73(3):211-7. doi: 10.1007/s11060-004-5674-3.
The development of peritumoral edema is thought to be due to extravasation of plasma water and macromolecules through a defective blood-brain barrier (BBB), but the exact mechanism by which occurs is poorly understood. The aim of this study was analyze at submicroscopic level the morphological changes in both micro-blood vessels and vascular microenvironment of astrocytic tumors in an attempt of understanding the pathological aspects that may help in the future researches for the design of future therapeutic strategies. Biopsies of 25 patients with pathological diagnosis of astrocytic tumors were examined with the transmission electron microscope. Both open and close tight junctions were observed in the micro-blood vessels, inclusive in a same tumor. Cytoskeletal disorganization associated with disintegrated perijunctional actin filaments were seen. The paracellular space showed enlargement and commonly occupied by fluid proteinaceous, endothelial cells display oncotic and ischemic changes, basal lamina reveals enlargement, edema, vacuolization and collagen fibers disposed in irregular array. Pericytes exhibited edema and phagocytoced material, astrocytic perivascular-feet showed signs of oncosis and necrosis, co-option vessels totally surrounding by neoplastic cells also were seen. The ultrastructural abnormalities observed in both junctional complexes and vascular microenvironment suggest a multi-factorial pathobiology process, probably hypoxia intratumoral, calcium overload in endothelial cells, and degradative effects of metalloproteinases over the basal membrane appear as determinant factors that leading to structural modifications of junctional complexes, therefore, treatment with both HIF-1alpha and metalloproteinases inhibitors possibly can contribute with the pharmacological handling of the peritumoral edema associated with astrocytic tumors.
瘤周水肿的发生被认为是由于血浆水和大分子物质通过有缺陷的血脑屏障(BBB)外渗所致,但其确切发生机制尚不清楚。本研究的目的是在亚微观水平分析星形细胞瘤微血管和血管微环境的形态学变化,以试图了解可能有助于未来设计治疗策略的病理方面。对25例经病理诊断为星形细胞瘤的患者活检组织进行透射电子显微镜检查。在微血管中观察到开放和紧密连接,包括在同一肿瘤中。可见细胞骨架紊乱伴连接周肌动蛋白丝解体。细胞旁间隙增大,通常充满液体蛋白质,内皮细胞呈现肿胀和缺血性改变,基底膜显示增大、水肿、空泡化以及胶原纤维排列不规则。周细胞出现水肿并吞噬物质,星形胶质细胞血管周足显示肿胀和坏死迹象,还可见被肿瘤细胞完全包围的共选血管。在连接复合体和血管微环境中观察到的超微结构异常提示了一个多因素的病理生物学过程,可能肿瘤内缺氧、内皮细胞钙超载以及金属蛋白酶对基底膜的降解作用是导致连接复合体结构改变的决定性因素,因此,用HIF-1α和金属蛋白酶抑制剂治疗可能有助于对与星形细胞瘤相关的瘤周水肿进行药物处理。