Chiang Elaine Y, Frenette Paul S
Department of Medicine, Mount Sinai School of Medicine, New York, NY 10029, USA.
Hematol Oncol Clin North Am. 2005 Oct;19(5):771-84, v. doi: 10.1016/j.hoc.2005.08.002.
The vaso-occlusion model has evolved impressively over the past several decades from polymerization-based concepts to a complex, wide-ranging schema that involves multistep, heterogeneous, and interdependent interactions among sickle erythrocytes (SSRBCs), adherent leukocytes, endothelial cells, plasma proteins, and other factors. Endothelial activation, induced directly or indirectly by the proinflammatory behavior of SSRBCs, is the most likely initiating step toward vaso-occlusion. Given the complexity and dynamic relationships of the potential mechanisms leading to vaso-occlusion, further in vivo studies in relevant sickle cell animal models will most likely yield the greatest advances and promote the development of novel, more effective therapeutic strategies.
在过去几十年中,血管闭塞模型已经从基于聚合的概念显著发展为一个复杂、广泛的模式,该模式涉及镰状红细胞(SSRBCs)、黏附白细胞、内皮细胞、血浆蛋白和其他因素之间的多步骤、异质性和相互依存的相互作用。由SSRBCs的促炎行为直接或间接诱导的内皮激活,是血管闭塞最可能的起始步骤。鉴于导致血管闭塞的潜在机制的复杂性和动态关系,在相关镰状细胞动物模型中进行进一步的体内研究很可能会取得最大进展,并促进新型、更有效治疗策略的发展。