Ben-Shoshan Jeremy, Keren Gad, George Jacob
The Department of Cardiology, Tel Aviv Sourasky Medical Center.
Harefuah. 2006 May;145(5):362-6, 397.
Accumulating evidence suggests that postnatal bone marrow is a source of cells that can participate in postnatal neovascularization and vascular homeostasis. Among these cells, a scarce population of endothelial progenitor cells (EPCs) have the capacity to migrate to the peripheral circulation, proliferate and differentiate into mature endothelial cells in response to stimulating signals emanating from vascular injuries or during tumor growth. Questions persist, however, regarding the precise panel of cell surface markers that defined EPCs, as well as the different mechanisms stimulating or inhibiting their mobilization and differentiation. In the last decade, EPCs number and function have been correlated with risk factors for cardiovascular and peripheral vascular diseases. The authors review experimental results obtained from both animal studies and recent clinical trials, which point to the importance of EPCs potential as diagnostic markers and therapeutic tools in ischemic diseases. Furthermore, the article discusses the risk of potentially harmful side effects of altered EPCs number and functional properties, a critical barrier to overcome while bringing progenitor cell therapy to the clinical arena.
越来越多的证据表明,出生后的骨髓是能够参与出生后新血管形成和血管稳态维持的细胞来源。在这些细胞中,数量稀少的内皮祖细胞(EPCs)有能力迁移至外周循环,增殖并在来自血管损伤或肿瘤生长的刺激信号作用下分化为成熟内皮细胞。然而,关于定义EPCs的精确细胞表面标志物组合,以及刺激或抑制其动员和分化的不同机制,仍存在疑问。在过去十年中,EPCs的数量和功能已与心血管和外周血管疾病的危险因素相关联。作者回顾了来自动物研究和近期临床试验的实验结果,这些结果表明EPCs作为缺血性疾病诊断标志物和治疗工具的潜力的重要性。此外,本文还讨论了EPCs数量和功能特性改变可能产生有害副作用的风险,这是将祖细胞疗法引入临床领域时需要克服的关键障碍。