Division of Cardiology, Department of Medicine, University of Miami, Florida, USA.
Antioxid Redox Signal. 2012 Jan 1;16(1):85-91. doi: 10.1089/ars.2011.4139. Epub 2011 Sep 22.
Maintenance of healthy arteries requires a balance between injuries to the arterial wall and processes of intrinsic arterial repair. Such repair requires the availability of progenitor cells that are local to the wall itself. Progenitor cells from distant reservoirs like the bone marrow may also contribute to repair. Arterial repair seems to degrade over a lifetime, particularly with risk factors such as smoking and diabetes. Hence, a potential preventive/therapeutic strategy for atherosclerosis could be transfusion of competent bone marrow cells (BMCs) to restore effective repair in the face of arterial injury and depleted endogenous repair reservoirs. The challenge with this strategy has been the reliable collection and/or generation of BMCs that support arterial repair. In this study, we describe a set of experiments to elucidate a method of culturing BMCs that robustly retards atherosclerosis development in apolipoprotein E knockout mice. Identifying such a method would represent an important step in developing cell-based treatments for patients with proclivity for developing atherosclerosis.
维持健康的动脉需要平衡动脉壁的损伤和内在动脉修复过程。这种修复需要可用的祖细胞,这些祖细胞位于壁本身的附近。来自骨髓等远处储库的祖细胞也可能有助于修复。动脉修复似乎会随着时间的推移而退化,特别是在吸烟和糖尿病等危险因素的情况下。因此,针对动脉粥样硬化的潜在预防/治疗策略可能是输注功能齐全的骨髓细胞(BMC),以在面对动脉损伤和内源性修复储备耗尽时恢复有效的修复。该策略的挑战一直是可靠地收集和/或生成支持动脉修复的 BMC。在这项研究中,我们描述了一组实验,以阐明一种培养 BMC 的方法,该方法可有效地延缓载脂蛋白 E 基因敲除小鼠的动脉粥样硬化发展。确定这样的方法将是为易发生动脉粥样硬化的患者开发基于细胞的治疗方法的重要一步。