Department of Radiology, Stanford University School of Medicine, Palo Alto, CA 94304, USA.
Curr Med Chem. 2013;20(9):1127-46. doi: 10.2174/0929867311320090003.
Islet transplantation is an attractive strategy to treat severe diabetic conditions in patients suffering from autoimmune derived diabetes, and it has currently been considered a forefront research arena in diabetes. Major aim of islet transplantation is to achieve successful insulin independent disease free survival. The key challenges in transplanted islets are the generation of reactive oxygen species (ROS) and associated oxidative stress, pro-inflammatory cytokine - (TNFα) mediated apoptotic induction, attack by immune cells, and achieving revascularization with minimal hypoxic microenvironment. Free radicals and their derivatives are constantly produced in living systems, but at relatively low level, and in a balanced state. Oxidative stress, which occurs as a result of an imbalance between the intracellular free radicals production and the cellular antioxidant defense mechanisms in the transplanted islets, can lead to cell death. The balance between oxidants and antioxidants in a cell can be easily disturbed by increase in ROS production or reduction in the level of cellular antioxidant defensive substances, which can cause many metabolic complications, including pancreatic β-cell damage. Antioxidants function as blockers of radical processes by eliminating harmful ROS produced during normal cellular metabolism. A complex antioxidant defense mechanism has been developed by nature in cells to protect the cellular homeostasis. This system mainly includes antioxidant enzymes, vitamins and minerals. As transplanted islet survival is crucial for achieving successful therapy, most of these antioxidants can be used as a supplement to scavenge the local ROS thereby improving the survival of transplanted islets. Currently, very few techniques have been routinely used to qualitatively and quantitatively assess the survival and function of islet grafts, especially to confirm the success of treatment, which includes metabolic parameters such as blood glucose, insulin and C-peptide levels. These biochemical measurements provide markers at only the late stages of islet rejection. Use of molecular imaging techniques has the potential for real-time non-invasive monitoring of the functional status and viability of transplanted islet grafts in living animals. This review mainly focuses on the current status of islet transplantations, potential preventive strategies used to reduce oxidative stress-mediated toxicity in islet grafts, and use of molecular imaging as a tool to quantitatively evaluate the functional status of the transplanted islets in living animals.
胰岛移植是治疗自身免疫性糖尿病患者严重糖尿病的一种有吸引力的策略,目前已被认为是糖尿病研究的前沿领域。胰岛移植的主要目的是实现成功的胰岛素非依赖性、无疾病生存。移植胰岛的关键挑战是活性氧(ROS)的产生和相关的氧化应激、促炎细胞因子(TNFα)介导的凋亡诱导、免疫细胞的攻击以及在最小缺氧微环境中实现再血管化。自由基及其衍生物在活细胞中不断产生,但水平相对较低,且处于平衡状态。氧化应激是由于移植胰岛中细胞内自由基产生与细胞抗氧化防御机制之间的不平衡引起的,可导致细胞死亡。细胞内氧化剂和抗氧化剂之间的平衡很容易被 ROS 产生的增加或细胞抗氧化防御物质水平的降低所扰乱,这可能导致许多代谢并发症,包括胰岛β细胞损伤。抗氧化剂通过消除正常细胞代谢过程中产生的有害 ROS 来作为自由基过程的阻断剂。细胞中已经开发出一种复杂的抗氧化防御机制来保护细胞内稳态。该系统主要包括抗氧化酶、维生素和矿物质。由于移植胰岛的存活对于实现成功的治疗至关重要,因此大多数抗氧化剂可用作清除局部 ROS 的补充剂,从而提高移植胰岛的存活率。目前,很少有技术被常规用于定性和定量评估胰岛移植物的存活和功能,特别是要确认治疗的成功,这包括代谢参数,如血糖、胰岛素和 C 肽水平。这些生化测量仅提供胰岛排斥的晚期标志物。使用分子成像技术有可能实时非侵入性监测活动物中移植胰岛移植物的功能状态和活力。本综述主要关注胰岛移植的现状、用于减少胰岛移植物中氧化应激介导毒性的潜在预防策略,以及使用分子成像作为工具来定量评估活动物中移植胰岛的功能状态。