Daugherty Alan, Cassis Lisa A
Department of Medicine, Gill Heart Institute, University of Kentucky, Lexington, KY 40536-0230, USA.
Arterioscler Thromb Vasc Biol. 2004 Mar;24(3):429-34. doi: 10.1161/01.ATV.0000118013.72016.ea. Epub 2004 Jan 22.
Many mouse models of abdominal aortic aneurysms have been developed that use a diverse array of methods for producing the disease, including genetic manipulation and chemical induction. These models could provide insight into potential mechanisms in the development of this disease. Although experimental studies on abdominal aortic aneurysms (AAAs) have used a variety of mammalian and avian approaches, there is an increasing reliance on the use of mice. The models recapitulate some facets of the human disease including medial degeneration, inflammation, thrombus formation, and rupture. Most of the mouse models of AAA are evoked either by genetically defined approaches or by chemical means. The genetic approaches are spontaneous and engineered mutations. These include defects in extracellular matrix maturation, increased degradation of elastin and collagen, aberrant cholesterol homeostasis, and enhanced production of angiotensin peptides. The chemical approaches include the intraluminal infusion of elastase, periaortic incubations of calcium chloride, and subcutaneous infusion of AngII. A common feature of these models is the reduction of AAA incidence and severity by the prophylactic administration of matrix metalloproteinase (MMP) inhibitors or genetically engineered deficiencies of specific members of this proteolytic protein family. The validation of mouse models of AAAs will provide insight into the mechanisms of progression of the human disease.
已经开发出许多腹主动脉瘤的小鼠模型,这些模型使用了多种引发该疾病的方法,包括基因操作和化学诱导。这些模型可以为这种疾病发展的潜在机制提供见解。尽管关于腹主动脉瘤(AAA)的实验研究使用了多种哺乳动物和禽类方法,但对小鼠的使用依赖度正在增加。这些模型概括了人类疾病的一些方面,包括中膜退变、炎症、血栓形成和破裂。大多数AAA小鼠模型是通过基因定义的方法或化学方法诱发的。基因方法包括自发突变和工程突变。这些包括细胞外基质成熟缺陷、弹性蛋白和胶原蛋白降解增加、异常的胆固醇稳态以及血管紧张素肽产生增加。化学方法包括腔内注入弹性蛋白酶、主动脉周围氯化钙孵育以及皮下注入血管紧张素II。这些模型的一个共同特征是通过预防性给予基质金属蛋白酶(MMP)抑制剂或该蛋白水解蛋白家族特定成员的基因工程缺陷来降低AAA的发生率和严重程度。AAA小鼠模型的验证将为人类疾病进展的机制提供见解。