Kumar A, Lindner V
Pharmacia and Upjohn, Kalamazoo, Mich, USA.
Arterioscler Thromb Vasc Biol. 1997 Oct;17(10):2238-44. doi: 10.1161/01.atv.17.10.2238.
The ability of gene targeting in the mouse species presents a powerful tool to determine the role of specific molecules in vascular biology. Using a denuding-injury procedure, we recently reported that intimal lesions can be induced in the carotid artery of outbred mice. The technical challenge associated with achieving complete denudation and the relatively small size of the developing lesions prompted us to design the present model of neointima formation and vascular remodeling in the carotid artery of the inbred FVB mouse strain. Complete ligation of the vessel near the carotid bifurcation induced rapid proliferation of medial smooth muscle cells, leading to extensive neointima formation in the presence of an endothelial lining. Thrombus formation was not observed except in the most distal part of the vessel adjacent to the ligature. At 4 weeks after ligation, luminal area was reduced by approximately 80% through a combination of decreased vessel diameter and neointima formation. Ultrastructural analysis provided evidence for cell death in the developing neointima as well as the remodeling media. The present model might be useful in identifying those genes important for neointima formation and vascular remodeling.
在小鼠物种中进行基因靶向的能力为确定特定分子在血管生物学中的作用提供了一个强大的工具。利用去内皮损伤程序,我们最近报道了可在远交系小鼠的颈动脉中诱导内膜损伤。与实现完全去内皮相关的技术挑战以及发育中损伤相对较小的尺寸促使我们设计了目前近交系FVB小鼠品系颈动脉内膜形成和血管重塑的模型。在颈动脉分叉附近对血管进行完全结扎会诱导中膜平滑肌细胞快速增殖,在内皮衬里存在的情况下导致广泛的内膜形成。除了在靠近结扎处的血管最远端部分外,未观察到血栓形成。结扎后4周,通过血管直径减小和内膜形成的共同作用,管腔面积减少了约80%。超微结构分析为发育中的内膜以及重塑的中膜中的细胞死亡提供了证据。目前的模型可能有助于识别那些对内膜形成和血管重塑重要的基因。