Division of Cardiovascular and Diabetes Research, Leeds Institute of Genetics, Health and Therapeutics, and Multidisciplinary Cardiovascular Research Centre, University of Leeds, Leeds, UK.
Br J Surg. 2013 Jun;100(7):895-903. doi: 10.1002/bjs.9128.
Ongoing angiogenesis is implicated in the inflammatory environment that characterizes abdominal aortic aneurysm (AAA). Although lymphangiogenesis has been associated with chronic inflammatory conditions, it has yet to be demonstrated in AAA. The aim was to determine the presence of lymphangiogenesis and to delineate the relationship between inflammation and neovascularization in AAA tissue.
AAA samples and preoperative computed tomography images were obtained from patients undergoing elective AAA repair. Control samples were age-matched abdominal aortic tissue. Specific immunostains for blood vessels (CD31, CD105), lymphatic vessels (D2-40), vascular endothelial growth factor (VEGF) A and VEGF receptor (VEGFR) 3 allowed characterization and quantitation of vasculature.
The AAA wall contained high levels of inflammatory infiltrate; microvascular densities of blood (P < 0·001) and lymphatic (P = 0·003) vessels were significantly increased in AAA samples compared with controls. Maximal AAA vascularity was observed in inflammatory areas, with vessels that stained positively for CD31 (ρ = 0·625, P = 0·017), CD105 (ρ = 0·692, P = 0·009) and D2-40 (ρ = 0·675, P = 0·008) correlating positively with the extent of inflammation. Increased VEGFR-3 and VEGF-A expression was also evident within inflammatory AAA areas.
These findings demonstrated lymphatic vessel involvement in end-stage AAA disease, which was associated with the degree of inflammation, and confirmed the involvement of neovascularization.
持续的血管生成与腹主动脉瘤(AAA)的炎症环境有关。虽然淋巴管生成与慢性炎症有关,但尚未在 AAA 中得到证实。目的是确定淋巴管生成的存在,并描绘 AAA 组织中炎症与新生血管形成之间的关系。
从接受择期 AAA 修复的患者中获得 AAA 样本和术前计算机断层扫描图像。对照样本为年龄匹配的腹主动脉组织。血管(CD31、CD105)、淋巴管(D2-40)、血管内皮生长因子(VEGF)A 和血管内皮生长因子受体(VEGFR)3 的特异性免疫染色允许对血管进行特征描述和定量。
AAA 壁含有高水平的炎症浸润;与对照组相比,AAA 样本中的微血管密度(血液:P < 0·001;淋巴:P = 0·003)明显增加。在炎症区域观察到最大的 AAA 血管生成,与 CD31(ρ = 0·625,P = 0·017)、CD105(ρ = 0·692,P = 0·009)和 D2-40(ρ = 0·675,P = 0·008)阳性染色的血管与炎症程度呈正相关。炎症性 AAA 区域中也明显存在 VEGFR-3 和 VEGF-A 的表达增加。
这些发现表明淋巴管参与终末期 AAA 疾病,与炎症程度有关,并证实了新生血管形成的参与。