Hoshino M, Takahashi M, Aoike N
Second Department of Internal Medicine, Toho University School of Medicine, Tokyo, Japan.
J Allergy Clin Immunol. 2001 Feb;107(2):295-301. doi: 10.1067/mai.2001.111928.
Angiogenesis is a prerequisite for airway remodeling in bronchial asthma. Several growth factors may play important roles in inflammation and angiogenesis through effects on inflammatory cell infiltration or neovascularization.
We sought to compare bronchial vascularity and expression of vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and angiogenin in bronchial biopsy specimens from asthmatic and healthy control subjects.
Bronchial biopsy specimens were obtained from 16 asthmatic subjects and 9 normal control subjects. The number of vessel profiles and the vascular area per unit area on a histologic section were estimated by using computerized image analysis after staining for type IV collagen in vessel walls. Numbers of VEGF+, bFGF+, and angiogenin+ cells were determined by means of immunoreactivity.
The airways of asthmatic subjects had significantly more vessels (P < .05) and greater vascular area (P < .001) than that observed in control subjects. Asthmatic subjects exhibited higher VEGF and bFGF and angiogenin immunoreactivity in the submucosa than did control subjects (P < .001, respectively). Significant correlations were detected between the vascular area and the numbers of angiogenic factor-positive cells (VEGF: rs = 0.93, P < .001; bFGF: rs = 0.83, P < .001; angiogenin: rs = 0.88, P < .001) within the asthmatic airways. Furthermore, the degree of vascularity was inversely correlated with airway caliber and airway responsiveness. Colocalization analysis revealed that the angiogenic factor-positive cells were CD34+ cells, eosinophils, and macrophages.
Our results suggest that increased vascularity of the bronchial mucosa in asthmatic subjects is closely related to the expression of angiogenic factors, which may then contribute to the pathogenesis of asthma.
血管生成是支气管哮喘气道重塑的一个先决条件。几种生长因子可能通过对炎症细胞浸润或新血管形成的影响,在炎症和血管生成中发挥重要作用。
我们试图比较哮喘患者和健康对照者支气管活检标本中支气管血管分布以及血管内皮生长因子(VEGF)、碱性成纤维细胞生长因子(bFGF)和血管生成素的表达情况。
从16例哮喘患者和9例正常对照者获取支气管活检标本。在对血管壁IV型胶原染色后,使用计算机图像分析估计组织切片上的血管轮廓数量和单位面积的血管面积。通过免疫反应性确定VEGF+、bFGF+和血管生成素+细胞的数量。
哮喘患者的气道血管数量显著多于对照者(P <.05),血管面积也更大(P <.001)。哮喘患者黏膜下层的VEGF、bFGF和血管生成素免疫反应性高于对照者(分别为P <.001)。在哮喘气道内,血管面积与血管生成因子阳性细胞数量之间存在显著相关性(VEGF:rs = 0.93,P <.001;bFGF:rs = 0.83,P <.001;血管生成素:rs = 0.88,P <.001)。此外,血管化程度与气道管径和气道反应性呈负相关。共定位分析显示,血管生成因子阳性细胞为CD34+细胞、嗜酸性粒细胞和巨噬细胞。
我们的结果表明,哮喘患者支气管黏膜血管化增加与血管生成因子的表达密切相关,这可能进而促成哮喘的发病机制。