Center of Clinical and Translational Sciences, Creighton University School of Medicine, Omaha, NE 68178, USA.
Exp Mol Pathol. 2013 Feb;94(1):45-50. doi: 10.1016/j.yexmp.2012.05.009. Epub 2012 Jun 12.
Neuropeptide Y (NPY) level is elevated in allergic asthmatic airways and activation of NPY receptor-1 (NPY-Y1) on antigen-presenting cells (APCs) is essential for T cell priming. Paradoxically, NPY-Y1 modulates hyper-responsiveness in T cells, suggesting a bimodal role for NPY in APCs and T cells. Therefore, determination of the temporal and spatial expression pattern of NPY and its receptors in asthmatic airways is essential to further understand the role of NPY in allergic asthma.
Lungs were isolated from control and acute and chronic stages of OVA-sensitized and challenged mice (OVA). Stains, including H&E, PAS, and trichrome, were used to determine the severity of lung pathology. The expression patterns of NPY and NPY-Y receptors in the airways were determined using ELISA and immunofluorescence. Cytokine levels in the BALF were also measured.
NPY levels were undetectable in the BALF of control mice, but significantly increased in the OVA group at day 80. Levels of IL-4, TGF-β1 and TGF-β2, significantly increased and peaked on day 45 and decreased on day 80 in the OVA group, exhibiting an inverse correlation with NPY levels. NPY expression was localized to macrophage-like cells in the peri-bronchial and peri-vascular areas in the lung tissue. NPY-Y1 and -Y5 receptors were constitutively expressed by both structural and inflammatory cells in the lung tissue.
NPY produced by activated macrophage-like cells may be involved in regulating cytokine production and cellular activities of immune cells in asthma. However, it remains unclear whether such an increase in NPY is a defensive/compensatory mechanism to modulate the effects of inflammatory cytokines.
神经肽 Y(NPY)在过敏性哮喘的气道中升高,抗原呈递细胞(APC)上的 NPY 受体-1(NPY-Y1)的激活对于 T 细胞的启动是必不可少的。矛盾的是,NPY-Y1 调节 T 细胞的高反应性,这表明 NPY 在 APC 和 T 细胞中具有双重作用。因此,确定 NPY 及其受体在哮喘气道中的时空表达模式对于进一步了解 NPY 在过敏性哮喘中的作用至关重要。
从对照和 OVA 敏化和挑战的急性和慢性阶段的小鼠(OVA)中分离肺。使用 H&E、PAS 和三色染色来确定肺病理学的严重程度。使用 ELISA 和免疫荧光法确定气道中 NPY 和 NPY-Y 受体的表达模式。还测量了 BALF 中的细胞因子水平。
对照小鼠的 BALF 中无法检测到 NPY,但 OVA 组在第 80 天显着增加。OVA 组中 IL-4、TGF-β1 和 TGF-β2 的水平显着增加,并在第 45 天达到峰值,然后在第 80 天下降,与 NPY 水平呈负相关。NPY 表达定位于肺组织中支气管周围和血管周围区域的巨噬细胞样细胞中。NPY-Y1 和 -Y5 受体在肺组织中的结构细胞和炎症细胞中均持续表达。
活化的巨噬细胞样细胞产生的 NPY 可能参与调节哮喘中细胞因子的产生和免疫细胞的细胞活性。然而,尚不清楚 NPY 的这种增加是否是一种防御/代偿机制,以调节炎症细胞因子的作用。