Weinstock J V, Blum A M
Cell Immunol. 1984 Nov;89(1):39-45. doi: 10.1016/0008-8749(84)90195-3.
The angiotensin cascade was recently detected in liver granulomas of murine Schistosomiasis mansoni, suggesting an immunoregulatory role for angiotensins in inflammation. In this study, isolated liver granulomas were fractionated into macrophage or lymphocyte-eosinophil-rich populations to determine the cellular origin of these hormones. Immunoreactive angiotensins I, II, and III (AI, AII, and AIII) were detected in granuloma macrophage homogenates by radioimmunoassay and chromatography. No angiotensins were associated with the lymphocyte-eosinophil fraction. Isolated granuloma macrophages, but not the lymphocyte-eosinophil fraction, retained appreciable angiotensins when cultured in vitro and spontaneously released these peptides into the culture medium. Similarly, culture of these cells in the presence of exogenous angiotensinogen or AI resulted in additional AI and/or AII/III appearing in the medium. These data support the contention that granuloma macrophages generate angiotensins from both endogenous and exogenous substrates.
最近在曼氏血吸虫病小鼠的肝脏肉芽肿中检测到血管紧张素级联反应,这表明血管紧张素在炎症中具有免疫调节作用。在本研究中,将分离的肝脏肉芽肿分为富含巨噬细胞或淋巴细胞-嗜酸性粒细胞的群体,以确定这些激素的细胞来源。通过放射免疫分析和色谱法在肉芽肿巨噬细胞匀浆中检测到免疫反应性血管紧张素I、II和III(AI、AII和AIII)。淋巴细胞-嗜酸性粒细胞部分未检测到血管紧张素。分离的肉芽肿巨噬细胞而非淋巴细胞-嗜酸性粒细胞部分,在体外培养时能保留可观的血管紧张素,并将这些肽自发释放到培养基中。同样,在这些细胞存在外源性血管紧张素原或AI的情况下进行培养,会导致培养基中出现额外的AI和/或AII/III。这些数据支持肉芽肿巨噬细胞可从内源性和外源性底物生成血管紧张素这一论点。