Denholm E M
Department of Medicine, Albany Medical College, NY 12208-3479.
Am J Pathol. 1992 Oct;141(4):965-71.
It has been shown in previous studies that alveolar macrophages incubated with bleomycin in vitro for 2 to 18 hours secrete monocyte chemotactic factors and fibroblast growth factors (MDGF). The purpose of the current experiments was to determine if alveolar macrophages similarly stimulated with bleomycin would continue to secrete these factors once the stimulus was removed. Alveolar macrophages from normal rats were exposed to bleomycin for 18 hours after which bleomycin was removed and macrophages maintained in culture for 35 days. Conditioned medium (CM) was collected and assayed at weekly intervals. In comparison with nonstimulated controls, bleomycin-stimulated macrophages secreted greater amounts of both monocyte chemotactic factors and MDGF for 35 days after exposure to bleomycin; with a significant difference noted between bleomycin and control macrophages for the first 21 days (P less than 0.02). In agreement with past work, the chemotactic activity in bleomycin-CM was due to fibronectin, as evidenced by the almost complete inhibition of activity by anti-fibronectin antibodies. The time course of secretion of chemotactic and growth factors after a single exposure to bleomycin in vitro was similar to that induced by in vivo exposure of macrophages to this drug. The data suggest that a similar direct activation of macrophages by bleomycin may promote the long-term production of these factors in vivo, resulting in continued monocyte recruitment and promotion of fibroblast proliferation in fibrotic lungs.
以往研究表明,体外与博来霉素孵育2至18小时的肺泡巨噬细胞会分泌单核细胞趋化因子和成纤维细胞生长因子(MDGF)。当前实验的目的是确定经博来霉素类似刺激的肺泡巨噬细胞在去除刺激后是否会继续分泌这些因子。将正常大鼠的肺泡巨噬细胞暴露于博来霉素18小时,之后去除博来霉素,将巨噬细胞在培养中维持35天。每周收集条件培养基(CM)并进行检测。与未刺激的对照相比,博来霉素刺激的巨噬细胞在暴露于博来霉素后35天内分泌的单核细胞趋化因子和MDGF量均更多;在最初21天,博来霉素刺激的巨噬细胞与对照巨噬细胞之间存在显著差异(P小于0.02)。与过去的研究一致,博来霉素-CM中的趋化活性归因于纤连蛋白,抗纤连蛋白抗体几乎完全抑制活性证明了这一点。体外单次暴露于博来霉素后趋化因子和生长因子的分泌时间进程与巨噬细胞体内暴露于该药物所诱导的相似。数据表明,博来霉素对巨噬细胞的类似直接激活可能促进体内这些因子的长期产生,导致纤维化肺中单核细胞持续募集和成纤维细胞增殖。